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

Prince of Songkla University

Status: Unknown

Conditions: Postoperative Pain

Treatments: Drug: Celecoxib

Study type: Observational

Funder types: Other

Identifiers

NCT04997174

REC.64-290-8-1

Details and patient eligibility

About

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.

Full 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).

Enrollment: 162 estimated patients

Sex: All

Volunteers: No Healthy Volunteers

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

• 1. Patients with incomplete required data on record.
• 2. Those with any major intraoperative or postoperative complications.

Trial design

162 participants in 3 patient groups

ERAS

Description:

Patients undergoing laparoscopic colorectal surgery with ERAS

Treatment:

Drug: Celecoxib

Non ERAS

Description:

Patients undergoing laparoscopic colorectal surgery without ERAS

Open

Description:

Patients undergoing open colorectal surgery