Examining Patterns in the Involvement of Gastric Bypass Patients in Clinical Studies
Not yet recruiting
- Conditions
- Gastric BypassWeight Loss Surgery
- Registration Number
- NCT05715892
- Lead Sponsor
- Power Life Sciences Inc.
- Brief Summary
Clinical trial participation has historically been heavily biased toward specific demographics.
Several people will be invited to enroll in this study so that it may collect a variety of data about gastric bypass clinical trial experiences and identify barriers to participation as well as the causes of participants' failure or withdrawal.
The information collected from this study can be used to improve patient experience and outcomes for future patients and an opportunity to contribute to the advancement of medical knowledge and treatments for gastric bypass.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- NOT_YET_RECRUITING
- Sex
- All
- Target Recruitment
- 500
Inclusion Criteria
- Age 18 years and older
- Diagnosis of obesity or disorder of metabolism undergoing routine gastric bypass surgical intervention
- Capable of giving signed informed consent.
Exclusion Criteria
- ECOG score of 4
- Ineligible for gastric bypass surgery
- Pregnant women or women actively seeking to become pregnant.
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Number of patients who decide to participate in a gastric bypass clinical study 3 months Rate of gastric bypass patients who remain until trial completion 12 months
- Secondary Outcome Measures
Name Time Method