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Sacral Erector Spinae Plane Blocks in Pediatric Patients

NCT05415046 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 15

Last updated 2022-08-17

No results posted yet for this study

Summary

Patients who were operated by Department of Pediatric Surgery and who received sacral erector spinae plane blocks as a part of postoperative analgesia management will be scanned.

Conditions

  • Postoperative Pain

Interventions

PROCEDURE

Sacral ESPB

Erector spinae plane block performed with 0,25% bupivacaine (1 mL/kg-max 20mL), under general anesthesia before the start of the surgery.

Sponsors & Collaborators

  • Kocaeli University

    lead OTHER

Eligibility

Min Age
1 Month
Max Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-06-15
Primary Completion
2022-07-07
Completion
2022-07-08

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05415046 on ClinicalTrials.gov