Plant Comparison

Hemp vs Devil's Claw

A side-by-side comparison of two medicinal plants — every documented constituent, action, use, safety note and cited source, assembled automatically from the Omnia Sana database.

First plant
Second plant
Show:
Plant AHempCannabis sativaCannabaceaeFull monograph →
Plant BDevil's ClawHarpagophytum procumbensPedaliaceaeFull monograph →

At a glance

Hemp and Devil's Claw: they share 6 indicated uses (arthritis / joint pain, back pain, headache, …); 2 pharmacological actions in common.

HempDevil's Claw
Constituents32
Pharmacological actions42
Indicated uses86
Safety notes23
Cited sources1915
Indicated uses
Only Hemp
Cardiovascular / heart healthInsomnia / sleeplessness
Shared (6)
Arthritis / joint painBack painHeadacheInflammation (general)Pain (general)Skin irritation
Only Devil's Claw
none
Pharmacological actions
Only Hemp
AntioxidantSedative / sleep support
Shared (2)
Analgesic (pain relief)Anti-inflammatory
Only Devil's Claw
none

Evidence face-off — shared uses

ConditionHempDevil's ClawVerdict
Arthritis / joint pain5/108/10Stronger for Devil's Claw
Back pain5/109/10Stronger for Devil's Claw
Headache5/108/10Stronger for Devil's Claw
Inflammation (general)5/108/10Stronger for Devil's Claw
Pain (general)5/109/10Stronger for Devil's Claw
Skin irritation5/108/10Stronger for Devil's Claw

Evidence scores (1–10) are computed from the tier of each cited source. “Comparable” means the two scores are within one point. Follow a score to its detailed sources.

Key Constituents

Cannabinoids (THC, CBD and related compounds)[14, 15]

The characteristic bioactive compounds of the resin-bearing flowers, varying widely in ratio and concentration between cultivars; THC is psychoactive, CBD is not.

Terpenes[14]

Aromatic terpenes contribute to the plant's characteristic scent and may modulate cannabinoid effects.

Terpenes / terpenoidsEssential (volatile) oil
Seed oil fatty acids[14]

Hemp seed is rich in polyunsaturated fatty acids (including omega-3 and omega-6), giving the pressed seed oil its nutritional value; essentially free of psychoactive cannabinoids.

Iridoid glycosides (harpagoside, harpagide, procumbide)[12, 13, 14]

Harpagoside is the main marker compound and anti-inflammatory principle; effective extracts are standardised to it, with the better-quality clinical evidence using preparations delivering roughly 50-60 mg harpagoside per day.

Iridoid glycosidesHarpagosideGlycosides
Phenylethanoids (acteoside/verbascoside) and flavonoids[13]

Antioxidant supporting constituents.

Verbascoside (acteoside)Flavonoids

Pharmacological Actions

Analgesic (pain relief)[1, 7, 9, 12, 14, 15, 16]
Anti-inflammatory[6, 8, 10, 12, 14, 15, 16]
Antioxidant[5, 14, 15, 16]
Sedative / sleep support[14, 15, 16]
Analgesic (pain relief)[1, 2, 4, 6, 7, 9, 10, 12, 13]

Anti-inflammatory and analgesic for osteoarthritis (hip and knee) pain

Anti-inflammatory[1, 3, 4, 5, 6, 8, 9, 11, 12, 13]

Anti-inflammatory and analgesic for osteoarthritis (hip and knee) pain

Traditional & Indicated Uses

Arthritis / joint pain[14, 15, 16]Moderate · 5/10

inferred from anti-inflammatory action

Evidence: 5
Label: Arthritis / joint pain
Back pain[14, 15, 16]Moderate · 5/10

inferred from analgesic action

Evidence: 5
Label: Back pain
Cardiovascular / heart health[14, 15, 16]Moderate · 5/10
Evidence: 5
Label: Cardiovascular / heart health
Headache[14, 15, 16]Moderate · 5/10

inferred from analgesic action

Evidence: 5
Label: Headache
Inflammation (general)[14, 15, 16]Moderate · 5/10

inferred from anti-inflammatory action

Evidence: 5
Label: Inflammation (general)
Insomnia / sleeplessness[14, 15, 16]Moderate · 5/10

inferred from sedative action

Evidence: 5
Label: Insomnia / sleeplessness
Pain (general)[14, 15, 16]Moderate · 5/10
Evidence: 5
Label: Pain (general)
Skin irritation[14, 15, 16]Moderate · 5/10

inferred from anti-inflammatory action

Evidence: 5
Label: Skin irritation
Arthritis / joint pain[12, 13]Good · 8/10

Anti-inflammatory and analgesic for osteoarthritis (hip and knee) pain; General joint pain and arthritis support

