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Recruiting NCT07610824

NCT07610824 Intraoperative Driving Pressure and Postoperative Lung Ultrasound Score in Robot-Assisted Radical Prostatectomy

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Clinical Trial Summary
NCT ID NCT07610824
Status Recruiting
Phase
Sponsor Ankara Etlik City Hospital
Condition Mechanical Ventilation
Study Type OBSERVATIONAL
Enrollment 76 participants
Start Date 2026-05-30
Primary Completion 2026-08-20

Eligibility & Interventions

Sex Male only
Min Age 18 Years
Max Age 80 Years
Study Type OBSERVATIONAL

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 76 participants in total. It began in 2026-05-30 with a primary completion date of 2026-08-20.

⚠ 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 primary objective of this study is to evaluate the relationship between intraoperative driving pressure and postoperative lung ultrasound scores in patients undergoing robot-assisted laparoscopic radical prostatectomy. During this specific surgery, factors such as pneumoperitoneum and patient positioning can significantly affect respiratory mechanics. Postoperative lung condition will be objectively assessed using the lung ultrasound score (LUS). The findings may provide valuable insights for optimizing intraoperative mechanical ventilation strategies.

Eligibility Criteria

Inclusion Criteria: * Male patients aged between 18 and 80 years. Scheduled for elective robot-assisted laparoscopic radical prostatectomy. American Society of Anesthesiologists (ASA) physical status I, II, or III. Willingness to provide written informed consent. Exclusion Criteria: * Patient refusal to participate. Severe obstructive or restrictive pulmonary disease (e.g., severe COPD, uncontrolled asthma). Body Mass Index (BMI) \> 35 kg/m\^2. Pre-existing severe lung pathology or active pulmonary infection. Hemodynamic instability or severe cardiovascular disease (e.g., severe heart failure, recent myocardial infarction). Requirement for postoperative mechanical ventilation. Emergency surgery.

Contact & Investigator

Central Contact

Fehmi Güralp Güray, MD

✉ guralpguray1995@gmail.com

📞 +905058618969

Frequently Asked Questions

Who can join the NCT07610824 clinical trial?

This trial is open to male participants only, aged 18 Years or older, up to 80 Years, studying Mechanical Ventilation. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07610824 currently recruiting?

Yes, NCT07610824 is actively recruiting participants. Contact the research team at guralpguray1995@gmail.com for enrollment information.

Where is the NCT07610824 trial being conducted?

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

Who is sponsoring the NCT07610824 clinical trial?

NCT07610824 is sponsored by Ankara Etlik City Hospital. The trial plans to enroll 76 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