Chanca piedra (Phyllanthus niruri, gale of the wind)
Also called Phyllanthus niruri, gale of the wind, stonebreaker, stone breaker, quebra-pedra, seed-under-leaf.
Best grade B across 8 graded outcomes Botanical Last checked
The short answer
From 12 sourcesChanca piedra (Phyllanthus niruri) is the most common ingredient in kidney-stone supplements, but controlled evidence is limited: in a 69-person trial it changed urinary calcium only in people with high calcium and did not improve stone passage. Liver trials were mostly null on their main outcomes, and a placebo-controlled hepatitis B trial was stopped for lack of benefit. Short-term safety looks acceptable.
Every graded outcome on this page
8 rows · line = participants- BGrade BLiver fat, liver enzymes and fibrosis score in fatty liverLivern 226
- CGrade CHepatitis B virus markersHepatitis Bn 1,326
- CGrade CStone clearance after shock-wave lithotripsyKidney stonesn 150
- CGrade CLiver enzymes and fibrosis score with a P. niruri and milk thistle combinationLivern 128
- CGrade CLiver function in alcoholic hepatitisLivern 71
- CGrade CUrine chemistry and stone passage in calcium stone formersKidney stonesn 69
- DGrade DUrine chemistry and stone eliminationKidney stonesn 56
- DGrade DHepatitis B viral loadHepatitis Bn 47
- 5 more graded outcomes, in the evidence chapter
Key facts
- Kidney stones
- In 69 calcium stone formers, 3 months of P. niruri did not change urine chemistry overall or stone passage versus placebo; urinary calcium fell only in the subgroup with high urinary calcium1
- After lithotripsy
- In 150 people who had shock-wave lithotripsy, 2 g/day gave a 93.5% vs 83.3% stone-free rate at 180 days (not significant overall); the authors report a benefit for lower-pole stones11
- Stone size
- A meta-analysis found only two controlled studies, with modest reductions in stone size and number6
- Fatty liver
- 3,000 mg/day for 12 months did not lower liver fat (CAP score) or liver enzymes versus placebo in 226 adults, though the fibrosis score improved3
- Hepatitis B
- A Cochrane review found no convincing evidence of benefit versus placebo, and a 12-month placebo-controlled trial was stopped for lack of benefit52
- Oxalate content
- A laboratory analysis of kidney-stone supplements measured 8.2 mg of oxalate per dose of chanca piedra8
What it is
Chanca piedra is the herb Phyllanthus niruri, also called gale of the wind or stonebreaker, sold mainly for kidney stones and liver health.
How it works
ProposedReviews of laboratory and animal work describe P. niruri interfering with calcium oxalate crystal formation and growth and promoting glycosaminoglycan aggregation; in small human studies urinary calcium, oxalate and uric acid fell in subgroups with high levels. These are proposed mechanisms, not confirmed clinical effects.917
Forms, side by side
2 forms named in our sources. The rest show what our data holds, and say plainly where it holds nothing yet.
Chanca piedra (Phyllanthus niruri, gale of the wind) forms compared
2 forms| 2 forms | Dried herb or extract capsules | Herbal tea (infusion) |
|---|---|---|
| Absorption in people | No human absorption data.1 | Not measured.7 |
| GI tolerance | No major adverse events at 3,000 mg/day for 12 months; kidney function unchanged in a 12-month hepatitis B trial.32 | Supplements were measured to contain 8.2 mg oxalate per dose; teas were not tested for oxalate. The uncontrolled infusion study reported no significant adverse effects.87 |
| Studied for | Kidney stones, fatty liver, hepatitis B | Traditional kidney-stone use; one uncontrolled 12-week study of an infusion in stone formers |
- Dried herb or extract capsules
- Herbal tea (infusion)
- Absorption in people
- Not measured.7
- GI tolerance
- Supplements were measured to contain 8.2 mg oxalate per dose; teas were not tested for oxalate. The uncontrolled infusion study reported no significant adverse effects.87
- Studied for
- Traditional kidney-stone use; one uncontrolled 12-week study of an infusion in stone formers
What the human research says
Human trials only, one row per outcome. The form line shows what each trial actually tested. Grades follow our evidence-grading policy.
Trial map
8 graded outcomes, largest study first8 graded outcomes: 1 improved, 5 mixed, 2 no effect. The largest, a 2011 meta-analysis of 1,326 people on hepatitis B virus markers, found mixed results.
