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Combined Popliteal and Adductor Canal Blocks for Postoperative Analgesia in Children With Cerebral Palsy

Not yet recruitingNot applicableNCT07801365
View the official record on ClinicalTrials.gov

Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.

This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.

Brief summary (from the registry)

This prospective, randomized, controlled trial aims to evaluate the postoperative analgesic efficacy of combined ultrasound-guided popliteal sciatic nerve block and adductor canal block in children with cerebral palsy undergoing elective lower extremity surgery. Children aged 3-18 years with American Society of Anesthesiologists (ASA) physical status II-III will be randomized into two groups. Participants in the intervention group will receive combined popliteal sciatic nerve block and adductor canal block in addition to general anesthesia, whereas participants in the control group will receive general anesthesia with intravenous analgesia without peripheral nerve block. Postoperative pain will be assessed using the revised Face, Legs, Activity, Cry, Consolability (r-FLACC) scale at 1, 2, 6, 12, and 24 hours after surgery by an anesthesiologist blinded to group allocation.

Study details

Official title
Postoperative Analgesic Efficacy of Combined Popliteal and Adductor Canal Blocks in Children With Cerebral Palsy Undergoing Lower Extremity Surgery: A Randomized Controlled Trial
Interventions
  • Procedure: Adductor Canal Block + Popliteal Sciatic Nerve Block Group
  • Procedure: Control Group
Sponsor
Diskapi Yildirim Beyazit Education and Research Hospital
Start date
2026-09-14
Primary completion
2027-09-14
Sex
All
Age range
from 3 Years to 18 Years
Results posted
No results posted in this snapshot
Countries
Turkey (Türkiye)
Total sites listed
1

Eligibility criteria

Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * Pediatric patients aged 3-18 years * Diagnosis of cerebral palsy * Scheduled to undergo lower extremity surgery * American Society of Anesthesiologists (ASA) physical status II-III * Scheduled for elective surgery * Written informed consent obtained from a parent or legal guardian Exclusion Criteria: * Age younger than 3 years or older than 18 years * Coagulopathy or any contraindication to peripheral nerve block * Known allergy to local anesthetics * Infection at the planned block site

Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT07801365