Evaluation of OGTT in Patients With Post-pancreatitis Diabetes Mellitus for Diagnosis and Characterization

Sponsor
Changhai Hospital (Other)
Overall Status
Recruiting
CT.gov ID
NCT05989867
Collaborator
(none)
200
1
24
8.3

Study Details

Study Description

Brief Summary

To evaluate the islet function and insulin secretion pattern of post-pancreatitis diabetes mellitus by oral glucose tolerance testing, and to explore the pathophysiological characteristics of PPDM-C which provide evidence for the diagnosis of PPDM-C.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: blood test
  • Device: Continuous Glucose Monitor

Detailed Description

Blood samples will be collected from patients with chronic pancreatitis by oral glucose tolerance test (steamed bun meal test, SBMT) to assess their pancreatic islet function and insulin secretion pattern, measure other intestinal hormones, exosomes, plasma metabolites, and serum biochemical factors to characterize the pathophysiological features of PPDM-C and provide evidence for the diagnosis of PPDM-C. In order to better understand the glycemic fluctuations in patients with chronic pancreatitis combined with diabetes and guide subsequent treatment, Continuous Glucose Monitoring would be used in patients with chronic pancreatitis who had new-onset diabetes or poor glycemic control.

Study Design

Study Type:
Observational
Anticipated Enrollment :
200 participants
Observational Model:
Cohort
Time Perspective:
Cross-Sectional
Official Title:
Evaluation of Oral Glucose Tolerance Testing in Patients With Post-pancreatitis Diabetes Mellitus for Diagnosis and Characterization: a Cross-sectional Trial
Actual Study Start Date :
Mar 1, 2023
Anticipated Primary Completion Date :
Dec 1, 2024
Anticipated Study Completion Date :
Mar 1, 2025

Arms and Interventions

Arm Intervention/Treatment
CP

patients with chronic pancreatitis but not combined with diabetes

Diagnostic Test: blood test
Evaluation of islets function and insulin secretion pattern: Evaluating the venous plasma glucose, c-peptide, and insulin concentrations at 0h, 0.5h, 1h, 2h, and 3h after the SBMT in patients with chronic pancreatitis. Characterization of pathophysiological features: Measuring intestinal hormones, exosomes, serum metabolites, and serum biochemical factors

PPDM-C

patients with post-chronic pancreatitis diabetes mellitus

Diagnostic Test: blood test
Evaluation of islets function and insulin secretion pattern: Evaluating the venous plasma glucose, c-peptide, and insulin concentrations at 0h, 0.5h, 1h, 2h, and 3h after the SBMT in patients with chronic pancreatitis. Characterization of pathophysiological features: Measuring intestinal hormones, exosomes, serum metabolites, and serum biochemical factors

Device: Continuous Glucose Monitor
blood glucose will be monitored 24 hours a day from 7 to 14 days by wearing continuous glucose monitor(only for patients who had new-onset diabetes or poor glycemic control )

CP+IGT

patients with chronic pancreatitis combined with impaired glucose tolerance

Diagnostic Test: blood test
Evaluation of islets function and insulin secretion pattern: Evaluating the venous plasma glucose, c-peptide, and insulin concentrations at 0h, 0.5h, 1h, 2h, and 3h after the SBMT in patients with chronic pancreatitis. Characterization of pathophysiological features: Measuring intestinal hormones, exosomes, serum metabolites, and serum biochemical factors

Device: Continuous Glucose Monitor
blood glucose will be monitored 24 hours a day from 7 to 14 days by wearing continuous glucose monitor(only for patients who had new-onset diabetes or poor glycemic control )

CP+T2DM

patients with chronic pancreatitis combined with type 2 diabetes mellitus

Diagnostic Test: blood test
Evaluation of islets function and insulin secretion pattern: Evaluating the venous plasma glucose, c-peptide, and insulin concentrations at 0h, 0.5h, 1h, 2h, and 3h after the SBMT in patients with chronic pancreatitis. Characterization of pathophysiological features: Measuring intestinal hormones, exosomes, serum metabolites, and serum biochemical factors

