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NCT03784508: PREDI-BAR

Identification of Biomarkers of Response After Bariatric Surgery in Morbidly Obese Patients

Status unknown Last updated 10 February 2021
What this trial tests

trial in Morbid Obesity in 200 participants. Status unknown.

Timeline
1 April 2018
Primary endpoint
31 December 2021
1 April 2022

Quick facts

Lead sponsorHospital Universitari Vall d'Hebron Research Institute
StatusStatus unknown
Study typeOBSERVATIONAL
Enrollment200
Start date1 April 2018
Primary completion31 December 2021
Estimated completion1 April 2022
Sites1 location across Spain

Conditions studied

Sponsor

Hospital Universitari Vall d'Hebron Research Institute

Who can join

Adults 18 to 65, any sex, with Morbid Obesity. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The prevalence of obesity in Spain is about 21.6%. The discouraging results provided by dietary treatment, together with the lack of funding for pharmacological treatment, have led to the progressive use of bariatric surgery (CB). Besides weight loss, CB associates a beneficial effect on metabolic comorbidities. However, 25-30% of operated patients present a weight response considered inappropriate, they do not resolve their comorbidities and/or present a weight-regain shortly after surgery. Therefore, predictive strategies are necessary to allow a correct selection of obese patients who are candidates for CB. The main hypothesis of the study is that various factors such as psychopathological profile, body composition and metabolic alterations related to morbid obesity can influence the response to bariatric surgery.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Morbid Obesity

Currently open trials in the same condition.

Other Hospital Universitari Vall d'Hebron Research Institute trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03784508.

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