Active — Not RecruitingNot Applicable

Non-randomized Prospective Comparison Between SASI Bipartition and RYGB

Norway280 participantsStarted 2020-08-01

Plain-language summary

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

Who can participate

Age range18 Years – 70 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: \- Morbid obesity with BMI ≥ 40 kg/m2 or BMI ≥ 35 kg/m2 associated with one or more co-morbidities (type 2 diabetes, arterial hypertension, sleep apnea, dyslipidemia, arthritis) Exclusion Criteria: * Mental diseases * Drug addiction * Alcoholic * Malignancy * Pregnancy

What they're measuring

Weight change

Timeframe: 3 to 60 months after surgery

Waist size change

Timeframe: 3 to 60 months after surgery

Medical and surgical complication

Timeframe: 3 to 60 months after surgery

Operative time

Timeframe: During surgery

Hemoglobin

Timeframe: before surgery up to 60 months after surgery

Albumin

Timeframe: before surgery up to 60 months after surgery

Ferritin

Timeframe: before surgery up to 60 months after surgery

Iron

Timeframe: before surgery up to 60 months after surgery

Parathyroid hormone (PTH)

Trial details

NCT IDNCT04469712

SponsorAleris Hospital

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2027-07-01

View on ClinicalTrials.gov More Obesity, Morbid trials