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Effect of Erector Spinae Plane Block in Patients Scheduled for Kyphoplasty

NCT05970380 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 61

Last updated 2025-05-06

No results posted yet for this study

Summary

Patients, older than 50 years, with vertebral fracture scheduled for percutaneous balloon kyphoplasty will be enrolled for the study. Some patients will be under local anesthesia with sedation and analgesia for the procedure. Some patients will be performed erector spinae plane block with the guidance of ultrasonography for the procedure. The investigators aim to evaluate the intraoperative and postoperative analgesic requirement of patients. Surgeon's and patients' satisfaction will be also evaluated.

Conditions

  • Erector Spinae Plane Block

Interventions

OTHER

Erector spinae plane block

Local anesthetic solution (40 mL 0.25% bupivacaine totally) will be given bilaterally between the processus transversalis of the fractured vertebra and the erector spinae muscle under ultrasound imaging by an anesthesiologist.

OTHER

Local anesthesia

Local anesthetic solution (20 mL 0.25% bupivacaine) will be given extrapedicular part of the fractured vertebra by the surgeon.

Sponsors & Collaborators

  • Bozyaka Training and Research Hospital

    lead OTHER

Principal Investigators

  • Halide H Şahinkaya, MD · Izmir Bozyaka Training and Research Hospital

  • Alper Tabanlı, MD · Izmir Bozyaka Training and Research Hospital

Eligibility

Min Age
50 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-07-25
Primary Completion
2023-12-30
Completion
2024-02-28

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 NCT05970380 on ClinicalTrials.gov