Endocrine and exocrine dysfunction in patients after developing acute pancreatitis
Not Applicable
- Conditions
- Health Condition 1: K859- Acute pancreatitis, unspecified
- Registration Number
- CTRI/2020/09/027962
- Lead Sponsor
- Jayanta Samanta
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Patients who gave informed consent for participation in the study
2.Patients with age >= 16 years
3. Patients who had a past history of acute pancreatitis
Exclusion Criteria
1.A patient who has suffered recurrent episodes of AP.
2.Patients with chronic pancreatitis.
3.Patient with diagnosed diabetes mellitus before acute pancreatitis episode
4.Patients suffering from chronic diarrhea before AP
5.Patient with intestinal tuberculosis or Crohnâ??s disease
6.Patients who died during hospitalization
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To assess the incidence of endocrine and exocrine pancreatic insufficiency after acute pancreatitis.Timepoint: At 1 month, 3 months after the episode of acute pancreatitis
- Secondary Outcome Measures
Name Time Method 1.To assess the risk factors of exocrine and endocrine pancreatic insufficiency after first attack of acute pancreatitis. <br/ ><br>2.To assess the effect of necrosectomy (using percutaneous drainage or surgical) on the development of exocrine and endocrine pancreatic insufficiency <br/ ><br>3.To assess the short term (at 6 months) persistent of exocrine and endocrine pancreatic insufficiency after discharge. <br/ ><br>Timepoint: At 1 month, 3 months and 6 months after the episode of acute pancreatitis