✓ Translated by DotMD AI Clinical Council Source: JAMA • Randomized Controlled Trial
Verify Primary Source: NIH PubMed PMID #11939866 ↗

Randomized Controlled Trial: Effect of Hypericum perforatum (St John's wort) in major depressive disorder (N = 340)

Original Paper Title: “Effect of Hypericum perforatum (St John's wort) in major depressive disorder: a randomized controlled trial”

Elena Rostova (AI Quant) Rigor Score
93 / 100
Sample Size (Participants)
N = 340
Evidence Classification
Randomized Controlled Trial
Sarah Jenkins, RN (AI Plain-English Editor) • Key Takeaways
  • This study fails to support the efficacy of H perforatum in moderately severe major depression. The result may be due to low assay sensitivity of the trial, but the complete absence of trends suggestive of efficacy for H perforatum is noteworthy.
  • Study Design & Sample: Randomized Controlled Trial published in JAMA (N = 340 human participants).
  • Biostatistical Rigor Score: 93/100 audited by Elena Rostova (AI Biostatistician & openFDA Quant).

What the Study Found (In Plain English)

Published in JAMA (2002), this randomized controlled trial evaluating 340 human participants investigated: To test the efficacy and safety of a well-characterized H perforatum extract (LI-160) in major depressive disorder. Key clinical takeaway: This study fails to support the efficacy of H perforatum in moderately severe major depression. The result may be due to low assay sensitivity of the trial, but the complete absence of trends suggestive of efficacy for H perforatum is noteworthy.

Dr. Lin (AI Evidence Lead): Statistical Endpoints & Numbers

Primary Endpoint & Quantitative Summary (JAMA, 2002-04-10; N = 340; Rigor 93/100): This study fails to support the efficacy of H perforatum in moderately severe major depression. The result may be due to low assay sensitivity of the trial, but the complete absence of trends suggestive of efficacy for H perforatum is noteworthy.

Study Limitations & Caveats Before You Act

Clinical trials evaluate specific inclusion/exclusion cohorts under protocol-controlled conditions (Randomized Controlled Trial). Individual response, hepatic/renal clearance, CYP450 drug interactions, and baseline comorbidities vary; verify applicability with a board-certified physician before modifying any prescription or supplement regimen.

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