Clinical Trials Directory

Trials / Completed

CompletedNCT02518438

The Analgesic Efficacy of Wound Infiltration With Tramadol

A Randomized Trial of the Analgesic Efficacy of Wound Infiltration With Tramadol After Cesarean Delivery Under General Anesthesia

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
60 (actual)
Sponsor
Yeditepe University Hospital · Academic / Other
Sex
Female
Age
18 Years – 35 Years
Healthy volunteers
Accepted

Summary

This double-blind, randomized trial examined whether tramadol wound infiltration decreased postoperative pain following cesarean delivery under general anesthesia or reduced the need for analgesics in the immediate postoperative period. Patients in the tramadol group consumed significantly less morphine at all time intervals than those in the control group. The investigators suggest that the use of wound infiltration with tramadol may be a useful technique in patients who undergo cesarean section under general anesthesia to reduce postoperative pain, improve recovery, and facilitate early contact of mothers with their babies.

Conditions

Interventions

TypeNameDescription
DRUGTramadolA preprepared 20 ml solution was subcutaneously infiltrated after closure of the uterine incision and the rectus fascia.

Timeline

Start date
2012-05-01
Primary completion
2013-03-01
Completion
2013-05-01
First posted
2015-08-07
Last updated
2015-08-07

Locations

1 site across 1 country: Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT02518438. Inclusion in this directory is not an endorsement.

The Analgesic Efficacy of Wound Infiltration With Tramadol (NCT02518438) · Clinical Trials Directory