Overview
Efficacy of Perioperative Duloxetine as a Part of Multimodal Analgesia in Laparoscopic Colorectal Cancer Surgery
Status:
Not yet recruiting
Not yet recruiting
Trial end date:
2021-04-01
2021-04-01
Target enrollment:
0
0
Participant gender:
All
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 requirementsPhase:
Phase 2Accepts Healthy Volunteers?
Accepts Healthy VolunteersDetails
Lead Sponsor:
Assiut UniversityTreatments:
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