An Evaluation of the Outcomes of Bariatric Surgery - a Cohort Study

Recruiting · NCT02811900 · Observational (researchers observe without assigning treatment) · Lead sponsor: IHU Strasbourg

View the official record on ClinicalTrials.gov →

Obesity

Interventions studied

Gastric bandingIntragastric balloonRoux en Y gastric bypassSleeve gastrectomy

What this trial is about

A prospective bariatric database was carried out in the Department of Digestive and Endocrine Surgery at the University Hospital of Strasbourg, France, starting in January 1996. All potential candidates for obesity surgery were prospectively registered in the database. Patients were informed by the bariatric surgeon of the prospective database, and of the possibility of utilizing personal data for research purpose after anonymization. A case-control study was performed, to compare the quality of life (QoL) of patients treated for internal hernia (IH group) with the QoL of patients with an uncomplicated course after Roux en Y gastric bypass (Uncomplicated RYGB group).

Who can take part

Age range

18 Years and older

Sex

All (male and female)

Healthy volunteers

No - a diagnosis or condition is required

Phase

Not specified

Study type

Observational (researchers observe without assigning treatment)

Inclusion criteria

patient \>18 years old
BMI \> 35 kg/m²

Exclusion criteria

Incapacity of giving an informed consent

Where it is running

1 location listed.

Service de Chirurgie Digestive et Endocrinienne - Strasbourg, France

Read the full protocol, contacts and eligibility on ClinicalTrials.gov →