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Study identifier: NCT07378137 Synced from ClinicalTrials.gov · July 29, 2026
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Comparing the Components of Composite Endpoints for Healthcare Providers and Patients

Condition: Coronary Artery Disease · Percutaneous Coronary Intervention  ·  Sponsor: Xijing Hospital

PhaseN/A
Planned participants600
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Clinical trials often employ a composite primary endpoint to increase event rates and enhance trial efficiency. However, analytic approaches to composite endpoints typically assume that the individual components are of similar importance. In practice, a treatment often has different effects on each individual endpoint, leading to uncertainty in interpreting the results of a clinical trial employing a composite primary endpoint. Some investigators have recommended using a weighted composite endpoint to address these concerns, in which individual components are valued relative to one another. However, data to inform the weighting of individual endpoints, using opinions from both medical staff and patients, remains controversial. Furthermore, prior efforts to weigh composite endpoints have assumed that patients, physicians, and clinical trialists would assign similar values to individual events. If patients value endpoints differently from trialists, this would suggest that efforts to develop weighted composite endpoints may also need to address patient preferences. In the current study, we aim to record the weighing of both patients and medical staff towards a composite endpoint frequently used in cardiovascular clinical trials. To better understand the value of each endpoint for patients and medical staff, we quantified the relative severity of each endpoint when compared to death and assessed for rating differences between the two groups. Additionally, we investigated wheth…

This description comes directly from the study's public registry record.

Talk to the study team

Ruining Zhang, BSc  ·  86-15802990370  ·  ruining-zhang@qq.com

Always discuss trial participation with your own doctor first.

Locations (1)

Xijing HospitalXi'an, Shaanxi, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT07378137