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
| Type | Name | Description |
|---|---|---|
| DRUG | Tramadol | A 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.