1Hepatitis B virus markers
Mixed · Grade C · Meta-analysis, 1,326 people, 2011
People with chronic hepatitis B in randomized trials (mostly China)
Dose, result and source| Outcome | Found | People | Study | Who was studied |
|---|---|---|---|---|
| Hepatitis B virus markers | Mixed | 1,326 | Grade C · Meta-analysis, 2011 | People with chronic hepatitis B in randomized trials (mostly China) |
| Liver fat, liver enzymes and fibrosis score in fatty liver | Mixed | 226 | Grade B · RCT, 2023 | Malaysian adults with mild-to-moderate non-alcoholic fatty liver disease |
| Stone clearance after shock-wave lithotripsy | Mixed | 150 | Grade C · RCT, 2006 | Italian adults with calcium oxalate kidney stones up to 25 mm treated with shock-wave lithotripsy |
| Liver enzymes and fibrosis score with a P. niruri and milk thistle combination | No effect | 128 | Grade C · RCT, 2025 | Egyptian adults with risk factors for non-alcoholic steatohepatitis (146 enrolled) |
| Liver function in alcoholic hepatitis | Mixed | 71 | Grade C · RCT, 2021 | Indian adults with mild-to-moderate alcoholic hepatitis |
| Urine chemistry and stone passage in calcium stone formers | Mixed | 69 | Grade C · RCT, 2004 | Brazilian adults who form calcium kidney stones |
| Urine chemistry and stone elimination | Improved | 56 | Grade D · Open-label trial, 2018 | Brazilian adults with kidney stones under 10 mm |
| Hepatitis B viral load | No effect | 47 | Grade D · RCT, 2018 | Adults with chronic hepatitis B |
Every graded row
8 rowsShowing 8 of 8 outcomes. Human trials only.
BGrade BLiver fat, liver enzymes and fibrosis score in fatty liverLiverPrimary outcomes not metRCT
n 226 · 2023
Mixed No difference from placebo in liver fat (CAP -15.05 vs -14.74 dB/m) or liver enzymes, the primary outcomes. Fibrosis score fell with the extract (-0.64 vs +0.10 kPa). No major adverse events.
- Design
- RCT, n = 226, 2023
- Population
- Malaysian adults with mild-to-moderate non-alcoholic fatty liver disease
- Form
- Standardized P. niruri extract
- Dose
- 3,000 mg/day
- Duration
- 12 months
- Source
- Reference 3 · PubMed 37313177 (opens PubMed)
CGrade CHepatitis B virus markersHepatitis BNo convincing benefit vs placeboMeta-analysis · 16 studies
n 1,326 · 2011
Mixed Versus placebo (one trial, 42 people) there was no difference in HBeAg seroconversion. Added to antivirals, Phyllanthus improved HBV DNA and HBeAg measures, but with substantial heterogeneity and risk of bias; no serious adverse events were reported.
- Design
- Meta-analysis, 16 studies, n = 1,326, 2011
- Population
- People with chronic hepatitis B in randomized trials (mostly China)
- Form
- Phyllanthus species, alone or added to antiviral drugs
- Dose
- Varied by trial
- Duration
- Varied by trial
- Source
- Reference 5 · PubMed 21491412 (opens PubMed)
CGrade CStone clearance after shock-wave lithotripsyKidney stonesNo overall difference; lower-pole benefitRCT
n 150 · 2006
Mixed Stone-free rate at 180 days was 93.5% with P. niruri vs 83.3% in untreated controls (p = 0.48 overall); the authors report a significant benefit for lower-pole (lower caliceal) stones. Re-treatment was needed in 39.7% vs 43.3%. No side effects were recorded.
- Design
- RCT, n = 150, 2006
- Population
- Italian adults with calcium oxalate kidney stones up to 25 mm treated with shock-wave lithotripsy
- Form
- Uriston (P. niruri extract)
- Dose
- 2 g/day
- Duration
- At least 3 months (follow-up 180 days)
- Source
- Reference 11 · PubMed 16890682 (opens PubMed)
CGrade CLiver enzymes and fibrosis score with a P. niruri and milk thistle combinationLiverNo difference from placeboRCT
n 128 · 2025
No effect ALT fell within both dose groups, but the percentage change in ALT and AST and the Fib-4 score did not differ from placebo. The capsules were well tolerated.
- Design
- RCT, n = 128, 2025
- Population
- Egyptian adults with risk factors for non-alcoholic steatohepatitis (146 enrolled)
- Form
- Heptex capsules: 200 mg P. niruri extract plus 100 mg milk thistle extract
- Dose
- 1 or 2 capsules a day (200–400 mg P. niruri)
- Duration
- 36 weeks
- Source
- Reference 12 · PubMed 39789561 (opens PubMed)
CGrade CLiver function in alcoholic hepatitisLiverLiver tests unchangedRCT
n 71 · 2021
Mixed Liver and kidney function tests did not improve versus placebo. Total antioxidant levels rose (P = 0.034) and appetite improved (P = 0.03).
