Overview

Efficacy of Perioperative Duloxetine as a Part of Multimodal Analgesia in Laparoscopic Colorectal Cancer Surgery

Status:
Not yet recruiting
Trial end date:
2021-04-01
Target enrollment:
0
Participant gender:
All
Summary
Our aim will be to evaluate the efficacy of perioperative Duloxetine in decreasing acute postoperative pain after laparoscopic colorectal cancer surgery and its role in reducing postoperative morphine requirements
Phase:
Phase 2
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Assiut University
Treatments:
Duloxetine Hydrochloride
Criteria
Inclusion Criteria:

- ASA I-III

- aged 18-65 years and scheduled for laparoscopic colorectal surgery for cancer colon

Exclusion Criteria:

- unable to express their pain or patient refusal.

- allergy to the study drug

- an abnormal liver or renal function tests

- a chronic opioid abuser(> 3 mo), being on chronic gabapentin or pregabalin(> 3 mo)

- antidepressant drugs, patients with psychiatric disorders

- Pregnant females