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Clinical Trials in China / NCT05764629
Active, not recruiting Observational

An Observational Study on Post-chronic Pancreatitis Diabetes Mellitus

NCT05764629 · tracked via the Priya Life Science China tracker
Sponsor
Changhai Hospital
Phase
Observational
Started
2021-09-01
Last updated
2023-05-26

Condition(s) studied

Chronic PancreatitisDiabetes Mellitus

Investigational drug(s) / intervention(s)

blood testpharmacologic approaches to glycemic treatment

blood test: Testing the peripheral blood for PPDM-C, including blood glucose, glycated hemoglobin A1c, fasting insulin and C-peptide, etc.

pharmacologic approaches to glycemic treatment: documenting the change of glycemic treatment during the follow-up period

Study summary

To explore the risk factors influencing glycemic status, optimized treatment, and prognosis of post-chronic pancreatitis diabetes mellitus (PPDM-C).

Eligibility

Sex
ALL
Min age
—
Max age
—
Healthy volunteers
No
Inclusion Criteria: 1. patients with diagnosis of chronic pancreatitis and diabetes mellitus. 2. participants with painless chronic pancreatitis were diagnosed with diabetes within 2 years of the diagnosis of chronic pancreatitis. 3. participants with painful chronic pancreatitis were diagnosed with diabetes after the first attack of chronic pancreatitis. Exclusion Criteria: 1. participants with suspected malignant tumors of the pancreas or other sites of body, or participants in the terminal stage of severe disease 2. serious mental illness, lesion of liver or kidney, pregnancy, breast-feeding or planning pregnancy 3. definitely diagnosed type 1 diabetes, type 2 diabetes, or other metabolic diseases that affect blood glucose 4. autoimmune pancreatitis 5. Scarcity of information related to HbA1c 6. death or loss of follow-up during follow-up

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Shanghai Changhai Hospital Shanghai China

More Changhai Hospital trials in China

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05764629 on ClinicalTrials.gov ↗ ← All trials in China