Evidence: 8
Label: Arthritis / joint pain
Back pain[12, 13, 14, 15]Strong · 9/10

Effective at standardised doses (~50-60 mg harpagoside/day); an aqueous extract was non-inferior to rofecoxib for short-term chronic low back pain; Relief of chronic non-specific low back pain

Evidence: 9
Label: Back pain
Headache[12, 13]Good · 8/10

inferred from analgesic action

Evidence: 8
Label: Headache
Inflammation (general)[12, 13]Good · 8/10

inferred from anti-inflammatory action

Evidence: 8
Label: Inflammation (general)
Pain (general)[12, 13, 14, 15]Strong · 9/10

Anti-inflammatory and analgesic for osteoarthritis (hip and knee) pain; Effective at standardised doses (~50-60 mg harpagoside/day); an aqueous extract was non-inferior to rofecoxib for short-term chronic low back pain; General joint pain and arthritis support; Relief of chronic non-specific low back pain

Evidence: 9
Label: Pain (general)
Skin irritation[12, 13]Good · 8/10

inferred from anti-inflammatory action

Evidence: 8
Label: Skin irritation

Safety, Cautions & Contraindications

Safety note[14, 15, 16]Caution

Industrial hemp (low-THC cannabis) seed oil and seeds are generally safe as food. CBD products derived from hemp may interact with medications metabolised by cytochrome P450 liver enzymes, including common anticoagulants, antiepileptics, and immunosuppressants. THC-containing preparations impair driving and are regulated or prohibited in many jurisdictions. Not recommended during pregnancy or breastfeeding. Quality and cannabinoid content vary widely between hemp products.

Safety note[14, 15, 16, 17]Caution

Duke (2002) rates cannabis as ++ and notes clinical evidence (score 2) for its antiemetic activity, especially relevant for chemotherapy-induced nausea. Score 1 activities include analgesic, anticonvulsant, and anti-inflammatory properties. Duke highlights the legal and pharmacological complexity, noting THC as the primary psychoactive compound. Medically, synthetic cannabinoids (dronabinol, nabilone) are clinically approved for nausea and anorexia. Duke cautions that while the plant has genuine therapeutic potential, psychoactive effects, legal restrictions, and risk of dependence with regular use must be considered (Duke, 2002).

Safety note[13]Caution

Because it is a bitter that increases stomach-acid and bile secretion, it is contraindicated in active peptic ulcer, gastritis and (without medical supervision) gallstones.

Safety note[13]Caution

May add to the effect of anticoagulants (e.g. warfarin) and may influence blood sugar, blood pressure and heart rhythm; use caution with these medicines.

Safety note[13]Caution

Avoid during pregnancy (oxytocic/uterine effect) and while breastfeeding.

External Ids

Gbif: 5361880
Wikidata: Q26726
Gbif: 3585335
Powo: urn:lsid:ipni.org:names:675824-1
Wikidata: Q386675

Botanical Description

Erect annual herb with a distinctive palmately compound leaf of narrow, serrated leaflets. The plant is usually dioecious (separate male and female plants); female plants develop dense, resinous flower clusters, while male plants bear looser pollen-releasing flowers. The seed (achene) is small, hard-shelled and oil-rich.[14]

Height: 1-5 m, depending on variety and cultivation
Habit: Erect, fast-growing annual herb
Leaves: Palmately compound, narrow serrated leaflets
Flowers: Dioecious; female flowers in dense resinous clusters, male flowers looser and pollen-releasing
Stem: Erect, fibrous, often ridged
Root: Taproot with fibrous lateral roots
Fruit: Small, hard-shelled, oil-rich achene (seed)
Flowering Period: Late summer to autumn

Low-growing, sprawling perennial herb with trailing stems and deeply lobed, greyish-green leaves arising from a large, fleshy primary taproot bearing smaller secondary storage tubers (the part used medicinally). Striking funnel-shaped, purplish-pink to violet flowers give way to a distinctive woody fruit covered in long, hooked spines - the origin of the common name.[13]

