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Clinical Trials in China / NCT06590935
Active, not recruiting Observational

Endocrine and Exocrine Secretory Function Alterations After Moderately Severe and Severe Acute Pancreatitis

NCT06590935 · tracked via the Priya Life Science China tracker
Sponsor
Shanghai Changzheng Hospital
Phase
Observational
Started
2024-10-08
Last updated
2025-02-21

Condition(s) studied

Acute Pancreatitis (AP)Diabetes Mellitus

Study summary

The goal of this observational study is to learn about post-acute pancreatitis diabetes mellitus (PPDM-A). The main questions it aims to answer are:

1. Are the incident rates of glucose metabolic disorders (pre-diabetes and diabetes mellitus) after acute pancreatitis of different etiologies the same?
2. Are alterations in endocrine and exocrine secretory function in patients with acute pancreatitis associated with all-round outcomes?

All patients with acute pancreatitis have been given the standardized treatment for the condition.

Investigators will compare the incident rates of glucose metabolic disorders (pre-diabetes and diabetes mellitus) after acute pancreatitis of different etiologies in patients with moderately severe (MSAP) and severe acute pancreatitis (SAP) to explore the association between alterations in endocrine and exocrine secretory function and all-round outcomes.

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
No
Inclusion Criteria: 1. Male or female Chinese subjects; 2. Age ≥18 years at the time of signing the informed consent; 3. Patients with a complete diagnosis of MSAP and SAP (according to the Chinese guidelines for the diagnosis and treatment of acute pancreatitis 2019); 4. Voluntary signatories of informed consent Exclusion Criteria: 1. Patients with a history of diabetes mellitus or pre-diabetes mellitus, or glycosylated hemoglobin ≥ 6.0% or venous FPG ≥ 6.1 mmol/L at admission; 2. Patients have any evidence of type 1 diabetes-related autoimmunity; 3. Patients have any risk for secondary diabetes due to exposure to medications or other endocrine diseases; 4. Combined with pancreas-related trauma or a history of pancreatic surgery; 5. Patients undergo pancreatic surgery during treatment; 6. Pregnancy or breastfeeding; 7. Patients suffer from severe cardiac, hepatic or renal insufficiency or malignant diseases; 8. Failure to sign informed consent due to cognitive impairment or other conditions

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Shanghai Changzheng Hospital Shanghai Shanghai Municipality

More Shanghai Changzheng 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 NCT06590935 on ClinicalTrials.gov ↗ ← All trials in China