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

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified November 2014 by A.Eldawlatly, King Saud University.
Recruitment status was:  Recruiting
Sponsor:
ClinicalTrials.gov Identifier:
NCT00819962
First Posted: January 9, 2009
Last Update Posted: September 15, 2015
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
A.Eldawlatly, King Saud University
  Purpose
Perioperative analgesia using US guided TAP block

Condition Intervention Phase
Postoperative Pain Drug: Bupivacaine Other: TAP Early Phase 1

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Crossover Assignment
Masking: Double (Participant, Investigator)
Primary Purpose: Prevention

Resource links provided by NLM:


Further study details as provided by A.Eldawlatly, King Saud University:

Primary Outcome Measures:
  • Pain relief [ Time Frame: after US TAP block ]

Estimated Enrollment: 42
Study Start Date: September 2014
Estimated Study Completion Date: December 2016
Estimated Primary Completion Date: December 2015 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
TAP
ksu
Drug: Bupivacaine
Local anesthetic
Other: TAP

Detailed Description:
Perioperative analgesia using US guided TAP block
  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   20 Years to 50 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • adult undergoing laparoscopic cholecystectomy

Exclusion Criteria:

  • history of cardiorespiratory disease
  Contacts and Locations
Information from the National Library of Medicine

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): NCT00819962


Contacts
Contact: abdelazeem a dawlat, md 4692007 dawlatly@ksu.edu.sa

Locations
Saudi Arabia
A Dawlatly Recruiting
Riyadh, Saudi Arabia
Contact: a dawlatly a abdelaz    00966 503261042    dawlatly@ksu.edu.sa   
Principal Investigator: a a daw, md         
A Dawlatly Recruiting
Riyadh, Saudi Arabia
Contact: a dawlatly a abdelaz         
Principal Investigator: a a daw, md         
Sponsors and Collaborators
King Saud University
  More Information

Responsible Party: A.Eldawlatly, Professor of Anesthesia, King Saud University
ClinicalTrials.gov Identifier: NCT00819962     History of Changes
Other Study ID Numbers: 08-652
First Submitted: January 6, 2009
First Posted: January 9, 2009
Last Update Posted: September 15, 2015
Last Verified: November 2014

Additional relevant MeSH terms:
Pain, Postoperative
Pain
Neurologic Manifestations
Nervous System Diseases
Postoperative Complications
Pathologic Processes
Signs and Symptoms
Bupivacaine
Anesthetics, Local
Anesthetics
Central Nervous System Depressants
Physiological Effects of Drugs
Sensory System Agents
Peripheral Nervous System Agents