✓ Translated by DotMD AI Clinical Council Source: Contemporary clinical trials • Randomized Controlled Trial
Verify Primary Source: NIH PubMed PMID #17389151 ↗

Randomized Controlled Trial: Design, statistical analysis and sample size calculation of dose response study of telmisartan and hydrochlorothiazide

Original Paper Title: “Design, statistical analysis and sample size calculation of dose response study of telmisartan and hydrochlorothiazide”

Elena Rostova (AI Quant) Rigor Score
82 / 100
Sample Size (Participants)
Systematic Review
Evidence Classification
Randomized Controlled Trial
Sarah Jenkins, RN (AI Plain-English Editor) • Key Takeaways
  • The 3 by 3 factorial design was applied for this purpose and the approach for calculating sample size was proposed. This study was registered with ClinicalTrial.gov (NCT00153049).
  • Study Design & Sample: Randomized Controlled Trial published in Contemporary clinical trials (Multi-cohort synthesis).
  • Biostatistical Rigor Score: 82/100 audited by Elena Rostova (AI Biostatistician & openFDA Quant).

What the Study Found (In Plain English)

Published in Contemporary clinical trials (2007), this randomized controlled trial evaluating human clinical outcomes investigated: Many patients with hypertension take some antihypertensive drugs with complementary mechanisms of action to lower their blood pressure and achieve the therapeutic goals reducing the risk of cardiovascular events. Key clinical takeaway: The 3 by 3 factorial design was applied for this purpose and the approach for calculating sample size was proposed. This study was registered with ClinicalTrial.gov (NCT00153049).

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

Primary Endpoint & Quantitative Summary (Contemporary clinical trials, 2007-09-15; Randomized Controlled Trial; Rigor 82/100): The 3 by 3 factorial design was applied for this purpose and the approach for calculating sample size was proposed. This study was registered with ClinicalTrial.gov (NCT00153049).

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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