Combined leg nerve blocks for kids with cerebral palsy after surgery
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
Run by Diskapi Yildirim Beyazit Education and Research Hospital · NCT07801365 · Data updated 2026-11-12
This study tests whether adding two nerve blocks to standard anesthesia helps control pain in children with cerebral palsy after lower limb surgery.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 3 Years to 18 Years |
| Sex | All |
| Enrollment | 50 (estimated) |
| Sponsor | Diskapi Yildirim Beyazit Education and Research Hospital Government |
| Locations | 1 site (Ankara) |
| Status | Recruiting |
| Started | September 27, 2026 |
| Main results expected | September 14, 2027 |
| Study ends | September 27, 2027 |
| Registry record updated | October 29, 2026 |
| Trial ID | NCT07801365 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are children aged 3–18 years with cerebral palsy, ASA II–III, scheduled for elective lower-extremity surgery, and without contraindications to peripheral nerve blocks.
✕Probably not a fit
Patients with contraindications to regional anesthesia, infections at the block site, or who do not respond to regional techniques may not experience additional benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This prospective, randomized trial compares analgesia from combined ultrasound-guided popliteal sciatic nerve block and adductor canal block plus general anesthesia versus general anesthesia with intravenous analgesia alone in children with cerebral palsy undergoing elective lower-extremity procedures. Participants are aged 3–18 years and ASA II–III, and are assigned to intervention or control groups. Postoperative pain is measured with the r-FLACC scale at 1, 2, 6, 12, and 24 hours by an anesthesiologist blinded to group assignment. The study aims to determine if the nerve blocks provide superior pain relief and reduce analgesic needs without adding safety risks. The lead sponsor is Diskapi Yildirim Beyazit Education and Research Hospital, with the study conducted at Ankara Etlik City Hospital in Ankara, Turkey.
Why it matters
Potential benefit: If successful, children may experience better postoperative pain control and potentially lower use of systemic analgesics.
How similar studies have gone: Previous regional anesthesia studies in pediatric populations show potential for enhanced analgesia, but results can vary by procedure and patient condition.
Who can join: the full rules
Show full inclusion / exclusion criteria
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
Where it's running
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Ankara Etlik City Hospital
Ankara, Turkey (Türkiye) Recruiting
Study contacts
- Study coordinator: Elif Şule Özdemir Sezgi
- Email: elifsule-91@hotmail.com
- Phone: 00905059209638
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.