Not Yet RecruitingNot Applicable

Analgesia in Pediatric Hypospadias Surgeries

26 participantsStarted 2024-05

Plain-language summary

The primary aim of the current study will be to use the duration until the first postoperative analgesic requirement after two different block techniques to compare the analgesic effect. The secondary aims will be to compare the two methods for postoperative Children's Hospital Eastern Ontario Pain Scale (CHEOPS) scores, complications and parental satisfaction scores.

Who can participate

Age range1 Year – 7 Years

SexMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * • Children aged 1-7 years old * ASA I and II * Children scheduled for primary hypospadias repair Exclusion Criteria: * • Patient's guardian refusal to participate in the study. * Children with Behavioural changes; physical or developmental delay; neurological disorder or psychological disorder. * Children on sedative or anticonvulsant medication. * Bleeding diathesis * Infection of injecting area * significant organ dysfunction, cardiac, liver or mental retardation. * Congenital low back anomaly. * Known allergy to the study drugs

What they're measuring

postoperative pain and analgesic requirement after two different block techniques to compare the analgesic effect.

Timeframe: 24 hours after the end of surgery

Trial details

NCT IDNCT06410482

SponsorAssiut University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2025-05

Contact for this trial

Esraa Gaafer, Resident

+201156063201 esraa.gaafer10@gmail.com

View on ClinicalTrials.gov More Hypospadias trials