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NCT03623204: OBES-DYSP

Evolution of Dyspnea After Bariatric Surgery in Patient With Obesity

Completed Last updated 9 August 2018
What this trial tests

trial testing Dyspnea evaluation in Obesity in 57 participants. Completed in 1 February 2016.

Timeline
1 September 2013
Primary endpoint
1 October 2015
1 February 2016

Quick facts

Lead sponsorCHU de Reims
StatusCompleted
Study typeOBSERVATIONAL
Enrollment57
Start date1 September 2013
Primary completion1 October 2015
Estimated completion1 February 2016
Sites1 location across France

Drugs / interventions tested

Conditions studied

Sponsor

CHU de Reims — full company profile →

Who can join

18 and older, any sex, with Obesity. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Obesity, defined as a Body Mass Index greater than or equal to 30 kg/m2, represents a significant public health issue. Dyspnea is a very common and crippling symptom in obesity. About 80% of people with obesity experience dyspnea in daily living. Bariatric surgery has been demonstrated to be an excellent treatment for obesity by inducing significant weight loss. Nevertheless, changes in dyspnea in daily living after bariatric surgery and the links between variations in dyspnea and lung function tests after bariatric surgery have not been previously investigated.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Obesity

Currently open trials in the same condition.

Other CHU de Reims 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/NCT03623204.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing