Comparison between caudal block and lateral sciatic nerve block for lower extremity surgery in pediatric patients.

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

TCTR

Registry ID

TCTR20190914003

Enrollment

Registered

2019-09-14

Start date

2019-09-12

Completion date

Unknown

Last updated

2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

post operative pain caudal block lateral sciatic nerve block efficiency

Interventions

caudal block 0.25% marcaine with ADR (1:200&#44

000) dose 0.5 ml/kg,ultrasound guided lateral sciatic n block 0.25% marcaine with ADR (1:200&#44

000) dose 0.5 ml/kg

Active Comparator Procedure/Surgery,Active Comparator Procedure/Surgery

caudal block, lateral sciatic n block

Eligibility

Sex/Gender

All

Age

1 Years to 10 Years

Inclusion criteria

Inclusion criteria: - Pediatric patients of either sex, between 1 to 10 years - ASA classification 1-3 - Scheduled for lower extremity surgery (covered with lateral sciatic nerve), under general anesthesia - Inform consent - Participate only in this research

Exclusion criteria

Exclusion criteria: - Allergy to amide-type local anaesthetics - Skin infection at leg - The presence of a sacral dimple - Coagulopathy

Design outcomes

Primary

Measure	Time frame
To evaluate the quality of analgesia after surgery, 30 mins, 2 hrs, 4 hrs, 8 hrs, 18 hrs Post-operative pain score (FLACC scale,Faces Pain Scale,Numeric rating scale,FLARR))	—

Secondary

Measure	Time frame
To compare the duration of postoperative analgesia after the surgery hours and micrograms,To compare opioid consumption in the first 24 postoperative hours after surgery in 24 hrs micrograms	—

Countries

Thailand

Contacts

Public Contactkamolmal charoenarparasmee

digidigi_bee@hotmail.com0850887955

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026