CHAMGAP
APPROVEDReviewed and approved by the Chamgap Editorial Team (2026-07-11). The draft was written by AI, the existence of all 5 cited sources was verified at the original page, and the verdict passed blind grading and adversarial audit. Methodology v0.6.
Verdict No. 212 · Search date 2026-07-11 · Methodology v0.6

Hawthorn leaf and flower extract,
does it really help with Improvement in chronic-heart-failure symptoms, exercise capacity, and blood pressure?

30-Second Summary
D
Evidence Grade D · 29 · Safety caution
Past heart-failure symptom signals for hawthorn were not replicated as functional or event benefits on modern standard therapy
What the
research shows
The central claim for hawthorn leaf and flower extract—heart-failure symptoms and exercise capacity—is D. In the independent 120-participant HERB RCT added to modern standard therapy, six-minute walk distance (P=0.61), symptoms, and function were negative, and the 2,681-participant SPICE trial also found no difference in the first cardiac event at HR 0.95. Blood pressure is at the lower end of C based on small-trial signals, but the 2025 meta-analysis abstract called systolic pressure significant while reporting a 95% CI of -11.72 to +1.59, an internal contradiction. Direct failure of the central clinical claim results in an overall D.
What the
ads claim
Advertising may combine heart strengthening, blood flow and circulation, exercise capacity, and blood-pressure balance as one product effect. Research is concentrated on specific standardized leaf-and-flower extracts, and substitution for modern heart-failure therapy or reduction of cardiac events has not been confirmed.
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Useful facts when choosing a product

  • The representative heart-failure ingredient is WS 1442, a leaf-and-flower extract standardized to 17.3-20.1% oligomeric procyanidins, commonly at 900 mg/day.
  • Evidence on hawthorn berry extracts, teas, and camphor combinations cannot be directly combined with evidence on a single leaf-and-flower extract.
  • The large heart-failure trial tested addition to standard therapy and did not confirm a reduction in first cardiac events.
  • Long-term interaction data in people with cardiovascular disease and polypharmacy are limited, and more adverse events were reported in the HERB trial.
Gap Measurement · Verdict 212 · D 29
What advertising claims
What independent, higher-quality research supports
△ GAP
01

What the research actually shows

The Pittler 2008 Cochrane review reported improvements in exercise workload, dyspnea, and fatigue across 14 double-blind placebo-controlled trials, but actual sample sizes in several analyses were only 98-239 participants. The Holubarsch 2008 SPICE RCT added WS 1442 900 mg/day for 24 months to standard therapy in 2,681 patients with heart failure, but the first cardiac event was negative at HR 0.95 (95% CI 0.82-1.10, P=0.476). The Zick 2009 HERB RCT found no benefit in six-minute walk distance (P=0.61), quality of life, or functional capacity after six months in 120 participants. The Walker 2006 RCT found that 1,200 mg/day lowered diastolic pressure more in 79 patients with type 2 diabetes, but systolic pressure did not differ. The Szikora 2025 meta-analysis abstract covering six placebo-controlled trials and 428 participants described systolic pressure as significant while reporting a 95% CI of -11.72 to +1.59; because these statements conflict, the estimate was not treated as confirmed positive evidence.

02

Why this is classified as D (29)

The central clinical claim of heart-failure symptoms and exercise capacity is D because the 120-participant HERB trial on modern standard therapy was negative for six-minute walk distance at P=0.61, symptoms, and function, and the 2,681-participant SPICE trial was also negative for the first cardiac event at HR 0.95. Blood pressure is lower-C, and the systolic-pressure 95% CI of -11.72 to +1.59 in the 2025 meta-analysis abstract contradicts its significance wording, so it was not treated as confirmed positive. The central D claim determines the overall score of 29.

Counterpoint. Past symptom signals for standardized WS 1442 and possible blood-pressure changes with some hawthorn extracts remain. The overall D reflects direct failure of the central heart-failure clinical claim on modern standard therapy, while blood pressure is separately labeled C.

Rejudgment record. Reassessment (cross-validation incorporated) — The central heart-failure symptom and exercise-capacity claim was negative in 120 HERB participants for six-minute walk at P=0.61, symptoms, and function on modern standard therapy, and the first cardiac event in 2,681 SPICE participants was also negative at HR 0.95; blood pressure is separated as lower-C

Sub-claim grades by effect

This ingredient is marketed for several effects. A single overall grade blends strong and weak claims together, so each effect is graded separately here. The overall grade reflects the strongest disconfirming or core claim.