- Design
- RCT, n = 71, 2021
- Population
- Indian adults with mild-to-moderate alcoholic hepatitis
- Form
- P. niruri
- Dose
- Not stated in the abstract
- Duration
- 4 weeks
- Source
- Reference 4 · PubMed 34975132 (opens PubMed)
CGrade CUrine chemistry and stone passage in calcium stone formersKidney stonesSubgroup effect onlyRCT
n 69 · 2004
Mixed No overall change in urinary calcium, uric acid, citrate, oxalate or other measures and no difference in stone passage or pain versus placebo; in the subgroup with high urinary calcium, urinary calcium fell.
- Design
- RCT, n = 69, 2004
- Population
- Brazilian adults who form calcium kidney stones
- Form
- P. niruri capsules
- Dose
- 450 mg capsules (frequency abbreviated 'td' in the abstract)
- Duration
- 3 months
- Source
- Reference 1 · PubMed 15221244 (opens PubMed)
DGrade DUrine chemistry and stone eliminationKidney stonesLower oxalate in high-oxalate subgroupOpen-label trial
n 56 · 2018
Improved Urinary potassium rose; in people with high urinary oxalate, oxalate fell from 59.0 to 28.8 mg/24 h, and in those with high uric acid, uric acid fell. Serum measures were unchanged, and the authors report stone elimination.
- Design
- Open-label trial, n = 56, 2018
- Population
- Brazilian adults with kidney stones under 10 mm
- Form
- P. niruri infusion (tea)
- Dose
- Not stated in the abstract
- Duration
- 12 weeks
- Source
- Reference 7 · PubMed 29617079 (opens PubMed)
DGrade DHepatitis B viral loadHepatitis BNo effect on viral loadRCT
n 47 · 2018
No effect No difference in viral load versus placebo and no HBsAg clearance; kidney function was unchanged and no serious adverse events occurred. The trial was stopped early for lack of benefit.
- Design
- RCT, n = 47, 2018
- Population
- Adults with chronic hepatitis B
- Form
- P. niruri
- Dose
- Not stated in the abstract
- Duration
- 12 months
- Source
- Reference 2 · PubMed 30372693 (opens PubMed)
What the numbers add up to
Each point is worked out from the data and the sources numbered on this page, with the arithmetic shown under it. It adds no new data and is not medical advice.
Studied doses
Doses used in research, shown against the official limits. They describe the studies, not a recommendation for you.
Studied doses in research, not advice. These are amounts used in research, not personal advice. Your clinician or pharmacist can say what fits you.
Doses studied in human trials
Doses studied in human trials ranged from 200–400 mg/day of P. niruri extract in a combination capsule with milk thistle for 36 weeks, through 450 mg capsules (daily frequency abbreviated 'td' in the abstract) for 3 months in stone formers and 2 g/day for at least 3 months after lithotripsy, to 3,000 mg/day of a standardized extract for 12 months in fatty liver. These are research doses, not recommendations.121113
Interactions and safety
Published interactions only: each row cites a source. No row means none was found in our sources, not that a combination is safe.
Interactions
0 agentsNone found in our sources.
Check with what you take
Kept on this device onlyAdd what you take. We list every interaction our evidence profiles cite between Chanca piedra and your picks, and between your picks.
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Add a supplement or medicine you take to check it against Chanca piedra.
Starting from one medicine? The interaction checker rates how serious each pair is, on a curated list of 19 entries for 11 medicines. This cabinet has no severity rating: it lists every interaction row our supplement pages cite.
Who should be careful
4 groups- People who form oxalate kidney stones
- Chanca piedra supplements contained about 8.2 mg oxalate per dose in a laboratory analysis, and evidence that they reduce stones is limited; stone care is best guided by a urologist.86
- People with hepatitis B or liver disease
- Placebo-controlled trials in hepatitis B, fatty liver and alcoholic hepatitis did not improve their main outcomes, so it is no substitute for medical care.2345
- People on diabetes or blood-pressure medicines
- In a 10-day uncontrolled study of nine people with mild high blood pressure (four with diabetes), P. amarus, which the paper lists as a synonym of P. niruri, lowered blood glucose and blood pressure and increased urine output. No study has tested chanca piedra alongside diabetes, blood-pressure or diuretic medicines, so the combination could in theory push glucose or blood pressure too low; check with your prescriber and monitor more closely.10
How to read the label
What to check on the Supplement Facts panel.
How to read the label
1 checksSpecies
Products may contain P. niruri or related Phyllanthus species, and the Cochrane review asked future trials to report the species used. Results for one species may not apply to another.5
Frequently asked questions
Short answers to common questions; the numbers link to the sources below.
Common questions
7 answersDoes chanca piedra dissolve kidney stones?
