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Caudal Block Versus Local Wound Infiltration for Inguinal Procedures

U

University Hospital Tuebingen

Status

Completed

Conditions

Anesthesia, Caudal

Study type

Observational

Funder types

Other

Identifiers

NCT04590027
621/2013BO1

Details and patient eligibility

About

Single-centre observational study to analyse whether there is a difference in post-operative pain scores and set up time when comparing caudal block with local wound infiltration

Full description

Inguinal procedures in children are surgical frequently performed in an outpatient setting. This study analyzed regional analgesia for inguinal procedures in toddlers comparing caudal block with local wound infiltration and assessed post-operative pain scores as well as process times.A number of documents were compiled to inform and record data: a standard anaesthesia protocol, a documentation sheet for intraoperative recording, an information leaflet for the parents and a documentation sheet for the post-operative course of 24 hours .

Caudal anaesthesia was performed after induction of anaesthesia. In patients getting wound infiltration ropivacaine 0.375% 0.5 ml kg-1 was injected subcutaneously after closing of the fascia transversalis.

Parents were informed about the study and invited to participate upon arriving on the outpatient ward if the patient fulfilled the following inclusion criteria: scheduled for elective inguinal procedure, age three to 72 months, no contraindication for either local or caudal analgesia, no comorbidities. If parents agreed to participate, written informed consent was obtained. Pain score and administration of analgesics, vomiting, interval until micturition and interval until mobilization as well as sleep quality during the first post-operative night were documented by the parents in the provided booklet.

Enrollment

86 patients

Sex

All

Ages

3 to 68 months old

Volunteers

No Healthy Volunteers

Inclusion criteria

Exclusion criteria

  • no return of questionnaire
  • parents do not understand language

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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