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NCT04840654 · ClinicalTrials.gov registry record · NA
Pudendal vs Caudal Block for Pediatric Penile Surgery
A NA study, sponsored by University of Chicago.
- Terminated
- Registry status
- NA
- Development phase
- 19
- Enrollment target
NCT04840654 is a NA study that was terminated before completion, run by University of Chicago. The registered enrollment target is 19 participants.
The verdict
NCT04840654, a NA study, was terminated before completion, sponsored by University of Chicago.
- TERMINATED
- Registry status
- NA
- Development phase
- 19 participants
- Enrollment target
Study Summary
The study will compare recovery profile in children receiving pudendal blocks vs caudal analgesia for ambulatory circumcision or hypospadias repair in children between 6 months and 2 years. The subjects of the study will be randomized to receive either a caudal or a pudendal block.
Interventions
- PROCEDURE Caudal Block
- PROCEDURE Pudendal Block
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 19 participants |
| Start Date | 2021-05-01 |
| Est. Completion | 2024-10-02 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04840654
The ClinicalTrials.gov registry entry for NCT04840654 describes a study currently listed as terminated, categorized as NA. The registered enrollment target is 19 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Chicago, which has 796 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Caudal Block is the first listed.
NCT04840654 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT04840654 about?
NCT04840654 is a clinical study titled "Pudendal vs Caudal Block for Pediatric Penile Surgery". The study will compare recovery profile in children receiving pudendal blocks vs caudal analgesia for ambulatory circumcision or hypospadias repair in children between 6 months and 2 years. The subjects of the study will be randomized to receive either a caudal or a pudendal block.
What is the current status of trial NCT04840654?
This trial is currently terminated. It is a NA study. The enrollment target is 19 participants. The study started on 2021-05-01. Estimated completion is 2024-10-02.
What interventions are being tested in trial NCT04840654?
The interventions under investigation include: Caudal Block (PROCEDURE), Pudendal Block (PROCEDURE).
Who is sponsoring clinical trial NCT04840654?
This trial is sponsored by University of Chicago, which has 796 total clinical trials registered on ClinicalTrials.gov.
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