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The analgesic efficacy of ultrasound guided Pudendal nerve block versus sacral erector spinae plane block for children underdoing hypospadias surgery: A double blinded, randomized controlled study

The analgesic efficacy of ultrasound guided Pudendal nerve block versus sacral erector spinae plane block for children underdoing hypospadias surgery: A double blinded, randomized controlled study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
PACTR
Registry ID
PACTR202505717978875
Enrollment
64
Registered
2025-05-06
Start date
2025-05-03
Completion date
Unknown
Last updated
2026-09-14

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

Conditions

Paediatrics Anaesthesia

Interventions

PNB group
Sacral ESPB group

Sponsors

Mansoura university children hospital
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: ASA status I or II patients, of age 3 to 10 years. Scheduled for hypospadias surgery that needed hospital stay for at least 1 day in pediatric surgery department at Mansoura university children hospital.

Exclusion criteria

Exclusion criteria: 1. Patient with history of growth retardation or mental disorders affecting pain score assessment. 2. patient’s parents refuse. 3. Hematological diseases, bleeding or coagulation abnormality. 4. Sepsis and local skin infection at site of the block. 5. Known hypersensitivity to the study drugs. 6. Patients underneath or over the age. 7. Patients with vertebral column abnormalities or any neurological disorders. 8. Psychiatric diseases.

Design outcomes

Primary

MeasureTime frame
the time to first rescue analgesia in children undergoing hypospadias repair with US guided sacral ESPB or US guided pudendal nerve block.

Secondary

MeasureTime frame
• Compare intraoperative hemodynamic parameters (heart rate, systolic and diastolic blood pressure), fentanyl consumption ; postoperative face, leg, activity, cry, controllability (FLACC) score and analgesic consumption in 24 h. Consumption of paracetamol will be assessed during the first 24 h postoperatively.

Countries

Egypt

Contacts

Public ContactAhmed Alaidy

lecturer of anesthesia and surgical ICU at Mansoura faculty of medicine Egypt

a_m_elaidy88@yahoo.com0201099719913

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Sep 19, 2026