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Clinical Trials/NCT03634787
NCT03634787UnknownNot Applicable

Heat Shock Proteins: a Pathogenic Driver and Potential Therapeutic Target in Acute Pancreatitis

Vilnius University1 site in 1 country280 target enrollmentStarted: October 20, 2017Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Enrollment
280
Locations
1
Primary Endpoint
To measure the levels of heat shock proteins in serum and plasma in acute severe pancreatitis settings

Study Overview

Brief Summary

To investigate the role of Heat Shock Proteins in the mechanism of acute severe pancreatitis. In addition to test the potential treatment target of acute pancreatitis.

All patients who present with clinical symptoms of acute pancreatitis are evaluated for the enrollment of the study.

Detailed Description

All patients with acute pancreatitis are evaluated according to modified Atlanta classification acute pancreatitis severity scores.

Blood serum, urine and DNA samples are collected from all patients presented on admission, after 24 hours, 48 hours, 72 hours.

CT is performed in al patients to evaluate necrosis of pancreas Day 5-7 since hospital admission. If necrosis is not present follow-up is stopped.

Study Design

Study Type
Observational
Observational Model
Case Control
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to 100 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • no prior diagnosis of acute pancreatitis
  • admission to the hospital within 2 days since the clinical symptoms
  • confirmed diagnosis of acute pancreatitis

Exclusion Criteria

  • chronic pancreatitis
  • pancreatic cancer

Outcomes

Primary Outcomes

To measure the levels of heat shock proteins in serum and plasma in acute severe pancreatitis settings

Time Frame: 2 years

Different molecular weight Heat Shock proteins role while developing acute pancreatitis.

Secondary Outcomes

  • To measure pancreas cells activity while applying Heat Shock Protein inhibitors(2 years)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Aiste Gulla

Senior surgery resident

Vilnius University

Study Sites (1)

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