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Active not recruitingPhase 2, PHASE3

The Medically Reproducing Bariatric Surgery (MRB) II Study

The Medically Reproducing Bariatric Surgery (MRB) II Study: SEMAGLUTIDE Followed by OPTIFAST in Veterans With Type 2 Diabetes

Assets

GLP-1 / incretin class catch-all / Semaglutide

Listed sites

1

Recruiting sites

Enrollment

50

estimated

Study population

Obesity / overweight, Type 2 diabetes

Key I/E criteria

BMI ≥27HbA1c ≥7%

Primary endpoint

HbA1c, change

Footprint

Where this trial recruits

Site locations as reported to ClinicalTrials.gov. Site count is not enrollment count; per-site enrollment is not available from source.

Identifiers

Registered as

NCT IDNCT06363747
Org study ID123456

Timeline

Milestones

Study first posted2024-04-12actual
Study start2024-06-24actual
Last update posted2025-02-07actual
Primary completion2025-11-03estimated
Study completion2025-11-03estimated

Assets

Investigational agents

Study populations

Who this study enrolls

Obesity / overweightType 2 diabetes

Eligibility

Who can enroll

Minimum age25 Years
Maximum age75 Years
SexAll
Healthy volunteersNot accepted

Inclusion criteria

male or female
age 25-75 years
BMI >27
diagnosis of type 2 diabetes
weight stable for 1 month
hemoglobin A1C >7.0%
on stable dose of once weekly GLP-1 agonist
on oral or injectable DM2 medicines
interested in losing weight
agreeable to regular visits per study protocol
access to telephone and reliable transportation and has a VAMC provider
using a Freestyle Libre glucose monitoring device and/or glucometer device

Exclusion criteria

age >75,
A1C <7%
pregnant
breast feeding
prior history of pancreatitis
prior history of gastroparesis
history of thyroid cancer/multiple endocrine neoplasia/thyroid nodules/medullary thyroid cancer (contraindication to Liraglutide)
history of gallstones
history of hyperoxaluria or calcium oxalate nephrolithiasis
history of Roux-en-Y gastric bypass or gastric sleeve or any other bariatric procedure,
type 1 diabetes
any abnormality on the screening EKG that could subject patient to increased risk during the study
any gastrointestinal condition causing malabsorption (including but not limited to inflammatory bowel disease, celiac sprue)
unwilling or unable to complete scheduled testing
any serious and/or unstable medical, psychiatric, or other condition(s) that prevents the patient from providing informed consent or complying with the study
organ transplantation or those on immunosuppressants
chronic anticoagulation
recent myocardial infarction, unstable angina, stroke, coronary artery bypass or transient ischemia attacks in the past 6 months
chronic prednisone use
hepatitis
cirrhosis
GFR <50
deep vein thrombosis in past 6 months
active malignancy
unstable psychiatric condition including active or current suicidal ideation
enrolled in another research study related to diet and/or physical activity

Endpoints (5)

What's being measured

Protocol endpoints and posted registry outcome measures, grouped into outcome categories. Composite endpoints show their component event types. Standard codes (LOINC, SNOMED CT) are shown where available.

Coverage by outcome category

Glycemic / diabetes
2
Patient-reported / QoL
2
Weight & body composition
1

Weight & body composition

1 endpoint
Secondary/protocol endpoint

Weight lost

Time frame:baseline, week 12, week 24, week 48

Body weight, % change

percent change from baseline, improvement

Glycemic / diabetes

2 endpoints
Primary/protocol endpoint

Glycemic Control

Time frame:baseline, week 12, week 24, week 48

HbA1c, change

change from baseline, improvement

LOINC 4548-4

Secondary/protocol endpoint/low confidence

Medication Intensity

Time frame:baseline, week 12, week 24, week 48

descriptive, improvement

Patient-reported / QoL

2 endpoints
Secondary/protocol endpoint

Health Related Quality of Life

Time frame:baseline, week 12, week 24, week 48

change from baseline, improvement

Other/protocol endpoint

Symptom Item Checklist

Time frame:2 week run-in phase

descriptive

Publications (28)

Bibliography

Records linked to this trial through ClinicalTrials.gov references, PubMed NCT search, and curated study seeds. 'Canonical' marks design/result papers; others are registry references or candidates.

Registry references + supporting bibliography

Provenance

Sources

Trial identity, design, statusClinicalTrials.gov API v2
Snapshot dateJuly 1, 2026
Endpoint classificationDelfa endpoint taxonomy v2 (May 13, 2026)
Results tableno registry results posted yet

Trial facts come from public ClinicalTrials.gov records. Endpoint categories are Delfa's classification of those records, not a ClinicalTrials.gov field. All figures reflect the July 1, 2026 snapshot.