Effect (sub-claim)GradeBasis
Heart-failure symptoms and exercise capacityDIn 120 HERB participants on modern standard therapy, six-minute walk at P=0.61, symptoms, and function were negative; the first cardiac event in 2,681 SPICE participants was also negative at HR 0.95
Blood pressureCSmall RCT signals exist, but results and preparations are heterogeneous, and the systolic-pressure 95% CI of -11.72 to +1.59 in the 2025 meta-analysis abstract contradicts its significance wording

Cross-check — Codex and Claude

This verdict was drafted by Codex through literature review and source-existence checks, cross-checked through blind grading and adversarial audit, and settled by reapplying the methodology boundary rules. Cases with split grades were resolved through rejudgment.
03

Evidence Table

StudyDesignSampleFundingEndpointResultWeight
Pittler MH et al. 2008Cochrane systematic review and meta-analysis1,110Independent academic review; included trials had mixed links and manufacturer contactExercise workload, oxygen consumption, dyspnea, fatigue, and adverse eventsReported improved exercise workload and symptoms, but actual samples in several pooled analyses were only 98-239 participants.Key
Holubarsch CJF et al. 2008 (SPICE)Multicenter randomized double-blind placebo-controlled event trial2,681Supported by the manufacturer of WS 1442First cardiac event, cardiac death, and heart-failure hospitalizationThe 24-month first cardiac event was negative at HR 0.95, 95% CI 0.82-1.10, P=0.476; only an exploratory subgroup was positive.Key
Zick SM et al. 2009 (HERB CHF)Randomized double-blind placebo-controlled trial120Funded by the U.S. NIH/NCCAMSix-minute walk, quality of life, functional capacity, and LVEFNo benefit in six-minute walk distance (P=0.61), quality of life, or functional capacity; more adverse events were reported in the hawthorn group.Key
Walker AF et al. 2006Randomized placebo-controlled trial79UnknownSystolic and diastolic blood pressure and interactionsAfter 1,200 mg/day for 16 weeks, the between-group difference in diastolic pressure was P=0.035; systolic pressure was negative at P=0.329.Supportive
Szikora Z et al. 2025Meta-analysis of randomized placebo-controlled trials428Academic institutionsSystolic and diastolic blood pressureThe abstract describes systolic pressure as significant, but its 95% CI of -11.72 to +1.59 includes zero and is internally contradictory; diastolic pressure was not significant, and dose and design heterogeneity were substantial.Supportive
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Receipt — 5 References

All 5 cited sources were verified for existence at the original page (as of 2026-07-11).

Pittler MH, Guo R, Ernst E. Hawthorn extract for treating chronic heart failure. Cochrane Database Syst Rev. 2008;(1):CD005312. PMID: 18254076. DOI: 10.1002/14651858.CD005312.pub2.
checked
Holubarsch CJF, Colucci WS, Meinertz T, Gaus W, Tendera M. The efficacy and safety of Crataegus extract WS 1442 in patients with heart failure: the SPICE trial. Eur J Heart Fail. 2008;10(12):1255-1263. PMID: 19019730. DOI: 10.1016/j.ejheart.2008.10.004.
checked
Zick SM, Vautaw BM, Gillespie B, Aaronson KD. Hawthorn Extract Randomized Blinded Chronic Heart Failure (HERB CHF) trial. Eur J Heart Fail. 2009;11(10):990-999. PMID: 19789403. DOI: 10.1093/eurjhf/hfp116.
checked
Walker AF, Marakis G, Simpson E, et al. Hypotensive effects of hawthorn for patients with diabetes taking prescription drugs: a randomised controlled trial. Br J Gen Pract. 2006;56(527):437-443. PMID: 16762125.
checked
Szikora Z, Mátyus RO, Vargáné Szabó B, Csupor D, Tóth B. Hawthorn (Crataegus spp.) Clinically Significantly Reduces Blood Pressure in Hypertension: A Meta-Analysis of Randomized Placebo-Controlled Clinical Trials. Pharmaceuticals (Basel). 2025;18(7):1027. PMID: 40732315. DOI: 10.3390/ph18071027.
checked
Draft and rewrite: Codex (AI) · Verification: Codex blind grading and adversarial audit · Final adjudication: Claude
Reviewed and approved: Chamgap Editorial Team · Approval date: 2026-07-11 · Corrections: none

Cite this verdict

Hawthorn leaf and flower extract x improvement in chronic-heart-failure symptoms, exercise capacity, and blood pressure Evidence Grade D card
[Chamgap] Hawthorn leaf and flower extract x improvement in chronic-heart-failure symptoms, exercise capacity, and blood pressure — Evidence Grade D·29. 5 cited sources checked. Source: https://health-receipt.pages.dev/en/verdicts/heart/hawthorn-heart-failure-blood-pressure/ · CC BY 4.0

CC BY 4.0 — free to use with attribution; do not distort grades, numbers, or verdict meaning.

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What this document does and does not do

Chamgap is an information source. It reports what research has and has not confirmed; it does not tell readers what to take or buy. That decision belongs to readers and, when needed, medical or legal professionals. This verdict reflects literature available up to the search date and may change as new research appears. Nothing here is medical advice.