ltrasound-Guided Abdominal Wall Nerve Block

Phase 4

• Conditions: Patients undergoing abdominoplasty surgery; Abdominoplasty; Pain Relief; Nerve Block; Opioids; Local Anesthesia

• Registration Number: TCTR20210712002
• Lead Sponsor: AlKindi Specialised Hospital, Bahrain

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2021-07-12
• Study Completion: 2021-11-25
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Pending (Not yet recruiting)
• Sex: All
• Target Recruitment: 75

Inclusion Criteria

Patients undergoing abdominoplasty surgery with rictus sheath plication
ASA I-II patients

Exclusion Criteria

Patients refusal
Patient with history of known hypersensitivity of local anesthetic
Psychiatric disorders and or use of psychiatric medications

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Opioids consumption Postoperative patient admission period Dose per mg

Secondary Outcome Measures

Name	Time	Method
Postoperative pain Postoperative patient admission period Degree of pain,Postoperative time for patient first ambulation Postoperative patient admission period Time per hour,Postoperative time for patient incentive spirometer 900 ml/min Postoperative patient admission period Time per hour