Device: Continuous Glucose Monitor
blood glucose will be monitored 24 hours a day from 7 to 14 days by wearing continuous glucose monitor(only for patients who had new-onset diabetes or poor glycemic control )

Outcome Measures

Primary Outcome Measures

  1. steamed bun meal test result 1 [Within 5 hours after the end of the steamed bread meal test]

    Levels of glucose under the steamed bun meal experiment (100g flour made steamed bun)

  2. steamed bun meal test result 2 [Within 6 hours after the end of the steamed bread meal test]

    Levels of c-peptide bun meal experiment (100g flour made steamed bun)

  3. steamed bun meal test result 3 [Within 7 hours after the end of the steamed bread meal test]

    Levels of insulin under the steamed bun meal experiment (100g flour made steamed bun)

Secondary Outcome Measures

  1. gut hormone [up to 1 month]

    Levels of gut hormone under the steamed bun meal experiment (100g flour made steamed bun)

  2. Continuous glucose monitor results [after using continuous glucose monitor device for 7-14 days]

    Time to target range (TIR) : the proportion of time with blood glucose fluctuation

  3. glycemic control [at the time of enrollment]

    glycosylated hemoglobin(%)

Eligibility Criteria

Criteria

Ages Eligible for Study:
15 Years to 85 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. Age 15-85

  2. patients with the diagnosis of chronic pancreatitis and diabetes mellitus (exclude type 1 diabetes).

  3. participants with painless chronic pancreatitis were diagnosed with diabetes within 2 years of the diagnosis of chronic pancreatitis.

  4. participants with painful chronic pancreatitis were diagnosed with diabetes after the first attack of chronic pancreatitis.

  5. patients with chronic pancreatitis were previously diagnosed type 2 diabetes mellitus for more than 3 years.

Exclusion Criteria:
  1. Participants with suspected malignant tumors of the pancreas or other sites of the body (including pancreatic cyst and Benign pancreatic tumor), or participants in the terminal stage of severe disease

  2. Prior pancreatic surgery (including total pancreatectomy, pancreaticoduodenectomy, distal pancreatectomy, pancreatojejunostomy, or Frey), and prior bariatric or gastrointestinal surgery.

  3. Serious mental illness, lesion of the liver (alanine aminotransferase or aspartate aminotransferase > 3 times the upper reference limit) or kidney (eGFR<60 mL/min/1.73 m2), pregnancy, breastfeeding or planning pregnancy, or accompanied with active liver diseases such as hepatitis B or hepatic cirrhosis.

  4. Diagnosed type 1 diabetes, or other metabolic diseases that affect blood glucose

  5. Using high-dose insulin preparations, or drugs affecting glucose metabolism (oral steroids, thiazide diuretics, beta-blockers, beta-agonist, nicotinic acid, immunosuppressant agents, antiretroviral drugs, and antipsychotics)

  6. Acute complications of diabetes (diabetic ketoacidosis, severe hypoglycemia), severe microvascular disease (proliferative diabetic retinopathy, known diabetic nephropathy or neuropathy requiring treatment), and macrovascular disease (uncontrolled arterial hypertension, uncontrolled coronary artery disease, congestive heart failure, history of cerebrovascular event, seizure disorder, syncope, adrenal insufficiency, neurologic disease or atrial fibrillation) within the 12 months prior to enrollment.

  7. Hospitalization for acute pancreatitis within the 2 months prior to enrollment or currently suffering acute inflammation.

  8. Have been enrolled or currently participating in other clinical trials within the 3 months prior to enrollment.

  9. Patients who refused to participate in the study

Contacts and Locations

Locations

Site City State Country Postal Code
1 Department of Gastroenterology, Changhai Hospital Shanghai Shanghai China 200433

Sponsors and Collaborators

  • Changhai Hospital

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Zhuan Liao, professor, Changhai Hospital
ClinicalTrials.gov Identifier:
NCT05989867
Other Study ID Numbers:
  • ESTABLISH
First Posted:
Aug 14, 2023
Last Update Posted:
Aug 14, 2023
Last Verified:
Jul 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 14, 2023