The Analgesic Efficacy of Wound Infiltration With Tramadol
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|ClinicalTrials.gov Identifier: NCT02518438|
Recruitment Status : Completed
First Posted : August 7, 2015
Last Update Posted : August 7, 2015
|Condition or disease||Intervention/treatment||Phase|
|Postoperative Pain||Drug: Tramadol||Phase 4|
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||60 participants|
|Intervention Model:||Crossover Assignment|
|Masking:||Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)|
|Official Title:||A Randomized Trial of the Analgesic Efficacy of Wound Infiltration With Tramadol After Cesarean Delivery Under General Anesthesia|
|Study Start Date :||May 2012|
|Actual Primary Completion Date :||March 2013|
|Actual Study Completion Date :||May 2013|
Active Comparator: the tramadol group
A preprepared 20 ml solution (tramadol 2 mgkg-1 within a 0.9% saline solution) was subcutaneously infiltrated after closure of the uterine incision and the rectus fascia.
A preprepared 20 ml solution was subcutaneously infiltrated after closure of the uterine incision and the rectus fascia.
Other Name: Placebo (0,9% saline solution)
Placebo Comparator: the placebo group
A preprepared 20 ml solution (0,9% saline solution) was subcutaneously infiltrated after closure of the uterine incision and the rectus fascia.
- The primary outcome measure in this study was cumulative morphine consumption. [ Time Frame: postoperative 24 hours ]The measure of need for analgesics in the immediate postoperative period in this study was cumulative morphine consumption.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02518438
|Yeditepe University Hospital|
|Istanbul, Kozyatagı, Turkey, 37452|