Height: Trailing stems to 1.5 m, low-growing
Habit: Low-growing, sprawling perennial herb
Leaves: Deeply lobed, greyish-green
Flowers: Funnel-shaped, purplish-pink to violet
Stem: Trailing, sprawling stems
Root: Large primary taproot with smaller secondary storage tubers (the medicinal part)
Fruit: Woody capsule covered in long, hooked spines ('devil's claw')
Flowering Period: Summer (during the rainy season)

Habitat

Believed native to Central Asia; now cultivated worldwide, with industrial hemp (low-THC cultivars) grown in temperate climates for fibre, seed and cannabinoid extraction, subject to varying legal regulation by jurisdiction.[14]

Native to the dry savannas and semi-desert regions of southern Africa, particularly the Kalahari Desert region of Namibia, Botswana and South Africa.[13]

Harvesting

Flowers (and resin-bearing leaves) are harvested at peak resin/cannabinoid content, typically as the flower clusters mature in late summer to autumn; seed is harvested once mature and dried, then pressed for oil or used whole.[14]

Parts: Flower, Leaf, Seed
Season: Late summer to autumn

The secondary root tubers are dug by hand, sliced and dried in the sun, traditionally by local harvesters in southern Africa; sustainable wild-harvesting practices are important given the plant's slow growth and habitat sensitivity.

Parts: Secondary root tuber

Traditional Uses

Cannabis/hemp has a long multi-cultural history as a fibre, food and medicinal plant, traditionally used for pain, muscle spasm, sleep and appetite, alongside industrial use of the fibre and seed. Modern cannabinoid research, particularly on THC and CBD, has substantially expanded the evidence base for pain, spasticity and specific seizure disorders.[14, 15]

Devil's claw has a long southern African traditional-medicine history as a remedy for fever, pain and digestive complaints, and is now one of the most clinically studied herbal analgesics for osteoarthritis and chronic low back pain, with standardised extracts showing efficacy comparable to some conventional analgesics in trials.[13]

Preparations

Seed / seed oil[14]

Whole or hulled seed, or cold-pressed seed oil, used as a nutritional food source (essentially free of psychoactive cannabinoids).

Standardised cannabinoid extract[15]

Extract standardised to specific cannabinoid content (e.g. CBD), used in regulated medicinal products; regulatory status varies widely by jurisdiction and product type.

Standardised extract[13, 14]

Root tuber extract standardised to harpagoside content, taken as capsules or tablets; the best-studied clinical form for osteoarthritis and back pain.

References

REF-0758, REF-0759, REF-0760, REF-2132, REF-2133, REF-2134, REF-2135, REF-2136, REF-2137, REF-2138, REF-2139, REF-2140, REF-2141
REF-1829, REF-1830, REF-1831, REF-1832, REF-1833, REF-1834, REF-1835, REF-1836, REF-1837, REF-1838, REF-1839

Drug Class Interactions

Safety note[18, 19]Caution
Drug Class: sedatives-cns-depressants
Mechanism: Cannabis (and CBD) commonly cause drowsiness and sedation; taken with sedatives, sleeping tablets, opioids or other central-nervous-system depressants (including alcohol) it may add to drowsiness and slowed reactions.
Reviewed By: Omnia Sana (owner-authorized)
Reviewed Date: 2026-07-03
Safety note[18]Caution
Drug Class: anticonvulsants
Mechanism: Cannabidiol (CBD) interacts with anti-seizure medicines - notably raising exposure to clobazam - and can add to sedation; anyone combining cannabis/CBD with anticonvulsants should be monitored and doses reviewed by their clinician.
Reviewed By: Omnia Sana (owner-authorized)
Reviewed Date: 2026-07-03

Not documented

Lookalikes Review

Outcome: none-known
Reviewed By: Omnia Sana (owner-authorized)
Reviewed Date: 2026-07-07
Outcome: none-known
Reviewed By: Omnia Sana (owner-authorized)
Reviewed Date: 2026-07-07

Dosage

Not documented

Standardised extract[14]

Clinical trials for osteoarthritis and back pain commonly use extracts providing around 50-60 mg harpagoside daily. Educational reference only, not a prescription.

