Treatment of Acute Pancreatitis With Ketorolac

Status Terminated

Clinical Trial Summary

Patients with acute pancreatitis will be randomly assigned in either study group to receive oral (injection) Ketorolac or the control group. In patients who cannot tolerate oral medications, ketorolac injection will be used.

Clinical Trial Description

Patients with acute pancreatitis will be randomly assigned in either study group or control group.

- The study group will receive injection or oral Ketorolac.

- The control group will receive standard medical treatment.

Ketorolac is administrated three times daily by mouth or injection starting from the time of admission for the first three days of hospitalization (72 hours).

Hs-CRP will be measured in admission in addition to standard laboratory tests.It will be done every day for up to 5 days, after the administration of study drug or till the time of discharge whichever occurs earlier. Patients will follow up for organ failure involvement and duration of hospitalization. The study will continue to gather clinical follow up information up to four months. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02885441
Study type	Interventional
Source	Ilam University of Medical Sciences
Contact
Status	Terminated
Phase	Phase 4
Start date	September 2016
Completion date	February 1, 2019

View Details

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