Trials / Completed
CompletedNCT03258255
Analgesic Efficiency of Pudendal Nerve Block Versus Penil Block for Circumsion in Children
Comparison of Analgesic Efficiency of Pudendal Nerve Block and Penil Block for Circumsion in Children
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 80 (actual)
- Sponsor
- Istanbul University · Academic / Other
- Sex
- Male
- Age
- 1 Year – 12 Years
- Healthy volunteers
- Accepted
Summary
The aim of this prospective randomized study is to assess the analgesic efficacy of Pudendal block compared with penil block for pediatric patients undergoing circumsion concerning postoperative analgesic consumption within 24 hours.
Detailed description
In this prospective study, patients will be randomized into 2 groups, either receiving penil Block( PNL) 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 | penil or pudendal nerve block in circumcision | regional analgesia methods during the circumsion nerve stimulator guided pudendal block performed by anesthesiologist/ penil block performed by surgeon before circumcision |
Timeline
- Start date
- 2016-11-01
- Primary completion
- 2017-06-01
- Completion
- 2017-07-01
- First posted
- 2017-08-23
- Last updated
- 2017-11-17
Source: ClinicalTrials.gov record NCT03258255. Inclusion in this directory is not an endorsement.