Trials / Completed
CompletedNCT02390388
Pudendal Block Versus Caudal Block for Hypospadias
A Comparison of Effectiveness of Pudendal Nerve Block vs Caudal Block for Hypospadias Surgery in Children
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 80 (actual)
- Sponsor
- Istanbul University · Academic / Other
- Sex
- Male
- Age
- 1 Year – 10 Years
- Healthy volunteers
- Not accepted
Summary
The aim of this prospective randomized study is to assess the analgesic efficacy and duration of Pudendal block compared with Caudal block for pediatric patients undergoing hypospadias surgery concerning intraoperative analgesic and also postoperative total analgesic consumption within 24 hours.
Detailed description
In this prospective study, patients will be randomized into 2 groups, either receiving Caudal Block(CB) or nerve stimulator-guided Pudendal Nerve Block(PNB). Analgesic consumption will be assessed during the first 24 hours postoperatively. The "CHEOPS pain scale" will use to assess postoperative pain.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | pudendal nerve block | nerve stimulator-guided Pudendal block |
| PROCEDURE | caudal block | caudal block |
Timeline
- Start date
- 2014-11-01
- Primary completion
- 2015-05-01
- Completion
- 2015-05-01
- First posted
- 2015-03-17
- Last updated
- 2015-08-26
Source: ClinicalTrials.gov record NCT02390388. Inclusion in this directory is not an endorsement.