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Recruiting NCT07578545

NCT07578545 The Impact of Video-assisted Thoracic Surgery and Regional Anaesthesia on Postoperative Opioid Consumption and Pain Scores

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Clinical Trial Summary
NCT ID NCT07578545
Status Recruiting
Phase
Sponsor Antalya Training and Research Hospital
Condition Thoracic Surgery
Study Type OBSERVATIONAL
Enrollment 96 participants
Start Date 2026-05-04
Primary Completion 2026-10-04

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 75 Years
Study Type OBSERVATIONAL
Interventions
Paravertebral block groupİntertransverse process block groupErector spinae plane block group

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 96 participants in total. It began in 2026-05-04 with a primary completion date of 2026-10-04.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief 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.

Eligibility Criteria

Inclusion Criteria: * aged 18-75 years * American Society of Anaesthesiology (ASA) score I-III * body mass index (BMI) \<35kg/m2 * scheduled for elective VATS Exclusion Criteria: * ASA score ≥4 * BMI ≥35 kg/m2 * declining to give written informed consent * controendications for block application * inability to undergo block application * history neurological disease or peripheral nerve disease * history of chronic opioid use * history of severe liver or kidney failure * patients admitted to the intensive care unit postoperatively intubated

Contact & Investigator

Central Contact

Sadik Ozmen

✉ sadikozmen@hotmail.com

📞 +905324205282

Principal Investigator

Sadik Ozmen

PRINCIPAL INVESTIGATOR

University of Health Sciences, Antalya Training and Research Hospital

Frequently Asked Questions

Who can join the NCT07578545 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 75 Years, studying Thoracic Surgery. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07578545 currently recruiting?

Yes, NCT07578545 is actively recruiting participants. Contact the research team at sadikozmen@hotmail.com for enrollment information.

Where is the NCT07578545 trial being conducted?

This trial is being conducted at Antalya, Turkey (Türkiye).

Who is sponsoring the NCT07578545 clinical trial?

NCT07578545 is sponsored by Antalya Training and Research Hospital. The principal investigator is Sadik Ozmen at University of Health Sciences, Antalya Training and Research Hospital. The trial plans to enroll 96 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology