Clinical trial Recruiting at 1 site Interventional Ages 12 Months to 12

Pain relief for high-risk children after anorectal and penile surgery using a targeted nerve block

Official title: Efficacy of Ultrasound-guided Sacral Multifidus Plane Block as Perioperative Analgesia for Anal and Penile Surgeries in High-risk Pediatric Patients

Run by Zagazig University · NCT07602894 · Data updated 2026-11-12

This study tests whether ultrasound-guided sacral multifidus plane blocks can provide safe, effective pain relief for high-risk pediatric patients undergoing anorectal and penile surgeries.

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Quick facts

Study typeInterventional
Ages12 Months to 12 Years
SexAll
Enrollment60 (estimated)
SponsorZagazig University
Government
Locations1 site (Zagazig)
StatusRecruiting
StartedJuly 20, 2026
Main results expectedJuly 2027
Study endsDecember 2027
Registry record updatedAugust 24, 2026
Trial IDNCT07602894 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Children who are high-risk (ASA III-IV) and whose parents or guardians consent to participate, undergoing anorectal or penile surgeries.

Probably not a fit

Patients without adequate nerve block response or with contraindications to regional anesthesia may not experience benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

The trial examines the use of ultrasound-guided sacral multifidus plane blocks as part of perioperative analgesia for pediatric patients at high anesthetic risk undergoing anorectal or penile procedures. It compares regional anesthesia with standard systemic analgesia to determine if the nerve block reduces reliance on systemic pain medicines and related complications. The approach involves placing local anesthetic in the plane between the sacral multifidus muscle and the intermediate sacral crest on both sides. Outcomes focus on pain control, recovery trajectory, and potential adverse effects in a high-risk pediatric population. The study is conducted at Zagazig University Hospital with parental consent as a key criterion for participation.

Why it matters

Potential benefit: If successful, this approach could improve postoperative pain control while lowering the risks associated with systemic analgesics in high-risk children.

How similar studies have gone: Previous regional anesthesia approaches in pediatric patients have shown pain-reduction benefits in similar contexts, though this exact block and population may be less established.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Parents or caregivers' acceptance.
* High-risk pediatric patients (the American Society of Anesthesiologists physical status class III-IV)
* Body mass index equal to 5%: 85% of the same age and sex.

Exclusion Criteria:

* Child with a contraindication to the regional block, such as infection at the site of injection, or coagulopathy.
* Pre-existing neurological disorders.

Where it's running

  • Zagazig university hospital
    Zagazig, Egypt
    Recruiting

Study contacts

  • Principal investigator: Abdelrazek yousef, MD — Department of Pediatric surgery, Zagazig University
  • Study coordinator: Abdalla Mohamed Goda Mohamed, MD
  • Email: drabdogoda@gmail.com
  • Phone: 1114166085

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.