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Pudendal Block Versus Penian Block For Circumcision In Children

U

Université Libre de Bruxelles

Status

Unknown

Conditions

Postoperative Pain
Circumcision
Regional Anesthesia

Treatments

Procedure: circumcision
Drug: Lidocaine
Drug: Ropivacaine

Study type

Interventional

Funder types

Other

Identifiers

NCT03046290
U1111-1191-4760 (Other Identifier)
B406201630517

Details and patient eligibility

About

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).

Enrollment

60 estimated patients

Sex

Male

Ages

1 to 5 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • circumcision in day surgery hospital

Exclusion criteria

  • allergy to amino-amide local anesthetics
  • parental consent not received
  • infection at injection site

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

60 participants in 2 patient groups

Pudendal Block
Active Comparator group
Description:
The anesthesia is produced by blocking the pudendal nerves near the ischial spine of the pelvis.Local anesthetic (mixed of ropivacaine and lidocaine) is injected into the pudendal canal where the pudendal nerve is located.
Treatment:
Drug: Lidocaine
Procedure: circumcision
Drug: Ropivacaine
Penian Block
Active Comparator group
Description:
The anesthesia is produced by blocking the dorsal penile nerves. Local anesthetic (mixed of ropivacaine and lidocaine)is injected under the pubis symphysis just below the Buck fascia where the nerve is located.
Treatment:
Drug: Lidocaine
Procedure: circumcision
Drug: Ropivacaine

Trial contacts and locations

1

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Central trial contact

John Nicolardot; John Nicolardot, MD

Data sourced from clinicaltrials.gov

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