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Study of Peripheral Blood Non-coding RNAs as Diagnosis and Prognosis Biomarker for Acute Pancreatitis (NCRNAP)

N

Naval Military Medical University

Status

Completed

Conditions

Acute Pancreatitis

Study type

Observational

Funder types

Other

Identifiers

NCT02602808
Pancreatitis Markers

Details and patient eligibility

About

It is important to identify patients with acute pancreatitis who are at risk for developing persistent organ failure early in the course of disease. The investigators evaluated whether peripheral blood non-coding RNAs, including microRNAs and long noncoding RNA (lncRNA), could serve as a good marker for detection of acute pancreatitis with persistent organ failure at early phase.

Full description

Acute pancreatitis is a sudden inflammation of the pancreas. It can have severe complications and high mortality despite treatment. While mild cases are often successfully treated with conservative measures, such as fasting and aggressive intravenous fluid rehydration, severe cases may require admission to the intensive care unit or even surgery to deal with complications of the disease process. The diagnosis of severe acute pancreatitis at an early phase remain a major challenge for clinicians.

Therefore, many biologic markers have been studied in an effort to improve the diagnostic rate and determine the severity of acute pancreatitis but with disappointing results. Non-coding RNAs, including microRNAs and long noncoding RNA (lncRNA), have recently been validated to stably exist in peripheral blood. Several publications showed that it may serve as potential markers for various diseases, including cancer and inflammation. Our current study evaluated whether and which kind of non-coding RNAs could serve as good markers for severe acute pancreatitis.

Enrollment

1,097 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients who was diagnosed acute pancreatitis
  • Male or female
  • 18 Years and older
  • written informed consent

Exclusion criteria

  • Symptoms of acute pancreatitis present for more than 72 hours
  • Age under 18 years
  • Pregnancy
  • patients unable to consent

Trial design

1,097 participants in 4 patient groups

Severe acute pancreatitis group
Description:
Severe acute pancreatitis is characterised by persistent organ failure.
Moderately severe acute pancreatitis
Description:
Moderately severe acute pancreatitis is characterised by the presence of transient organ failure or local or systemic complications in the absence of persistent organ failure.
Mild acute pancreatitis
Description:
Mild acute pancreatitis is characterised by the absence of organ failure and the absence of local or systemic complications.
post-ERCP pancreatitis
Description:
Patients with new onset of epigastric pain, an increase in pancreatic enzymes of at least three times the upper limit of the normal range within 24 hours after ERCP, and hospitalization for at least 2 nights.

Trial contacts and locations

3

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Data sourced from clinicaltrials.gov

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