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Perioperative Duloxetine for Pain Management After Laparoscopic Hysterectomy

NCT03350334 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 100

Last updated 2018-05-16

No results posted yet for this study

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.

Conditions

  • Laparoscopic Hysterectomy
  • Postoperative Recovery
  • Postoperative Pain

Interventions

DRUG

Duloxetine

Peri-operative Duloxetine administration

DRUG

placebo

Placebo administration

Sponsors & Collaborators

  • Acibadem University

    lead OTHER

Principal Investigators

  • Mete Gungor, MD,Prof · Acibadem Maslak Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-12-04
Primary Completion
2018-03-10
Completion
2018-03-15

Countries

  • Turkey (Türkiye)

Study Locations

More Related Trials

Entities

Drugs

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03350334 on ClinicalTrials.gov