drugset / Trial / NCT04989166

Effect of Nano-curcumin Supplementation in Acute Pancreatitis

NCT04989166

RandomizedParallel-groupDouble-blindTreatment

Summary

This study aims to investigate the effect of nano-curcumin supplementation on hospital length of stay, clinical outcomes, and inflammation level in mild and moderate acute pancreatitis. 42 eligible patients with mild and moderate acute pancreatitis will randomly assign to consume two soft gels each containing 40 mg of nano-curcumin or placebo (control group) every morning and evening for two weeks. Both groups will also receive the standard medical treatment of acute pancreatitis according to relevant guidelines. Patient's blood samples and clinical outcomes will assess on days 0, 1, 2, 3, 4, and 14 of admission. The two groups will also be compared in terms of adverse events and hospital length of stay. Moreover, the patient's hospital readmission due to pancreatitis will be recorded within 90 days of hospitalization.

Timeline

Start
2021-10-19
Primary completion
2022-10-15
Completion
2023-01-15

Drugs

EvaluationDrugModalityDoseRoute
Subject Nanocurcumin Unknown 40 mg

Indications