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The Impact of Video-assisted Thoracic Surgery and Regional Anaesthesia on Postoperative Opioid Consumption and Pain Scores

NCT07578545 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 96

Last updated 2026-05-11

No results posted yet for this study

Summary

This present study aims is to compare the effects of ultrasound-guided paravertebral block, intertransverse process block, and erector spinae plane block on postoperative opioid consumption, and pain scores in patients undergoing VATS.

Conditions

  • Thoracic Surgery
  • Videoassisted Thoracoscopic Surgery,One-lung Ventilation
  • Regional Anaesthesia
  • Postoperative Analgesia
  • Pain Score

Interventions

OTHER

Paravertebral block group

Before the surgery, ultrasoud-guided paravertebral block will be performed before the surgery under standart anaesthesia monitoring

OTHER

İntertransverse process block group

Before the surgery, ultrasoud-guided intertransverse process block will be performed before the surgery under standart anaesthesia monitoring

OTHER

Erector spinae plane block group

Before the surgery, ultrasoud-guided erector spinae plane block will be performed before the surgery under standart anaesthesia monitoring

Sponsors & Collaborators

  • Antalya Training and Research Hospital

    lead OTHER_GOV

Principal Investigators

  • Sadik Ozmen · University of Health Sciences, Antalya Training and Research Hospital

  • Batuhan Kılıc · University of Health Sciences, Antalya Training and Research Hospital

  • Hacer Boztepe Yesilcay · University of Health Sciences, Antalya Training and Research Hospital

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-05-04
Primary Completion
2026-10-04
Completion
2026-11-04

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 NCT07578545 on ClinicalTrials.gov