Comparison of Postoperative Pain Management in Patients Undergoing Laparoscopic Colorectal Surgery Under Enhanced Recovery After Surgery (ERAS) Program, Laparoscopic Colorectal Surgery Without ERAS and Open Colorectal Surgery
Overview
- Phase
- Not Applicable
- Intervention
- Celecoxib
- Conditions
- Postoperative Pain
- Sponsor
- Prince of Songkla University
- Enrollment
- 162
- Locations
- 1
- Primary Endpoint
- Pain intensity
- Last Updated
- 4 years ago
Overview
Brief Summary
This is a retrospective study to compare postoperative pain intensity in patients going laparoscopic colorectal surgery with Enhanced Recovery after Surgery (ERAS), without ERAS and open colorectal surgery.
Detailed Description
This study is a matched case-control study. Control patients will be matched to ERAS cases in a 1:1:1 ratio (laparoscopic surgery with ERAS protocol : laparoscopic surgery without ERAS protocol : open surgery).
Investigators
Sasikaan Nimmaanrat
Associate Professor
Prince of Songkla University
Eligibility Criteria
Inclusion Criteria
- •Patients undergoing colorectal surgery under ERAS program and those with the same sort of laparoscopic surgery without ERAS program as well as those with open colorectal surgery with complete required recorded data.
Exclusion Criteria
- •Patients with incomplete required data on record.
- •Those with any major intraoperative or postoperative complications.
Arms & Interventions
ERAS
Patients undergoing laparoscopic colorectal surgery with ERAS
Intervention: Celecoxib
Outcomes
Primary Outcomes
Pain intensity
Time Frame: Until discharge (5-7 days)
Pain score (Verbal Numerical Rating Scale: VNRS) after surgery, VNRS consists of 0-10, where 0 means no pain and 10 means worst pain imaginable
Secondary Outcomes
- Opioid(Until discharge (5-7 days))