Trials / Unknown
UnknownNCT03046290
Pudendal Block Versus Penian Block For Circumcision In Children
Pudendal Block Versus Penian Block For Circumcision In Children: A Double Blind Randomised Controlled Trial
- Status
- Unknown
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 60 (estimated)
- Sponsor
- Université Libre de Bruxelles · Academic / Other
- Sex
- Male
- Age
- 1 Year – 5 Years
- Healthy volunteers
- Not accepted
Summary
The authors study the efficacy of the pudendal versus penile block for the relief of postoperative pain in children receiving ambulatory circumcision. In this prospective, double-blind, randomized, parallel-arm trial, 60 children recruited during the anesthesia consultation will be allocated a general anesthesia with a pudendal block (PUD group) or a penile block (PEN group). Each block will be made with equal parts lidocaine 1% and ropivacaine 0.75% (0.3 ml/kg).
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | circumcision | |
| DRUG | Lidocaine | |
| DRUG | Ropivacaine |
Timeline
- Start date
- 2017-01-01
- Primary completion
- 2017-04-01
- Completion
- 2017-04-01
- First posted
- 2017-02-08
- Last updated
- 2017-02-08
Locations
1 site across 1 country: Belgium
Source: ClinicalTrials.gov record NCT03046290. Inclusion in this directory is not an endorsement.