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Recruiting NCT03467581

Five-year Outcome of Laparoscopic Gastric Sleeve

— Observational Bariatric Surgeries Metabolic Surgery

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
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Bariatric Surgeries, Metabolic Surgery. Basic parameters: 18 years — 65 years · 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
Estonia
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

Five-year Outcome of Laparoscopic Gastric Sleeve, Resolution of Comorbidities and Risk for Cumulative Nutritional Deficiencies.

Overview

The aim of this study is to evaluate the long-term (5-year follow-up) results of laparoscopic gastric sleeve (LGS) in terms of weight loss and obesity related comorbidities, as well as the risk factors associated with postoperative nutritional deficiencies.

Detailed description

The consecutive patients who undergo LGS for the treatment of morbid obesity at Tartu University Hospital are followed prospectively in cohort study. The outpatient hospital follow-up visits are conducted at 3 months, 1 year and 5 years postoperatively.

Primary outcome measures

  • Five-year outcome of laparoscopic gastric sleeve [Time frame: 5-year follow-up]
Secondary outcome measures (2)
  • Five-year outcome of laparoscopic gastric sleeve [Time frame: 5-year follow-up]
  • Five-year outcome of laparoscopic gastric sleeve [Time frame: 5-year follow-up]

Eligibility criteria

Inclusion criteria

  • The criteria for bariatric surgery: BMI of >40, or >35 with certain obesity related comorbidities

Exclusion criteria

  • Patients who did not fill the inclusion criteria

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

Estonia · 1 center
  • Tartu University Hospital — Tartu

Identifiers

NCT: NCT03467581 · Sleeve5years

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