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Sleeve Gastrectomy for Morbid-Obesity Sequelae After Transplantation

Sleeve Gastrectomy for Morbid-Obesity Sequelae After Transplantation: A Randomized Controlled Trial Comparing Sleeve Gastrectomy Following Liver Transplantation to No Surgical Intervention in Patients With Morbid Obesity

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03617744
Acronym
SG-4MOST
Enrollment
50
Registered
2018-08-06
Start date
2023-09-01
Completion date
2025-06-30
Last updated
2023-05-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Liver Transplantation, Obesity

Brief summary

Complications associated with excess weight (hypertension, coronary artery disease and diabetes) have become major causes of morbidity and mortality after liver transplantation (LT). To ensure excellent long-term outcomes with LT it is critically important to understand the best strategies to minimize obesity and its associated complications in our patients. Weight loss can be achieved through dieting and exercise, but most patients are unable to maintain the weight loss. In the general population, bariatric surgery is much more effective than medical treatment for permanent weight loss and prevention or reduction of obesity-associated complications. The purpose of this study is to determine the safety and effectiveness of performing sleeve gastrectomy (SG) procedure in the early post-LT period in obese patients. The patient population for this study will be anyone listed for liver transplantation at Toronto General Hospital (University Health Network, Toronto, ON, Canada) and meeting the current standard criteria for bariatric surgery (BMI\>40, or BMI\>35 with at least 1 obesity-related complication).This study will randomly assign eligible participants to one of two groups (1:1). Patients in group 1 will receive standard lifestyle/diet counselling while patients in group 2 will undergo SG-specific counselling prior to transplant and the SG procedure within 2 weeks of LT (if safe to do so). All participants will be followed for 12 months.

Interventions

PROCEDURESleeve gastrectomy

Open sleeve gastrectomy

Sponsors

University Health Network, Toronto
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

1:1 randomization to group a or group b

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* actively listed for liver transplantation at University Health Network * BMI at screening of a) \>40; or b) BMI \>35 and 1 obesity-related complication \[diabetes (defined as hyperglycemia requiring medication(s) for control), hypertension (defined as a persistently elevated systolic pressure greater than 140 mmHg and/or requiring medication(s) for control), hypercholesterolemia (defined as elevated lipids requiring medication for control)\] OR a diagnosis of Non Alcoholic Fatty Liver Disease (defined as the presence of a fatty liver on imaging without a secondary cause such as alcohol abuse) or Non Alcoholic Steatohepatitis * upper endoscopy showing no contraindications to a sleeve gastrectomy procedure

Exclusion criteria

* • Listed for re-transplantation, or transplantation of another organ (eg. kidney). * Previous bariatric surgery. * Contraindication to undergoing sleeve gastrectomy such as severe gastroesophageal reflux disease or Barrett's Esophagus * MELD (Model End-Stage Liver Disease) score \> 35 at the time of transplantation * Presence of any condition that in the opinion of the investigator(s) could compromise the patient's ability to comply with study procedures * Patients with a BMI \<32 at transplant or having weight loss of 20% or more (pre-transplant estimated dry body weight compared to estimated dry body weight at screening) * Presence of any other condition that, in the opinion of the investigator(s), could compromise the patient's ability to safely undergo, or benefit from, the SG procedure (eg. significant sarcopenia)

Design outcomes

Primary

MeasureTime frameDescription
morbid obesity12 months post-liver transplantrate of morbid obesity defined as BMI greater than or equal to 35

Secondary

MeasureTime frameDescription
surgical morbidity12 months post-transplantrate of surgical morbidity
change in weight12 monthsweight loss or gain as percentage of estimated dry weight at transplantation
surgical complications12 monthsrate of surgical complications
mortality12 months post-transplantpatient mortality
hypertension12 months post-transplantationpercentage of participants in each group requiring treatment of hypertension
diabetes12 months post-transplantationpercentage of participants in each group requiring medical treatment of diabetes
hyperlipidemia12 months post-transplantationpercentage of participants in each group requiring medical treatment of elevated lipids
sleep apnea12 months post-transplantationpercentage of participants in each group requiring BiPAP or CPAP for treatment of sleep apnea

Contacts

Primary ContactErin Winter, BSc
erin.winter@uhn.ca416-340-4800

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026