[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100232937":3},{"organization":4,"armGroups":7,"interventions":13,"overallOfficials":18,"centralContacts":19,"locations":26,"responsibleParty":41,"collaborators":18,"id":43,"slug":18,"hasResults":44,"nctId":45,"briefTitle":46,"officialTitle":46,"acronym":47,"eligibilityCriteria":48,"healthyVolunteers":44,"sex":49,"minAge":50,"maxAge":18,"enrollmentInfo":51,"targetDuration":18,"studyType":54,"phases":55,"briefSummary":57,"conditions":58,"keywords":61,"overallStatus":29,"whyStopped":18,"lastUpdateSubmitDate":71,"lastUpdatePostDateStruct":72,"startDateStruct":75,"completionDateStruct":77,"leadSponsor":79,"locationsCount":80},{"fullName":5,"class":6},"University Hospital, Montpellier","OTHER",[8],{"label":9,"type":6,"description":10,"interventionNames":11},"Group\u002FCohort","all of the current bariatric surgeries are allowed in this prospective cohort study",[12],"Procedure: Bariatric surgery",[14],{"type":15,"name":16,"description":10,"armGroupLabels":17,"otherNames":18},"PROCEDURE","Bariatric surgery",[9],null,[20],{"name":21,"role":22,"phone":23,"phoneExt":24,"email":25},"David NOCCA, PUPH","CONTACT","0467337731","+33","d-nocca@chu-montpellier.fr",[27],{"facility":28,"status":29,"city":30,"state":18,"zip":31,"country":32,"cosmosGeoPoint":33,"geoPoint":38,"contacts":39},"CHRU - Hôpital Saint Eloi","RECRUITING","Montpellier","34295","France",{"type":34,"coordinates":35},"Point",[36,37],3.87635,43.61093,{"lat":37,"lon":36},[40],{"name":21,"role":22,"phone":23,"phoneExt":24,"email":25},{"type":42,"investigatorFullName":18,"investigatorTitle":18,"investigatorAffiliation":18,"oldNameTitle":18,"oldOrganization":18},"SPONSOR","100232937",false,"NCT02310178","Obesity Cohort : Medical Follow-up of Severe or Morbid Obese Patients Undergoing Bariatric Surgery","BAREVAL","Inclusion Criteria:\n\n* Only be considered in patients operated and followed at CHU Montpellier with bariatric surgery\n* Patients treated by bariatric surgery on CHU Montpellier\n* Agreed to participate to the study by signing an informed consent\n* Eligible to health insurance\n\nExclusion Criteria:\n\n* Unable to follow the patient in the long term (foreign patients, surgical use ...)\n* Inability to follow in the long run","ALL","15 Years",{"count":52,"type":53},750,"ESTIMATED","INTERVENTIONAL",[56],"NA","The aim of this cohort is to evaluate the follow-up of morbidly obese patients treated by several types of bariatric procedures. In addition, this study could lead to the development of clinical trials on assessment of the bariatric surgery impact.",[59,60],"Obesity, Morbid","Bariatric Surgery Candidate",[62,63,64,65,66,67,68,69,70],"weight loss","sleeve gastrectomy","gastric bypass","gastric banding","bariatric procedures","cohort","morbid obesity","medical and economical impact","severe obesity","2026-06-17",{"date":73,"type":74},"2026-06-22","ACTUAL",{"date":76,"type":74},"2012-05-21",{"date":78,"type":53},"2028-12",{"name":5,"class":6},1]