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Recruiting NCT04040413

Database Maintenance for Bariatric Procedures

Observational Obesity, Morbid Bariatric Surgery Candidate

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: bariatric surgery.
Who it may be relevant to
Registry conditions: Obesity, Morbid, Bariatric Surgery Candidate. Basic parameters: No limits · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Israel
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Institutional Bariatric Database Registry

Overview

Bariatric surgery registry for quality control and investigational purposes.

Interventions

  • Procedure bariatric surgery
    All bariatric procedures

Primary outcome measures

  • Surgery type [Time frame: 10 years]
  • Percent total weight loss (%TWL) [Time frame: 1 year from surgery]
  • Percent total weight loss (%TWL) [Time frame: 5 years from surgery]
  • Percent total weight loss (%TWL) [Time frame: 10 years from surgery]
  • Percent BMI loss (%BMIL) [Time frame: 1 year from surgery]
  • Percent BMI loss (%BMIL) [Time frame: 5 years from surgery]
  • Percent BMI loss (%BMIL) [Time frame: 10 years from surgery]
Secondary outcome measures (5)
  • Co-morbidity resolution [Time frame: 1 year from surgery]
  • Co-morbidity resolution [Time frame: 5 years from surgery]
  • Co-morbidity resolution [Time frame: 10 years from surgery]
  • 30 day morbidity/mortality [Time frame: up to 30 days from intervention]
  • long-term morbidity/mortality [Time frame: 31 days to 10 years from surgery]

Eligibility criteria

Inclusion criteria

  • morbid obesity

Exclusion criteria

  • unfit for surgery

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

Israel · 1 center
  • Sheba Medical Center — Ramat Gan

Identifiers

NCT: NCT04040413 · SMC-14-1828

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