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Erector Spinae Plane Block for Children Undergoing Thoracoscopic Sympathectomy

NCT06984874 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2025-05-22

No results posted yet for this study

Summary

This study aims to evaluate the influence of ultrasound-guided erector spinae plane block on postoperative pain and diaphragmatic dysfunction in pediatric patients undergoing thoracoscopic sympathectomy.

Conditions

  • Erector Spinae Plane Block
  • Children
  • Thoracoscopic Sympathectomy

Interventions

OTHER

Erector spinae plane block

Patients will receive bilateral erector spinae plane block after the induction of general anesthesia as a study group.

OTHER

General anesthesia

Patients will not receive the block after the induction of general anesthesia as a control group.

Sponsors & Collaborators

  • Menoufia University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
6 Years
Max Age
16 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-01-15
Primary Completion
2025-12-01
Completion
2025-12-01

Countries

  • Egypt

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 NCT06984874 on ClinicalTrials.gov