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NCT04268511

Caudal Epidural Block Versus Ultrasound-Guided Pudendal Nerve Block for Pediatric Circumcision

Completed Last updated 11 August 2020
What this trial tests

trial testing Caudal epidural block group in Circumcision in 100 participants. Completed in 20 December 2019.

Timeline
1 August 2019
Primary endpoint
1 October 2019
20 December 2019

Quick facts

Lead sponsorProf. Dr. Cemil Tascıoglu Education and Research Hospital Organization
StatusCompleted
Study typeOBSERVATIONAL
Enrollment100
Start date1 August 2019
Primary completion1 October 2019
Estimated completion20 December 2019
Sites1 location across Turkey (Türkiye)

Drugs / interventions tested

Conditions studied

Sponsor

Prof. Dr. Cemil Tascıoglu Education and Research Hospital Organization

Who can join

Adults 4 to 12, any sex, with Circumcision. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The regional anesthesia methods of caudal epidural block (CEB) and dorsal penile nerve block (DPNB) play an important role in providing postoperative pain control in pediatric circumcision surgery. However, the short-term postoperative analgesic effect and the risk of block failure limit the use of DPNB, a peripheral nerve block.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other recruiting trials for Circumcision

Currently open trials in the same condition.

Other Prof. Dr. Cemil Tascıoglu Education and Research Hospital Organization trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04268511.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing