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NCT07262073Active, not recruiting

Comparison of Peak Expiratory Flow Changes After Robot-Assisted Versus Open Radical Prostatectomy

Prospective Randomized Controlled Study Comparing Peak Expiratory Flow (PEF) Changes After Robot-Assisted and Open Radical Prostatectomy

Source: ClinicalTrials.gov · Last updated 3 Dec 2025

Brief summary (registry, in English)

This prospective, randomized controlled trial aims to compare perioperative respiratory changes in patients undergoing robot-assisted laparoscopic radical prostatectomy (RALRP) and open radical prostatectomy (ORP). The primary outcome is the change in peak expiratory flow (PEF) from the preoperative period to the early postoperative (2nd hour) period. Secondary outcomes include PEF recovery at 24 hours, and correlations between PEF change and intraoperative factors such as Trendelenburg angle, pneumoperitoneum duration, and ventilatory parameters.

Status (registry)
Active, not recruiting
Study type
Interventional
Enrollment
60 (estimated)
First submitted
23 Nov 2025
Start date
1 Nov 2025
Primary completion date
30 Dec 2025
Lead sponsor
Ankara City Hospital Bilkent
NCT number
NCT07262073

What you commit to

  • Study type: Interventional
  • Planned participants: 60
  • From 1 Nov 2025 to the primary completion date, 30 Dec 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Emergency surgery

Other illness

  • Active upper respiratory tract infection
  • Cognitive impairment preventing participation

Other

  • Moderate/severe COPD (GOLD II-IV)
  • Severe OSA requiring CPAP
  • Inability to perform standardized PEF maneuver

Who the study is looking for

  • Male, 18-80 years old
  • ASA physical status I-III
  • Scheduled for open or robot-assisted radical prostatectomy
  • Able to provide informed consent and follow Turkish instructions

Age in the registry: 18 years to 80 years · Sex: Male · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Ankara Bilkent City Hospital, Department of Anesthesiology
Coordinator of this site? Confirm its status
AnkaraTurkey (Türkiye)Unknown status

This page is information, not medical advice. Discuss any trial with your doctor.