Does chanca piedra help the liver?
Does chanca piedra help after lithotripsy?
In a 150-person Italian trial, 2 g a day for at least 3 months after shock-wave lithotripsy gave 93.5% vs 83.3% stone-free at 180 days, which was not significant overall; the authors report a benefit only for lower-pole stones. There was no placebo.11
Is chanca piedra safe?
How long was chanca piedra taken in studies?
Does chanca piedra interact with medications?
No interaction study has been published. In a 10-day uncontrolled study of nine people, Phyllanthus lowered blood glucose, lowered systolic blood pressure in some subgroups and increased urine output, so effects could add to diabetes, blood-pressure or diuretic medicines.10
Sources
12 sources: trial abstracts, NIH fact sheets and reference databases. Numbers in the text link here.
Sources cited on this page
12 sources- 1Phyllanthus niruri normalizes elevated urinary calcium levels in calcium stone forming (CSF) patients.RCT Urol Res, 2004 · PMID 15221244
- 2Phyllanthus niruri versus Placebo for Chronic Hepatitis B Virus Infection: A Randomized Controlled Trial.RCT Complement Med Res, 2018 · PMID 30372693
- 3Effects of one-year supplementation with Phyllanthus niruri on fibrosis score and metabolic markers in patients with non-alcoholic fatty liver disease: A randomized, double-blind, placebo-controlled trial.RCT Heliyon, 2023 · PMID 37313177
- 4Efficacy of Phyllanthus niruri on improving liver functions in patients with alcoholic hepatitis: A double-blind randomized controlled trial.RCT Indian J Pharmacol, 2021 · PMID 34975132
- 5Phyllanthus species for chronic hepatitis B virus infection.Meta-analysis Cochrane Database Syst Rev, 2011 · PMID 21491412
- 6Phyllanthus niruri (stone breaker) herbal therapy for kidney stones; a systematic review and meta-analysis of clinical efficacy, and Google Trends analysis of public interest.Meta-analysis Can J Urol, 2020 · PMID 32333735
- 7Effect of phyllanthus niruri on metabolic parameters of patients with kidney stone: a perspective for disease prevention.Open-label trial Int Braz J Urol, 2018 · PMID 29617079
- 8Evaluation of the Online Information Landscape and Oxalate Content of Purportedly Antilithogenic Ingredients.Review J Endourol, 2026 · PMID 41460700
- 9Phyllanthus niruri in the management of nephrolithiasis: A systematic review of the literature.Systematic review Actas Urol Esp (Engl Ed), 2025 · PMID 40480426
- 10Diuretic, hypotensive and hypoglycaemic effect of Phyllanthus amarus.Open-label trial Indian J Exp Biol, 1995 · PMID 8786163
- 11Can Phyllanthus niruri affect the efficacy of extracorporeal shock wave lithotripsy for renal stones? A randomized, prospective, long-term study.RCT J Urol, 2006 · PMID 16890682
- 12The activity of a herbal medicinal product of Phyllanthus niruri and Silybum marianum powdered extracts (Heptex®) in patients with apparent risk factors for nonalcoholic steatohepatitis: a phase II, multicentered, randomized, double-blind, placebo-controlled clinical trial.RCT BMC Complement Med Ther, 2025 · PMID 39789561
What changed
Every dated change to this page: what changed, who made it and why.
Change log
2 entries| Date | Change | Who and why |
|---|---|---|
| evidence; studied doses; FAQ; questions; related | Added the 2006 randomised lithotripsy trial (stone clearance, 150 people) and the 2025 phase II trial of a P. niruri and milk thistle combination in people at risk of NASH (no difference from placebo); widened studied doses accordingly. Three FAQ items, three page questions and a goal-hub link. Interaction check: LactMed and LiverTox have no Phyllanthus entry, NCCIH and MedlinePlus have no page, and a PubMed search found no human interaction study (only laboratory work), so the interactions list stays empty and the glucose and blood-pressure caution stays under Who should be careful. Pregnancy note unchanged (no human data). PubMed search for meta-analyses and RCTs to October 2026 found nothing newer for stones or hepatitis B. | Writer: Kymata Health EditorialTrigger: A–Z audit against docs/supplements/AUDIT-STANDARD.md |
| all | Initial editorial evidence review (first draft). Every PMID checked against NCBI E-utilities esummary (titles and years taken from the record, none retracted) and the abstract read for each cited row. Studied doses are reported as research doses, not dosing advice. | Writer: Kymata Health EditorialTrigger: new page |
Supplement & Nutrient Encyclopedia. Educational information only; it is not medical advice and does not replace a clinician. Dietary supplements are not intended to diagnose, treat, cure or prevent any disease. Statements about supplements have not been evaluated by the FDA.