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Completed

NCT Number: NCT03072329

Neurostimulation in Pudendal Nerve Block

The purpose of this study is to check whether the success rate of blind pudendal nerve block in penile surgery can be optimized by the search for a motor response during neurostimulation.

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Key information

Conditions

Penile Surgery

Age range

6 month and older

Sex eligibility

Male

Study type

Interventional

Phase

Not applicable

Primary location

Hôpital d'Enfants Béchir Hamza

Bab Saadoun, Tunis Governorate, 1029, Tunisia

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Children scheduled for elective penile surgery (hypospadias / circumcision)

Non-inclusion Criteria:

  • Association to further peripheral nerve blocks required

Treatment and study plan

Pudendal nerve block

Procedure

Bupivacaine

Drug

Primary outcomes

  1. Nerve block success

    Time frame: 15 minutes

    Nerve block success is defined by the absence of 20% increase in heart rate or systolic blood pressure baseline values

Sponsors and collaborators

Lead sponsor

Hôpital d'enfants Béchir-Hamza

Other

Registry information

Official study title

Neurostimulation in Pudendal Nerve Block: is That Really Necessary?

Important dates

Study start
2016
Primary completion
2017
Study completion
2017
First posted
Mar 7, 2017
Registry last updated
Mar 7, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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