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Clinical Trials in China / NCT06230432
Starting soon Observational

Exploring the Mechanism of Severe Acute Pancreatitis Based on Metagenomics, Metabolomics and Proteomics

NCT06230432 · tracked via the Priya Life Science China tracker
Sponsor
The First Affiliated Hospital of Nanchang University
Phase
Observational
Started
2024-01-21
Last updated
2024-01-30

Condition(s) studied

Acute Pancreatitis

Study summary

The goal of this observational study is to learn about the biomarkers and mechanisms of severe acute pancreatitis in 30 healthy controls, 30 patients of mild acute pancreatitis, 30 patients of moderately severe acute pancreatitis, and 86 patients of severe acute pancreatitis. The main question it aims to answer are: • The relationship between changes in gut microbiota and clinical prognosis (plasma inflammatory cytokines, incidence and duration of infection in various parts, mortality rate), and the screening and validation of biomarkers that can be used for early prediction of disease severity. • Analyze the relationship between changes in blood composition and clinical prognosis (plasma inflammatory cytokines, incidence and duration of infection in various parts, mortality rate), screen and verify biomarkers that can be used for early prediction of disease severity. Blood and fecal samples from the healthy control group and diagnosed patients will be collected.

Eligibility

Sex
ALL
Min age
18 Years
Max age
75 Years
Healthy volunteers
Accepted
Inclusion Criteria: Patients group: ① Age between 18 and 75 years old; ② Within 72 hours of AP onset; ③ AP patients who meet the 2012 Atlanta AP Classification and Diagnostic Criteria. Healthy control group: * Age between 18 and 75 years old; ② No history of acute pancreatitis; ③ Routine laboratory tests such as blood routine and fecal routine are normal. Exclusion Criteria: * Used antibiotics, probiotics, and acid suppressants 4 weeks before enrollment; * Pregnant and lactating women; * Hypothyroidism, nephrotic syndrome, Cushing's syndrome, AIDS; * Chronic pancreatitis, pancreatic cancer; ⑤ Severe history of cardiovascular and cerebrovascular diseases and organ dysfunction, such as malignant tumors, heart failure, coronary heart disease, chronic obstructive pulmonary disease, liver and kidney failure; ⑥ Unsigned informed consent form.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
The First Affiliated Hospital of Nanchang University Nanchang Jiangxi

More The First Affiliated Hospital of Nanchang University 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 NCT06230432 on ClinicalTrials.gov ↗ ← All trials in China