Viewing Study NCT02790203


Ignite Creation Date: 2025-12-24 @ 7:32 PM
Ignite Modification Date: 2026-03-01 @ 3:23 PM
Study NCT ID: NCT02790203
Status: UNKNOWN
Last Update Posted: 2016-06-03
First Post: 2016-05-22
Is Gene Therapy: True
Has Adverse Events: False

Brief Title: Perioperative Use of a Selective COX2 Inhibitor in Patients Undergoing Elective Colorectal Surgery: the Effect on Post-operative Bowel Motility and Post-operative Pain
Sponsor: Sheba Medical Center
Organization:

Study Overview

Official Title: None
Status: UNKNOWN
Status Verified Date: 2016-05
Last Known Status: NOT_YET_RECRUITING
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: Perioperative Celecoxib to promote bowel movement and to reduce post-operative pain after elective colonic resection.
Detailed Description: Post-operative ileus is a common surgical complication occurring in with up to 20% of patients, with a significant clinical and economical effect.

Many preventative measures have been tested to promote gastrointestinal motility following intestinal surgery have been suggested.

The medical intervention in the proposed study includes administration of a selective COX-2 inhibitor, specifically Celecoxib, in the peri-operative period following an elective colon resection. Celecoxib is a nonsteroidal anti-inflammatory drug (NSAID) with anti-inflammatory, analgesic, and antipyretic therapeutic effects.

The drug is approved for use in by the ministry of health in Israel and in the United states. The study aims to assess the use of this widely used medication for evaluation of the clinical effect on post-operative bowel transit, as well as the drugs' effect on post-operative pain.

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: