NCT05894811

Brief Summary

The study will be conducted in the following population: obese patients with normal glucose tolerance (HbA1c ≤ 5.6%, n=12), pre-sugar patients (5.7% ≤ HbA1c ≤ 6.4%, n=18) and patients with T2DM (HbA1c ≥ 6.4% , n=18). After recruiting, they were followed up at 1, 3, 6, and 12 months postoperatively, and their preoperative and follow-up examination values related to demographics, body composition, blood biochemistry, and glucose metabolic balance, as well as quantitative MRI imaging and oral glucose tolerance test (OGTT) will be collected. An interim analysis will be performed at 6 months postoperatively and overall analysis will be performed at 12 months postoperatively by descriptive statistics and ANOVA methods to explore the effect of adiposity on the progression of diabetes mellitus and insulin secretory function.

Trial Health

65
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
48

participants targeted

Target at P25-P50 for all trials

Timeline
7mo left

Started Jun 2023

Typical duration for all trials

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress84%
Jun 2023Dec 2026

First Submitted

Initial submission to the registry

May 30, 2023

Completed
2 days until next milestone

Study Start

First participant enrolled

June 1, 2023

Completed
7 days until next milestone

First Posted

Study publicly available on registry

June 8, 2023

Completed
3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2026

Expected
6 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2026

Last Updated

June 8, 2023

Status Verified

May 1, 2023

Enrollment Period

3 years

First QC Date

May 30, 2023

Last Update Submit

June 7, 2023

Conditions

Keywords

Diabete Type 2Obesity

Outcome Measures

Primary Outcomes (2)

  • Visceral fat content

    Visceral fat content (MRI)

    1 day

  • Islet function indicators

    indicators describing Islet function calculated from OGTT data using MTT model

    1 day

Study Arms (3)

control

obese people with normal glucose tolerance

Diagnostic Test: oral glucose tolerance testDiagnostic Test: MRI

IGT

obese people with injured glucose tolerance

Diagnostic Test: oral glucose tolerance testDiagnostic Test: MRI

T2D

obese people with type 2 diabetes

Diagnostic Test: oral glucose tolerance testDiagnostic Test: MRI

Interventions

Nine blood samples were collected from subjects within 4 hours of oral glucose administration, 0 min before oral glucose administration, and 10, 20, 30, 60, 90, 120, 180, 240 min afterwards, and 4 mL of venous blood was collected at each time point for glucose, C-peptide and insulin concentrations.

IGTT2Dcontrol
MRIDIAGNOSTIC_TEST

Using MRI to quantify of fat content in the liver and pancreas of the subjects

IGTT2Dcontrol

Eligibility Criteria

Age16 Years - 65 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Obese people who will undergo sleeve gastrectomy in Peking University Third Hospital and meet the admission criteria.

You may qualify if:

  • BMI ≥ 28 kg/m2, meeting the indications for surgical weight loss surgery (gastrectomy)
  • Normal glucose tolerance group: HbA1c ≤ 5.6%; ≥ 6 cases aged 24 years or above
  • IGT patients: 5.7% ≤ HbA1c ≤ 6.4%; ≥ 12 cases aged 24 years or above
  • T2DM patients: Subjects with HbA1c ≥ 6.4% or HbA1c well controlled by medication can be diagnosed as T2DM based on self-reported or fasting/postprandial blood glucose diagnosis; ≥ 12 cases aged 24 years and above.
  • Between the ages of 16 and 65 (inclusive), with no less than one-third of either gender
  • The subjects understand the content of the informed consent form and voluntarily sign it, which allows them to maintain good communication with the researchers and comply with the requirements of the clinical trial

You may not qualify if:

  • Type I diabetes patients (autoimmune diabetes patients with T1DM antibody)
  • Suffering from special types of diabetes, including cortisolism, growth hormone tumor, glucagon tumor and diabetes caused by some genetic factors
  • Significant weight loss occurred before enrollment (\>3% weight loss in the first 3 months)
  • Participated in other research projects as a subject within 6 months prior to screening
  • Donate or lose ≥ 400 mL of blood within 8 weeks prior to screening
  • Regular use (cumulative use for 3 months in the past 12 months) or treatment with corticosteroids, contraceptives, thiazide diuretics, and quinolone antibiotics in the past two months
  • Regular use (cumulative use for 3 months in the past 12 months) or treatment with anti obesity drugs in the past two months
  • The following hypoglycemic drugs have been used routinely (for 3 months accumulatively in the past 12 months) or in the past two months: sulfonylureas (glibenclamide, glipizide, gliclazide, gliquidone, glimepiride, etc.), non sulfonylureas (repaglinide, nateglinide, migglinide, etc.), GLP-1 receptor agonists (exenatide, lilalutide, etc.) DPP-4 inhibitors (sigliptin, alogliptin, vildagliptin, shagliptin, linagliptin, etc.) or glucokinase agonists (doegliptin, etc.)
  • Contraindications to magnetic resonance imaging
  • The risk of complications significantly increases during the perioperative or postoperative period
  • Those with a history of other weight loss surgeries
  • Individuals with a history of cardiovascular surgery and severe cardiovascular and pulmonary diseases: including stroke, severe coronary heart disease, arrhythmia, unstable angina, myocardial infarction within 6 months, peripheral vascular disease, heart failure, and uncontrolled hypertension
  • Clinically significant history of ECG abnormalities or family history of long QT syndrome (grandparents, parents, brothers and sisters)
  • People with a history of kidney disease: have a history or evidence of renal insufficiency, manifested as clinically significant creatinine abnormalities or urinary composition abnormalities (such as tubular abnormalities), or eGFR\<60 ml/min/1.73m2
  • Patients with a history of gastrointestinal surgery (excluding appendectomy and cholecystectomy), inflammatory bowel disease, esophageal disease, including severe refractory esophagitis, Barrett's disease, esophageal motility disorders, or other gastric motility impairments, or those with esophageal hiatal hernia\>3cm in size, chronic or acute bleeding, including peptic ulcer disease, portal hypertension (gastric or esophageal varices), chronic pancreatitis or cirrhosis
  • +9 more criteria

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Biospecimen

Retention: SAMPLES WITH DNA

whole blood

MeSH Terms

Conditions

Diabetes Mellitus, Type 2Obesity

Interventions

Glucose Tolerance Test

Condition Hierarchy (Ancestors)

Diabetes MellitusGlucose Metabolism DisordersMetabolic DiseasesNutritional and Metabolic DiseasesEndocrine System DiseasesOverweightOvernutritionNutrition DisordersBody WeightSigns and SymptomsPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

Blood Chemical AnalysisClinical Chemistry TestsClinical Laboratory TechniquesDiagnostic Techniques and ProceduresDiagnosisDiagnostic Techniques, EndocrineInvestigative Techniques

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
researcher

Study Record Dates

First Submitted

May 30, 2023

First Posted

June 8, 2023

Study Start

June 1, 2023

Primary Completion (Estimated)

June 1, 2026

Study Completion (Estimated)

December 1, 2026

Last Updated

June 8, 2023

Record last verified: 2023-05

Data Sharing

IPD Sharing
Will not share