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Recruiting NCT06482983

NCT06482983 The Effects of VC Versus PC Ventilation on Cerebral and Respiratory Parameters in Patients Undergoing Laparoscopic Gynecologic Surgery

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Clinical Trial Summary
NCT ID NCT06482983
Status Recruiting
Phase
Sponsor Umraniye Education and Research Hospital
Condition Anesthesia
Study Type INTERVENTIONAL
Enrollment 120 participants
Start Date 2023-05-01
Primary Completion 2024-09-30

Eligibility & Interventions

Sex Female only
Min Age 18 Years
Max Age 70 Years
Study Type INTERVENTIONAL
Interventions
Mechanical Ventilation Mode

Eligibility Fast-Check

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

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 120 participants in total. It began in 2023-05-01 with a primary completion date of 2024-09-30.

⚠ 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 the study was to determine whether the use of different mechanical ventilation modes in patients with Trendelenburg position and CO2 insufflation affects respiration and cerebral oxygenation due to postoperative atelectasis, and was to determine whether there was any hemodynamic effect.

Eligibility Criteria

Inclusion Criteria: * 18-70 age * ASA 1-3 Exclusion Criteria: * Under 18 years of age, over 70 years of age, * ASA IV, * history of severe chronic obstructive pulmonary disease (COPD, GOLD III or IV) ,-history of severe or uncontrolled bronchial asthma, presence of restrictive lung disease, * history of any thoracic surgery operation, need for thoracic drainage before surgery * patients receiving preoperative renal replacement therapy, * congestive heart failure (NYHA grade III or IV), * extremely obese (body Mass Index, BMI \> 35 Kg/m2) * patients without patient consent

Frequently Asked Questions

Who can join the NCT06482983 clinical trial?

This trial is open to female participants only, aged 18 Years or older, up to 70 Years, studying Anesthesia. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06482983 currently recruiting?

Yes, NCT06482983 is actively recruiting participants. Visit ClinicalTrials.gov or contact Umraniye Education and Research Hospital to inquire about joining.

Where is the NCT06482983 trial being conducted?

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

Who is sponsoring the NCT06482983 clinical trial?

NCT06482983 is sponsored by Umraniye Education and Research Hospital. The trial plans to enroll 120 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