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 University162 enrolled

Overview

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.

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).

Study Type

OBSERVATIONAL

Enrollment

162

Conditions

Postoperative Pain

Interventions

CelecoxibDRUG

Patients in ERAS group received celecoxib

Eligibility

Sex: ALL

Medical Language ↔ Plain English

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.

Locations (1)

Sasikaan Nimmaanrat

Hat Yai, Changwat Songkhla, Thailand

RECRUITING

Outcomes

Primary Outcomes

Pain intensity

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

Time frame: Until discharge (5-7 days)

Secondary Outcomes

Opioid

Amount of postoperative opioid consumption

Time frame: Until discharge (5-7 days)

Central Contacts

Sasikaan Nimmaanrat, MD

CONTACT

+66887907842 snimmaanrat@yahoo.com.au

Data from ClinicalTrials.gov

This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.