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NCT00819962 Clinical Trial

Perioperative Analgesia Using Ultrasound (US) Guided Transversus Abdominis Plane (TAP) Block

Postoperative Pain Clinical Trial

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT00819962
Other study ID # 08-652
Secondary ID
Status Recruiting
Phase Phase 0
First received January 6, 2009
Last updated September 13, 2015
Start date September 2014
Est. completion date December 2016

Study information
Verified date November 2014
Source King Saud University
Contact abdelazeem a dawlat, md
Phone 4692007
Email dawlatly@ksu.edu.sa
Is FDA regulated No
Health authority Saudi Arabia: Ethics Committee
Study type Interventional

Clinical Trial Summary

Perioperative analgesia using US guided TAP block

Description:

Perioperative analgesia using US guided TAP block

Recruitment information / eligibility
Status Recruiting
Enrollment 42
Est. completion date December 2016
Est. primary completion date December 2015
Accepts healthy volunteers No
Gender Both
Age group 20 Years to 50 Years
Eligibility Inclusion Criteria:

- adult undergoing laparoscopic cholecystectomy

Exclusion Criteria:

- history of cardiorespiratory disease

Study Design

Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Prevention

Related Conditions & MeSH terms

Intervention

Drug:
• Bupivacaine
Local anesthetic
Other:
• TAP

Locations
Country Name City State
Saudi Arabia A Dawlatly Riyadh
Saudi Arabia A Dawlatly Riyadh

Sponsors (1)
Lead Sponsor Collaborator
King Saud University

Country where clinical trial is conducted

Saudi Arabia, 

Outcome
Type Measure Description Time frame Safety issue
Primary Pain relief after US TAP block Yes
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