Transversus Abdominis Plane Block levobupivacaine plus ketamine in abdominoplasty

Not Applicable

Recruiting

• Conditions: Surgery; perio-perative analgesia; Anaesthesia

• Registration Number: PACTR201703002081320
• Lead Sponsor: Tanta University hospitals

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2017-03-07
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 50

Inclusion Criteria

Patients of American Society of Anesthesiologist (I, II), aged from 25 to 50 year of both sex undergoing abdominoplasty will be enrolled in the study

Exclusion Criteria

Body mass index ¿¿BMI¿¿ > 35 kg/m2, allergies to local anesthetic, alcohol or drug abuse, coagulation disorders, mental or physical illness interfere with evaluation of VAS

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Postoperative pain

Secondary Outcome Measures

Name	Time	Method
Overall patient satisfaction