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

The recruitment status of this study is unknown because the information has not been verified recently.

Verified January 2009 by King Saud University.
Recruitment status was Not yet recruiting

Sponsor:

Information provided by:

King Saud University

ClinicalTrials.gov Identifier:

NCT00819962

First received: January 6, 2009

Last updated: January 8, 2009

Last verified: January 2009

History of Changes

Tracking Information
First Received Date ^ICMJE	January 6, 2009
Last Updated Date	January 8, 2009
Start Date ^ICMJE	February 2009
Estimated Primary Completion Date	July 2009 (final data collection date for primary outcome measure)
Current Primary Outcome Measures ^ICMJE (submitted: January 8, 2009)	Pain relief [ Time Frame: after US TAP block ] [ Designated as safety issue: Yes ]
Original Primary Outcome Measures ^ICMJE	Same as current
Change History	Complete list of historical versions of study NCT00819962 on ClinicalTrials.gov Archive Site
Current Secondary Outcome Measures ^ICMJE	Not Provided
Original Secondary Outcome Measures ^ICMJE	Not Provided
Current Other Outcome Measures ^ICMJE	Not Provided
Original Other Outcome Measures ^ICMJE	Not Provided

Descriptive Information
Brief Title ^ICMJE	Perioperative Analgesia Using Ultrasound (US) Guided Transversus Abdominis Plane (TAP) Block
Official Title ^ICMJE	Not Provided
Brief Summary	Perioperative analgesia using US guided TAP block
Detailed Description	Perioperative analgesia using US guided TAP block
Study Type ^ICMJE	Interventional
Study Phase	Phase 0
Study Design ^ICMJE	Allocation: Randomized Endpoint Classification: Safety Study Intervention Model: Crossover Assignment Masking: Double Blind (Subject, Investigator) Primary Purpose: Prevention
Condition ^ICMJE	Postoperative Pain
Intervention ^ICMJE	Drug: Bupivacaine Local anesthetic
Study Arm (s)	Not Provided
Publications *	Not Provided
* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.

Recruitment Information
Recruitment Status ^ICMJE	Not yet recruiting
Estimated Enrollment ^ICMJE	42
Completion Date	Not Provided
Estimated Primary Completion Date	July 2009 (final data collection date for primary outcome measure)
Eligibility Criteria ^ICMJE	Inclusion Criteria: adult undergoing laparoscopic cholecystectomy Exclusion Criteria: history of cardiorespiratory disease
Gender	Both
Ages	20 Years to 50 Years
Accepts Healthy Volunteers	No
Contacts ^ICMJE	Not Provided
Location Countries ^ICMJE	Not Provided

Administrative Information
NCT Number ^ICMJE	NCT00819962
Other Study ID Numbers ^ICMJE	08-652
Has Data Monitoring Committee	Not Provided
Responsible Party	CMRC, KSU
Study Sponsor ^ICMJE	King Saud University
Collaborators ^ICMJE	Not Provided
Investigators ^ICMJE	Not Provided
Information Provided By	King Saud University
Verification Date	January 2009
^ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP

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