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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT02854553
Other study ID # TAP in liposuction
Secondary ID
Status Not yet recruiting
Phase N/A
First received July 30, 2016
Last updated August 2, 2016
Start date September 2016
Est. completion date September 2017

Study information

Verified date July 2016
Source Cairo University
Contact Hassan Ali, lecturer
Phone 1001733687
Email hassan364@hotmail.com
Is FDA regulated No
Health authority Egypt: Ministry of Higher Education
Study type Interventional

Clinical Trial Summary

The transversus abdominis plane (TAP) block is an effective regional nerve block for the anterior abdominal wall. An anesthesiologist typically administers the TAP block preoperatively with ultrasound guidance. It is not yet commonly used during anterior abdominal wall liposuction, where postprocedural pain remains a major concern for patients and surgeons.


Description:

The author investigated the feasibility of administering the TAP block under direct vision and compared postoperative narcotic use in patients who received analgesia by TAP block vs with TAP block i addition to rectus sheath block, both performed under direct vision during anterior abdominal wall liposuction.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 48
Est. completion date September 2017
Est. primary completion date September 2017
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- ASA I-II, consent,

Exclusion Criteria:

- allergy, coagulopathy, refusal, mentally unstable

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Procedure:
Transversus abdominis plane block
ultra sound guides Transversus abdominis plane block
rectus sheath block
ultrasound guided rectus sheath block

Locations

Country Name City State
Egypt Cairo University Cairo Giza

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary pain visual analogue scale for pain assessment Three days Yes
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