Lap-Band Surgery on Adolescents for Safety and Efficacy



Status:Active, not recruiting
Conditions:Obesity Weight Loss
Therapuetic Areas:Endocrinology
Healthy:No
Age Range:14 - 17
Updated:10/21/2018
Start Date:June 2005
End Date:August 2019

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A Prospective, Open-label Study to Evaluate the Safety and Efficacy of Lap-Band® Adjustable Gastric Band (LAGB®) Operations in the Treatment of Morbidly Obese Adolescents (Ages 14-17)

This study is to demonstrate the safety and efficacy of the use of the LAP-BAND surgery in
the morbidly obese adolescent population.

STUDY OBJECTIVES: Is to demonstrate the safety and efficacy of the use of the LAP-BAND®
System in the morbidly obese adolescent population in the United States, and therefore
provide these individuals with a significantly less morbid and reversible surgical option for
weight loss.

STUDY VARIABLES:The primary efficacy variable is weight loss evaluated in terms of % excess
weight loss (EWL).

DESIGN:Prospective, open-label, and single center

Inclusion Criteria:

- Be at least 14 and less than 18 years of age at the time of enrollment into the study.

- Have a BMI of at least 40

- Have a history of obesity for at least 5 years, including failed attempts at diet and
medical management of obesity.

- Confirmation by a psychologist or psychiatrist experienced with adolescents that the
subject is sufficiently mature emotionally to comply with the study protocol.

Express willingness to follow protocol requirements.

•Assure investigators that subject, if female of childbearing potential, is using an
appropriate form of contraception.

Exclusion Criteria:

- Intention or need to have another surgical procedure for weight reduction within 12
months of Lap Band placement.

- History of congenital or acquired anomalies of the G.I. tract, such as; congenital or
acquired intestinal telangiectasia, Crohn's disease or ulcerative colitis; severe
cardiopulmonary disease or severe coagulopathy; hepatic insufficiency or cirrhosis.

- Presence of dysphagia or documented esophageal dysmotility.

- Patients with autoimmune connective tissue disorders

- Patients with acute abdominal infections

- Pregnancy or intention of becoming pregnant in the next 12 months.

- Presence of psychiatric problems or immaturity which would compromise cooperation with
the study protocol.

- History of previous bariatric surgery, intestinal obstruction or adhesive peritonitis.

- Presence of localized or systemic infection at the time of surgery.

- Chronic use of aspirin and/or non-steroidal anti-inflammatory medications and
unwillingness to discontinue the use of these concomitant medications.

- History of gastric or esophageal surgery.

- Use of weigh loss medications simultaneously
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