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NCT07378137Recruiting

Comparing the Components of Composite Endpoints for Healthcare Providers and Patients

A Preference Study Comparing the Components of Composite Endpoints for Healthcare Providers and Patients With CAD

Source: ClinicalTrials.gov · Last updated 30 Jan 2026

Brief summary (registry, in English)

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 whether endpoint weights varied by the demographic and clinical characteristics of patients and medical staff.

Status (registry)
Recruiting
Study type
Observational
Enrollment
600 (estimated)
First submitted
22 Jan 2026
Start date
18 Aug 2025
Primary completion date
1 Mar 2026
Lead sponsor
Xijing Hospital
NCT number
NCT07378137

What you commit to

  • Study type: Observational
  • Planned participants: 600
  • From 18 Aug 2025 to the primary completion date, 1 Mar 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Inability to understand the questionnaire or presence of cognitive impairment.

Age

  • Aged \< 18 years;

Who the study is looking for

  • Patients with acute or chronic coronary syndrome who have undergone percutaneous coronary intervention;
  • Patients who can understand the purpose of this trial and are willing to participate in the preference questionnaire.
  • Healthcare providers who treat patients with coronary artery disease.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Xijing hospital
Coordinator of this site? Confirm its status
Xi'anChinaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.