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Recruiting NCT07550738

NCT07550738 Effect of Pressure-Controlled Volume Guaranteed Versus Volume-Controlled Ventilation Modes on Hemodynamic Outcomes e.g ( SV, CO ) and Respiratory Mechanics During Laparoscopic Abdominal Cancer Surgeries With Exaggerated Trendelenberg Postion

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Clinical Trial Summary
NCT ID NCT07550738
Status Recruiting
Phase
Sponsor Assiut University
Condition PCV-VG Versus VCV Ventilation Mode Effects on Hemodynamics
Study Type INTERVENTIONAL
Enrollment 60 participants
Start Date 2026-04-01
Primary Completion 2027-06

Eligibility & Interventions

Sex All sexes
Min Age 20 Years
Max Age 80 Years
Study Type INTERVENTIONAL
Interventions
electrical cardiometry ('ICON CARDIOTRONIC, OSYPKA MEDICAL') , Lung ultrasonography (LUS) for atelectasis

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 60 participants in total. It began in 2026-04-01 with a primary completion date of 2027-06.

⚠ 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 outcome is to compare the hemodynamic outcomes ( e.g SV , CO and CI ) using The ICON of two different modes of ventilation ( VCV and PC-VG ) during laparoscopic abdominal cancer surgeries with exaggerated trendelenburg position. And the secondary outcomes is to compare the respiratory effects ( e.g atelectasis development , plateau pressure(Pplat) , peak inspiratory pressure(PIP) , dyn. compliance and postoperative inflammatory indicators e.g CRP and WBCs ) of two different modes of ventilation ( VCV and PC-VG ) during laparoscopic abdominal cancer surgeries with exaggerated trendelenburg position.

Eligibility Criteria

Inclusion Criteria: 1 - All patients who will be scheduled for elective laparoscopic abdominal cancer surgeries 2- patients aged 20-80 years 3- patients have an American Society of Anesthesiologists (ASA) physical status I-II Exclusion Criteria: 1 - Patients with severe systemic disease (history of myocardial infarction, chronic obstructive, or restrictive lung disease) 2- Obese patients (BMI \> 30) 3- patients with neurologic or neuromuscular diseases.

Contact & Investigator

Central Contact

Saif eldeen Gamal Khalaf, Assistant lecturer

✉ saifeldeen616@gmail.com

📞 +20-1033893202

Frequently Asked Questions

Who can join the NCT07550738 clinical trial?

This trial is open to participants of all sexes, aged 20 Years or older, up to 80 Years, studying PCV-VG Versus VCV Ventilation Mode Effects on Hemodynamics. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07550738 currently recruiting?

Yes, NCT07550738 is actively recruiting participants. Contact the research team at saifeldeen616@gmail.com for enrollment information.

Where is the NCT07550738 trial being conducted?

This trial is being conducted at Asyut, Egypt.

Who is sponsoring the NCT07550738 clinical trial?

NCT07550738 is sponsored by Assiut University. The trial plans to enroll 60 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