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

Sponsor
King Saud University (Other)
Overall Status
Unknown status
CT.gov ID
NCT00819962
Collaborator
(none)
42
2
1
27
21
0.8

Study Details

Study Description

Brief Summary

Perioperative analgesia using US guided TAP block

Condition or Disease Intervention/Treatment Phase
Early Phase 1

Detailed Description

Perioperative analgesia using US guided TAP block

Study Design

Study Type:
Interventional
Anticipated Enrollment :
42 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Masking:
Double (Participant, Investigator)
Primary Purpose:
Prevention
Study Start Date :
Sep 1, 2014
Anticipated Primary Completion Date :
Dec 1, 2015
Anticipated Study Completion Date :
Dec 1, 2016

Arms and Interventions

Arm Intervention/Treatment
Other: TAP

ksu

Drug: Bupivacaine
Local anesthetic

Other: TAP

Outcome Measures

Primary Outcome Measures

  1. Pain relief [after US TAP block]

Eligibility Criteria

Criteria

Ages Eligible for Study:
20 Years to 50 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • adult undergoing laparoscopic cholecystectomy
Exclusion Criteria:
  • history of cardiorespiratory disease

Contacts and Locations

Locations

Site City State Country Postal Code
1 A Dawlatly Riyadh Saudi Arabia
2 A Dawlatly Riyadh Saudi Arabia

Sponsors and Collaborators

  • King Saud University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
A.Eldawlatly, Professor of Anesthesia, King Saud University
ClinicalTrials.gov Identifier:
NCT00819962
Other Study ID Numbers:
  • 08-652
First Posted:
Jan 9, 2009
Last Update Posted:
Sep 15, 2015
Last Verified:
Nov 1, 2014
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 15, 2015