References & Sources

  1. Rock, E.M. and Parker, L.A (2021) 'Constituents of Cannabis sativa', Advances in Experimental Medicine and Biology, 1264, pp. 1-13. doi:10.1007/978-3-030-57369-0_1 Traditional / reference
    https://doi.org/10.1007/978-3-030-57369-0_1
  2. Castillo-Arellano, J., Canseco-Alba, A., Cutler, S.J. and León, F (2023) 'The Polypharmacological Effects of Cannabidiol', Molecules, 28(7), pp. 3271. doi:10.3390/molecules28073271 Traditional / reference
    https://doi.org/10.3390/molecules28073271
  3. Pagano, C., Navarra, G., Coppola, L., Avilia, G. et al (2022) 'Cannabinoids: Therapeutic Use in Clinical Practice', International Journal of Molecular Sciences, 23(6), pp. 3344. doi:10.3390/ijms23063344 Traditional / reference
    https://doi.org/10.3390/ijms23063344
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  9. Liktor-Busa, E., Keresztes, A., LaVigne, J., Streicher, J.M. and Largent-Milnes, T.M (2021) 'Analgesic potential of terpenes derived from Cannabis sativa', Pharmacological Reviews, 73(4), pp. 98-126. doi:10.1124/pharmrev.120.000046 Meta-analysis / review
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  10. Martinelli, G., Magnavacca, A., Fumagalli, M., Dell'Agli, M., Piazza, S. and Sangiovanni, E (2021) 'Cannabis sativa and skin health: dissecting the role of phytocannabinoids', Planta Medica, 88(7), pp. 492-506. doi:10.1055/a-1420-5780 Meta-analysis / review
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  11. Andre, C.M., Hausman, J.F. and Guerriero, G (2016) 'Cannabis sativa: the plant of the thousand and one molecules', Frontiers in Plant Science, 7, pp. 19. doi:10.3389/fpls.2016.00019 Meta-analysis / review
    https://doi.org/10.3389/fpls.2016.00019
  12. Bonini, S.A., Premoli, M., Tambaro, S., Kumar, A., Maccarinelli, G., Memo, M. and Mastinu, A (2018) 'Cannabis sativa: a comprehensive ethnopharmacological review of a medicinal plant with a long history', Journal of Ethnopharmacology, 227, pp. 300-315. doi:10.1016/j.jep.2018.09.004 Meta-analysis / review
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  13. Bergamaschi, M.M., Queiroz, R.H.C., Zuardi, A.W. and Crippa, J.A.S (2011) 'Safety and side effects of cannabidiol, a Cannabis sativa constituent', Current Drug Safety, 6(4), pp. 237-249. doi:10.2174/157488611798280924 Meta-analysis / review
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  14. Cerino, P., Buonerba, C., Cannazza, G. et al (2021) 'A review of hemp as food and nutritional supplement', 6(1), pp. 19--27. doi:10.1089/can.2020.0001 Preclinical
    https://doi.org/10.1089/can.2020.0001
  15. Devinsky, O., Cross, J.H., Laux, L. et al (2017) 'Trial of cannabidiol for drug-resistant seizures in the Dravet syndrome', 376(21), pp. 2011--2020. Randomized trial
    https://scholar.google.com/scholar?q=Trial%20of%20cannabidiol%20for%20drug-resistant%20seizures%20in%20the%20Dravet%20syndrome
  16. Royal Botanic Gardens, Kew (n.d.). Available at: https://powo.science.kew.org Traditional / reference
    https://powo.science.kew.org
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    https://scholar.google.com/scholar?q=Handbook%20of%20Medicinal%20Herbs%2C%20Second%20Edition
  18. Talwar, A., Estes, E., Aparasu, R. and Reddy, D.S (2022) 'Clinical efficacy and safety of cannabidiol for pediatric refractory epilepsy indications: A systematic review and meta-analysis', Experimental Neurology, 359, pp. 114238. doi:10.1016/j.expneurol.2022.114238 Meta-analysis / review
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  19. Caus, M.N., Lupoae, M. and Chitescu, C.L (2026) 'Efficacy and Safety of Herbal Supplements with Anxiolytic, Antidepressant, and Sedative Action: A Review of Clinical Data and Toxicological Risks', Pharmaceuticals, 19(3), pp. 399. doi:10.3390/ph19030399 Meta-analysis / review
    https://doi.org/10.3390/ph19030399
  1. Mncwangi, N., Chen, W., Vermaak, I., Viljoen, A.M. and Gericke, N (2012) 'Devil's Claw - a review of the ethnobotany, phytochemistry and biological activity of Harpagophytum procumbens', Journal of Ethnopharmacology, 143(3), pp. 755-771. doi:10.1016/j.jep.2012.08.013 Meta-analysis / review
