Effect of Preoperative Duloxetine on Quality of Recovery After Outpatient Laparoscopic Surgery

Withdrawn before enrolling · Phase 4 · Has a placebo group

Conditions studied: Quality of Recovery, Gynecologic Surgery, Laparoscopy

In brief

The objective of this study is to determine the effect of preoperative duloxetine on postoperative quality of recovery after ambulatory surgery, specifically laparoscopic gynecological surgery.

Key facts

Study ID

NCT02351440

Run by

Northwestern University

People needed

0

Starts

2016-04-01

Expected to finish

2017-08-31

Last updated by the study team

2018-08-21

Who can join

Age: 18 and older, up to 65. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• outpatient gynecological laparoscopy
• ASA PS 1 and 2
• fluent in English

You may not qualify if…

• history of allergy to duloxetine, history of chronic opioid use, pregnant patients, preoperative SSRI or SNRI use, prolonged QT interval on ECG

Where it is running

• Prentice Womens Hospital — Chicago, Illinois, United States

Full record on ClinicalTrials.gov

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