Naltrexone/Bupropion With or Without Very Low Calorie Ketogenic Diet for Weight Regain After Bariatric Surgery

Overview

The goal of this clinical trial is to evaluate the superiority of combined VLCKD, intensive lifestyle intervention and naltrexone/bupropion (N/B) versus standard of care with naltrexone/bupropion on weight loss for people with weight regain after bariatric surgery. The main questions it aims to answer are: Primary endpoint: • The percentage of weight loss at 26 weeks Secondary endpoints: * A weight loss percentage at 10 weeks, 16 weeks and at end of trial (= 52 weeks from start) * A proportion of patients with a weight loss percentage of 5% or more at 10, 16, 26 and 52 weeks * A proportion of patients with a weight loss percentage of 10% or more at 10, 16, 26 and 52 weeks * The time to reach a weight loss percentage of 5% and 10% * The dose of naltrexone/bupropion used at 10, 16, 26 and 52 weeks and at the end of the trial * The tolerability of VLCKD and NB * The adherence to VLCKD and NB * The Patient-Reported Outcome Measures (PROMs) of hunger and cravings at 0, 4, 10, 16, 26 and 52 weeks * The change in fasting glucose, lipids and blood pressure at 10, 16, 26 and 52 weeks Researchers will compare an experimental arm (N/B + Lifestyle + VLCKD) with comparator arm (NB + lifestyle) to see if combined VLCKD, intensive lifestyle and N/B is superior. Participants will: * get NB and lifestyle changes for 26 weeks * follow a VLCKD in the first 10 weeks on top of it, if they belong to the experimental arm * follow NB combined with lifestyle the remaining 16 weeks * be followed-up for an extension of 26 weeks * come to the hospital at week 1, 10, 16, 26, 52

Interventions

• Other Very Low Calorie Diet
  This is a parallel multicentric longitudinal randomized controlled trial in which prospective data will be collected from the electronic health record. The inclusion and exclusion criteria will be checked and afterwards patients will be randomized to (unblinded) medication only or combination with VLCKD. Both arms include NB and lifestyle changes for 26 weeks but the patients belonging to the experimental arm must follow a VLCKD in the first 10 weeks on top of it. Like the other arm, the remaini

Primary outcome measures

• To evaluate the superiority of combined VLCKD, intensive lifestyle intervention and naltrexone/bupropion versus standard of care with naltrexone/bupropion on weight loss. [Time frame: 26 weeks]

Secondary outcome measures (12)

• • A weight loss percentage at 10 weeks, 16 weeks and at end of trial (= 52 weeks from start) [Time frame: 10,16 and 52 weeks]
• • A proportion of patients with a weight loss percentage of 5% or more at 10, 16, 26 and 52 weeks [Time frame: 10, 16, 26 and 52 weeks]
• • A proportion of patients with a weight loss percentage of 10% or more at 10, 16, 26 and 52 weeks [Time frame: 10, 16, 26 and 52 weeks]
• • The time to reach a weight loss percentage of 5% and 10% [Time frame: 52 weeks]
• • The dose of naltrexone/bupropion used at 10, 16, 26 and 52 weeks and at the end of the trial [Time frame: 10, 16, 26 and 52 weeks]
• • The tolerability of VLCKD [Time frame: 52 weeks]
• • The tolerability of NB [Time frame: 52 weeks]
• • The adherence to VLCKD [Time frame: 52 weeks]
• • The adherence to NB [Time frame: 52 weeks]
• • The change in fasting glucose at 10, 16, 26 and 52 weeks [Time frame: at 10, 16, 26 and 52 weeks]
• • The change in lipids at 10, 16, 26 and 52 [Time frame: at 10, 16, 26 and 52 weeks]
• • The change in blood pressure at 10, 16, 26 and 52 [Time frame: at 10, 16, 26 and 52 weeks]

Eligibility criteria

Inclusion criteria

• Participants eligible for inclusion in this Trial must meet all of the following criteria:

• Voluntary written informed consent of the participant or their legally authorized representative has been obtained prior to any screening procedures
• Use of highly effective methods of birth control; defined as those that, alone or in combination, result in low failure rate (i.e., less than 1% per year) when used consistently and correctly; such as implants, injectables, combined oral contraceptives, some IUDs, true sexual abstinence (i.e. refraining from heterosexual intercourse during the entire period of risk associated with the Trial treatment(s)) or commitment to a vasectomised partner.
• Miminum 18 years of age at the time of Informed Consent signature
• Underwent bariatric surgery (RYGB or SG) with weight regain ≥10% of nadir weight
• People without Type 2 diabetes (T2D) • No history, no drugs, HbA1c < 6,5% and FPG <126 mg/dl) All participants that are considered for Trial participation, per the above criteria will be documented on the Screening Log, including Screen Failures.

Exclusion criteria

• Participants eligible for this Trial must not meet any of the following criteria:

• Participant has a history of type 2 diabetes mellitus (also drugs, HbA1c > 6,5% and FPG >126 mg/dl)
• IFemale who is pregnant, breast-feeding or intends to become pregnant or is of child-bearing potential and not using an adequate, highly effective contraceptive
• Participation in an interventional Trial with an investigational medicinal product (IMP) or device
• Not willing to sign informed consent
• Younger than 18 years of age at the time of Informed Consent signature
• Other types of bariatric surgery other than RYGB or SG (including LAGB, BPD)
• Underwent bariatric surgery (RYGB or SG) with weight regain <10% of nadir weight
• Contraindication for VLCKD, including CKD stage 4-5, liver cirrhosis, type 1 diabetes mellitus, active gout
• Contraindication for NB including the use of opioids, history of CNS tumor or seizures, severe psychiatric disorder or > 2 psychotropic medications, uncontrolled hypertension
• Use of other drugs for weight management (e.g. GLP1Ra) in the last 3 months prior to trial intervention
• Any disorder, which in the Investigator's opinion might jeopardise the participant's safety or compliance with the protocol Participants who meet one or more of the above exclusion criteria must not proceed to be enrolled/randomized in the Trial and will be identified on the Screening Log as Screen Failure.

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

Healthy volunteers: No

Study design

Allocation

Randomized

Model

Parallel assignment

Masking

Open label

Primary purpose

Other

Study locations

Belgium · 2 centers

• UZ Leuven — Leuven
• AZ Sint-Jan Brugge — Bruges

Identifiers

NCT: NCT06881485 · S68952

Primary sources (government registries)

• ClinicalTrials.gov (US NIH)

View this study on ClinicalTrials.gov ↗