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Perioperative Duloxetine for Pain Management After Laparoscopic Hysterectomy

Postoperative Pain Clinical Trial

Official title:
Perioperative Duloxetine for Pain Management After Laparoscopic Hysterectomy: A Prospective Randomized Placebo-controlled Study

Clinical Trial Summary

The aim of the investigators of the study is to evaluate the effect of peri-operative duloxetine on post-operative recovery in patients undergoing laparoscopic hysterectomy.

Clinical Trial Description

Patients with benign gynecologic conditions (fibroids, pelvic pain, uterine prolapse) who are planned to undergo laparoscopic hysterectomy will be enrolled in the study. After randomization, the study participants will be given 60 mg duloxetine 2 hours before surgery and 24 hours after surgery, whereas the control participants will be given placebo tablets. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03350334
Study type Interventional
Source Acibadem University
Contact
Status Completed
Phase N/A
Start date December 4, 2017
Completion date March 15, 2018
View Details
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