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Recruiting NCT07020390

NCT07020390 Effect of Anesthesia Techniques on Quality of Recovery Scores in HOLEP Surgery

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Clinical Trial Summary
NCT ID NCT07020390
Status Recruiting
Phase
Sponsor TC Erciyes University
Condition HoLEP
Study Type OBSERVATIONAL
Enrollment 450 participants
Start Date 2025-06-20
Primary Completion 2026-03-15

Eligibility & Interventions

Sex Male only
Min Age 18 Years
Max Age N/A
Study Type OBSERVATIONAL
Interventions
Anesthesia method

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 450 participants in total. It began in 2025-06-20 with a primary completion date of 2026-03-15.

⚠ 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

The aim of this observational study is to evaluate the effects of different anesthesia techniques on the quality of recovery (QoR) and patient satisfaction in male patients, typically older adults with benign prostatic hyperplasia, undergoing Holmium Laser Enucleation of the Prostate (HoLEP). Participants will undergo HoLEP surgery under one of three anesthesia techniques-general, spinal, or combined spinal-epidural anesthesia-and will complete the QoR-40 questionnaire both before and after the surgery.

Eligibility Criteria

Inclusion Criteria: * Patients scheduled for HOLEP surgery due to benign prostatic hyperplasia. * Patients who consent to participate in the study. Exclusion Criteria: * Refusal to participate in the study * Presence of cognitive impairment * Use of psychoactive medications * Failure of the intraoperative anesthesia technique and necessity to change the anesthesia method * Requirement for reoperation or admission to the intensive care unit * Voluntary withdrawal from the study

Contact & Investigator

Central Contact

Gamze Talih

✉ gamzetalih@gmail.com

📞 +905447604780

Frequently Asked Questions

Who can join the NCT07020390 clinical trial?

This trial is open to male participants only, aged 18 Years or older, studying HoLEP. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07020390 currently recruiting?

Yes, NCT07020390 is actively recruiting participants. Contact the research team at gamzetalih@gmail.com for enrollment information.

Where is the NCT07020390 trial being conducted?

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

Who is sponsoring the NCT07020390 clinical trial?

NCT07020390 is sponsored by TC Erciyes University. The trial plans to enroll 450 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: July 2026  ·  Data Methodology