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NCT00964600 Clinical Trial

Bilateral Transversus Abdominis Plane Block and Postoperative Pain Intensity After Elective Cesarean Delivery

Postoperative Pain Clinical Trial

— TAP  

Official title:
Evaluation of the Effect of Bilateral Transversus Abdominis Plane Block on Postoperative Pain Intensity and Analgesia Consumption After Elective Cesarean Delivery

Clinical Trial Details — Status: Unknown status

Administrative data
NCT number NCT00964600
Other study ID # 825
Secondary ID
Status Unknown status
Phase N/A
First received August 20, 2009
Last updated November 17, 2010
Start date September 2008
Est. completion date October 2009

Study information
Verified date November 2010
Source Tehran University of Medical Sciences
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The patients planned to go under elective cesarean delivery under general anesthesia are randomly assigned to have either bilateral transversus abdominis plane (TAP) block or usual standard analgesics after cesarean. Pain score (Verbal Analog Scale VAS) and analgesic requirements are recorded. It's supposed that both are significantly reduced in patients undergoing TAP block.

Recruitment information / eligibility
Status Unknown status
Enrollment 60
Est. completion date October 2009
Est. primary completion date September 2009
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria:

1. Elective cesarean delivery

2. Term pregnancies

3. General anesthesia

4. Pfannenstiel incision

Exclusion Criteria:

1. No history of sensitivity to prescribed analgesic (Bupivacaine or related substances)

2. No preeclampsia

3. No history of psychologic disorders

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• TAP blockade
15 cc Bupivacaine 0.25% ,injected bilaterally in the TAP blockade arm

Locations
Country Name City State
Iran, Islamic Republic of Sharati hospital Tehran

Sponsors (1)
Lead Sponsor Collaborator
Tehran University of Medical Sciences

Country where clinical trial is conducted

Iran, Islamic Republic of, 

Outcome
Type Measure Description Time frame Safety issue
Primary Pain intensity after cesarean section one year
Secondary Analgesic prescribed measurement one year
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