A Behavioral Intervention to Decrease Vomiting and Improve Weight Loss in Post-Operative Laparoscopic Adjustable Gastric Banding (LAGB) Patients

Paused · Phase 2/Phase 3

Conditions studied: Bariatric Surgery Complications

In brief

The purpose of this study is to reduce problematic vomiting and associated gastrointestinal symptoms in post-operative LAGB patients. We hypothesize that our behavioral intervention will yield greater reductions in vomiting and associated symptoms compared to our control condition.

Key facts

Study ID

NCT01860053

Run by

The Miriam Hospital

People needed

5

Starts

2009-05-01

Last updated by the study team

2013-05-22

Who can join

Age: 18 and older, up to 70. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Age between 18 and 70 years.
• Received LAGB surgery with either a standard Lap-Band or a standard Realize Band.
• Report vomiting at least 3x/week.
• Agree to allow researchers to communicate with their surgeon regarding their care.
• Fulfilled all hospital surgery criteria.

You may not qualify if…

• Report a condition that in the judgment of the Principal Investigator would render them potentially unlikely to follow the protocol (e.g., major illness, plans to move out of the area, substance abuse or other significant psychiatric problems, organic brain disease).
• Report planning to become pregnant during the time frame of the investigation.
• Report a history of upper gastrointestinal dismotility.

Where it is running

• Weight Control and Diabetes Research Center — Providence, Rhode Island, United States

Full record on ClinicalTrials.gov

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