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Search / Trial NCT03914365

Pudendal Nerve Block vs Penile Nerve Block for Analgesia During Pediatric Circumcision

Launched by CHU DE QUEBEC-UNIVERSITE LAVAL · Apr 12, 2019

Trial Information

Current as of July 23, 2025

Unknown status

Keywords

Circumcision Penile Block Pudendal Block Pediatric

ClinConnect Summary

All patients will receive inhalational anaesthesia induction with a mixture of oxygen/nitrous oxide and 6% sevoflurane. Nitrous oxide will be discontinued after loss of consciousness. Standard monitoring will be applied including electrocardiography, pulse oxymetry, capnography and non-invasive blood pressure monitoring. After establishing intravenous access, anaesthesia will be deepened using propofol 1 to 3 mg/kg and fentanyl 1 mcg/kg before laryngeal mask airway insertion or intubation. Neuromuscular blockade will not be administered. Maintenance of anaesthesia will be provided with sevo...

Gender

MALE

Eligibility criteria

  • Inclusion Criteria:
  • Male 1-12 yo undergoing elective circumcision for medical reasons
  • Exclusion Criteria:
  • Allergy to local anaesthetics or medication used in the study Coagulopathy Infection at the injection site Neurologic or neuromuscular disease ASA classification ≥ 4

About Chu De Quebec Universite Laval

CHU de Québec-Université Laval is a leading academic health center in Canada, renowned for its commitment to advancing medical research and improving patient care. As a prominent clinical trial sponsor, it leverages its extensive network of healthcare professionals, researchers, and state-of-the-art facilities to conduct innovative clinical studies across various therapeutic areas. With a strong emphasis on collaboration and ethical standards, CHU de Québec-Université Laval aims to translate scientific discoveries into effective treatments, enhancing health outcomes for diverse populations.

Locations

Québec, , Canada

Patients applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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