    https://doi.org/10.1016/j.jep.2012.08.013
  2. Parenti, C., Arico, G., Pennisi, M., Venditti, A. and Scoto, G.M (2015) 'Harpagophytum procumbens extract potentiates morphine antinociception in neuropathic rats', Natural Product Research, 30(11), pp. 1248-1255. doi:10.1080/14786419.2015.1052069 Preclinical
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  3. Mariano, A., Bigioni, I., Mattioli, R., Di Sotto, A., Leopizzi, M., Garzoli, S., Mariani, P.F., Dalla Vedova, P., Ammendola, S. and Scotto d'Abusco, A (2022) 'Harpagophytum procumbens Root Extract Mediates Anti-Inflammatory Effects in Osteoarthritis Synoviocytes through CB2 Activation', Pharmaceuticals, 15(4), pp. 457. doi:10.3390/ph15040457 Preclinical
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  5. Menghini, L., Recinella, L., Leone, S., Chiavaroli, A., Cicala, C., Brunetti, L., Vladimir-Knezevic, S., Orlando, G. and Ferrante, C (2019) 'Devil's claw (Harpagophytum procumbens) and chronic inflammatory diseases: A concise overview on preclinical and clinical data', Phytotherapy Research, 33(9), pp. 2152-2162. doi:10.1002/ptr.6395 Meta-analysis / review
    https://doi.org/10.1002/ptr.6395
  6. Brien, S., Lewith, G.T. and McGregor, G (2006) 'Devil's Claw (Harpagophytum procumbens) as a treatment for osteoarthritis: a review of efficacy and safety', Journal of Alternative and Complementary Medicine, 12(10), pp. 981-993. doi:10.1089/acm.2006.12.981 Meta-analysis / review
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  7. Ungerer, G., Cui, J., Ndam, T., Bekemeier, M., Song, H., Li, R., Siedhoff, H.R., Yang, B., Appenteng, M.K., Greenlief, C.M., Miller, D.K., Sun, G.Y., Folk, W.R. and Gu, Z (2020) 'Harpagophytum procumbens Extract Ameliorates Allodynia and Modulates Oxidative and Antioxidant Stress Pathways in a Rat Model of Spinal Cord Injury', Neuromolecular Medicine, 22(2), pp. 278-292. doi:10.1007/s12017-019-08585-z Preclinical
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  8. Recinella, L., Chiavaroli, A., Ronci, M., Menghini, L., Brunetti, L., Leone, S., Tirillini, B., Angelini, P., Covino, S., Venanzoni, R., Zengin, G., Di Simone, S., Ciferri, M.C., di Giacomo, V., Cataldi, A., Rapino, M., Valerio, V.D., Orlando, G. and Ferrante, C (2020) 'Multidirectional Pharma-Toxicological Study on Harpagophytum procumbens DC. ex Meisn.: An IBD-Focused Investigation', Antioxidants, 9(2), pp. 168. doi:10.3390/antiox9020168 Preclinical
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  11. Jang, M., Lim, S., Han, S., Park, H., Shin, I., Kim, J., Kim, N., Lee, J., Kim, K. and Kim, C (2003) 'Harpagophytum procumbens suppresses lipopolysaccharide-stimulated expressions of cyclooxygenase-2 and inducible nitric oxide synthase in fibroblast cell line L929', Journal of Pharmacological Sciences, 93(3), pp. 367-371. doi:10.1254/jphs.93.367 Preclinical
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  12. Chrubasik, S (2004) 'Devil's claw extract as an example of the effectiveness of herbal analgesics', Der Orthopade. doi:10.1007/s00132-004-0675-7 Clinical study
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  13. Brendler, T., Gruenwald, J., Ulbricht, C. and Basch, E (2006) 'Devil's Claw (Harpagophytum procumbens DC): an evidence-based systematic review by the Natural Standard Research Collaboration', Journal of Herbal Pharmacotherapy. doi:10.1080/j157v06n01_09 Meta-analysis / review
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  14. Chrubasik, S., Conradt, C. and Roufogalis, B.D (2004) 'Effectiveness of Harpagophytum extracts and clinical efficacy', Phytotherapy Research, 18(2), pp. 187--189. doi:10.1002/ptr.1416 Preclinical
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Generated automatically from the Omnia Sana plant database and its cited sources. For educational purposes only — not medical advice. Always consult a qualified practitioner before using medicinal plants.