N/A
Completed N=517
Swedish Adjustable Gastric Banding Observational Cohort Study
Obesity, Morbid
Source: ClinicalTrials.gov NCT01183975 ↗
Enrolled (actual)
517
Serious AEs
23.8%
Results posted
Aug 2014
Primary outcomePrimary: Mean BMI Change — -9.03 kg/m^2
Summary
Longitudinal prospective cohort study of patients treated consecutively by SAGB in a sample of centers representative of this activity in France.
Verification by means of a screening log (exhaustive list of all bariatric procedures performed by participating surgeons between the beginning and end of the cohort inclusion period) requested from all centers.
No comparator group. No randomization or blinding techniques
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Mean BMI Change |
-9.03 | — |
| PRIMARY Mean Excess Weight Change |
-45.76 | — |
Eligibility Criteria
Inclusion Criteria
- morbidly obese patients (BMI>35 with comorbidities or BMI>40 without comorbidities) in France selected for gastric banding based on standard local clinical practice
Exclusion Criteria
- lower BMI, contraindications based on local clinical assessment
Data sourced from ClinicalTrials.gov (NCT01183975). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.