WR: Laparoscopic Revision Gastric Bypass for Weight Recidivism

Sponsor
University of California, San Francisco (Other)
Overall Status
Completed
CT.gov ID
NCT01040572
Collaborator
(none)
132
1
2
65.9

Study Details

Study Description

Brief Summary

The main aim of this study is to analyze and report traditional, patient-centered, and composite intermediate-term outcomes after laparoscopic revision Roux-en-Y gastric bypass surgery for weight recidivism.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    There is lack of standardization of primary and revisional bariatric surgery compounded by a scant long-term outcome data. The treatment of inadequate weight loss, weight recidivism, and most severe technical complications after primary bariatric surgery remains refractory to non-operative treatment. Failure rates have been reported up to 20% and 35% for the morbidly obese (MO) and super obese (SO), respectively at 2 to 3 years after surgery. The indication for further surgical intervention remains controversial, as does what type of revisional procedure, both operative and endoscopic, to recommend. Furthermore, there is no standardization of the limb lengths, pouch size or the use of prosthetic reinforcement. Therefore the approach to these patients must be as individualized as their original operations. We formally analyze our experience with all laparoscopic revisional strategies for weigh regain after failed gastric bypass.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    132 participants
    Observational Model:
    Cohort
    Time Perspective:
    Retrospective
    Official Title:
    Laparoscopic Revision Gastric Bypass Surgery for Weight Recidivism: Our Experience in 170 Patients
    Study Start Date :
    Oct 1, 2009
    Actual Primary Completion Date :
    Dec 1, 2009
    Actual Study Completion Date :
    Dec 1, 2009

    Arms and Interventions

    Arm Intervention/Treatment
    Obesity recidivism after gastric bypass

    Outcome Measures

    Primary Outcome Measures

    1. Weight loss expressed as Body Mass Index and Percentage Excess Weight Loss [At the lowest weight loss point and at last follow-up]

    2. Comorbidity status [throughout follow-up]

    3. Subjective Satisfaction [at last follow-up]

    4. Health-Related Quality of Life (HR-QoL). [at the last follow-up]

    5. Morbidity and mortality [throughout follow-up]

    Secondary Outcome Measures

    1. To assess failures [at yearly intervals throughout follow-up]

    2. To evaluate the patients´ metabolic and nutritional status [throughout follow-up]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 65 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • patients that underwent laparoscopic revisional "RYGB" for failed "RYGB" with weight recidivism or weight regain "WR" pattern
    Exclusion Criteria:
    • failed RYGB with an Inadequate Initial Weight Loss "IIWL" pattern

    • patients with prior major bariatric conversion or esophago-gastric surgeries

    • RYGB patients revised by an open surgical approach

    • RYGB patients who underwent laparoscopic revisional RYGB surgery somewhere else and continue their follow-up care with our program

    • missing records and/or unreachable patients with scant information for analysis

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 UCSF Fresno Center for Medical Education and Research Fresno California United States 93701

    Sponsors and Collaborators

    • University of California, San Francisco

    Investigators

    • Study Director: Francisco M Tercero, MD, Research Associate, University of California San Francisco
    • Principal Investigator: Kelvin D Higa, MD, Professor of Surgery, University of California San Francisco

    Study Documents (Full-Text)

    None provided.

    More Information

    Additional Information:

    Publications

    Responsible Party:
    , ,
    ClinicalTrials.gov Identifier:
    NCT01040572
    Other Study ID Numbers:
    • CMC IRB No. 2009078
    • U1111-1113-0216
    First Posted:
    Dec 29, 2009
    Last Update Posted:
    Dec 29, 2009
    Last Verified:
    Oct 1, 2009

    Study Results

    No Results Posted as of Dec 29, 2009