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Non-randomized Prospective Comparison Between SASI Bipartition and RYGB

Metabolic Syndrome Clinical Trial

Official title:
Long-term Outcomes of Bariatric Patients Treated With Gastric Bypass or Single-anastomosis Sleeve Ileal Bypass (SASI Bipartition)

Clinical Trial Summary

The main aim of this project is to assess the safety and efficiency of the SASI Bipartition.

Clinical Trial Description

The Roux-en-Y Gastric Bypass (RYGB) is the procedure of choice in morbid obesity with metabolic disorders in most of the reference centers. Recent data describes the SASI Bipartition as being as efficient on weight loss and co-morbidities as the RYGB, with the advantage of being less technically difficult and less morbidity. In order to draw definite conclusions regarding the procedure, larger series with longer follow-up are necessary. Patients with BMI over 40, or with BMI over 35 with comorbidities are offered SASI Bipartition with 300 cm common limb or standard RYGB. Follow up is performed through visits at 3, 12, 24, 36, 48, and 60 months after surgery. Results on weight loss, comorbidities resolution, complications, and need of supplements are registered. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04469712
Study type Observational [Patient Registry]
Source Aleris Hospital
Contact
Status Active, not recruiting
Phase
Start date August 1, 2020
Completion date August 1, 2027
View Details
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