Sprayshield as Adhesion Barrier System for Obese Patients

University Hospital Center (CHU)

Status: Completed

Conditions: Severe Obesity

Treatments: Procedure: ablation of gastric

Study type: Observational

Funder types: Other

Identifiers

NCT02142660

UF8744

Details and patient eligibility

About

The application of SprayShield during a laparoscopic band removal (first surgical step) will be evaluated to see if the postoperative adhesions between the stomach, the left liver and the diaphragm are not severe, facilitating the surgical surgical step of a gastric bypass or a sleeve gastrectomy.

Full description

Monocenter and observational study on 20 obese patients, requiring removal of the gastric band for poor results (weight regain or insufficient weight-loss) or mechanical complications of the band ( slippage, esophageal dilation) and schedule for a second step surgery of gastric bypass or sleeve gastrectomy 2 months later.

Enrollment: 20 patients

Sex: All

Ages: 18 to 65 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Obese male or female who would benefit from a gastric band removal and for whom a second surgical step with conversion to sleeve gastrectomy or bypass is scheduled

Exclusion criteria

• The patients having an ablation of ring motivated for an infectious complication

Trial design

20 participants in 1 patient group

Sprayshield

Description:

Applied to the operating zone during an ablation of gastric died ring at obese patients programmed for the second bariatric surgery to type of bypass gastric or of gastrectomie

Treatment:

Procedure: ablation of gastric