ltrasound-guided transversus abdominis plane block versus caudal block for pain relief in childre

Phase 2

Completed

• Conditions: Postoperative PainAnesthesia; Postoperative Pain; Anesthesia; Anaesthesiology - Pain management

• Registration Number: ACTRN12612001074886
• Lead Sponsor: Yusheng Yao

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2012-10-08
• Last Update Posted: 13 January 2020

Recruitment & Eligibility

• Status: Completed
• Sex: Male
• Target Recruitment: 80

Inclusion Criteria

ASA ststus I-II aged 2-5yr undergoing unilateral inguinal hernia repair

Exclusion Criteria

Hypersensitivity to any local anesthetics
Infections at puncture sites
Bleeding diathesis
Preexisting neurological disease

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Time to first rescue medication[From the data of intervention until the data of the first registration of a CHIPPS scores larger than 3, assessed up to 24h];the number of patients not requiring rescue analgesia[After surgery, up to 24h]