Actively Recruiting

Phase Not Applicable
Age: 18Years - 87Years
All Genders
ID07304479

Effects of Sevoflurane Versus Desflurane Anesthesia Under Protective Mechanical Ventilation for Robotic Assisted Surgery on Airway Plateau Pressure: a Randomized, Prospective, Blinded Pilot Study

Led by National and Kapodistrian University of Athens · Updated on 2025-12-26

50

Participants Needed

1

Research Sites

4 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating the effects of two inhalational anesthetics, sevoflurane and desflurane, during robotic-assisted abdominal surgery. The study focuses on how these anesthetics influence lung mechanics, particularly airway plateau pressure, under protective mechanical ventilation. This comparison is important because inhalational anesthetics may offer lung protection and reduce inflammation during surgery, yet little is known about their differences in this surgical setting. Participants will receive either sevoflurane or desflurane anesthesia while undergoing elective robotic-assisted abdominal surgery. Both anesthetics are volatile agents administered during the procedure, with patients randomly assigned to one of these two treatment groups. The study is conducted as a randomized, prospective, and triple-blinded pilot trial to carefully assess the effects of each anesthetic. During the surgery, researchers will monitor airway plateau pressure to understand lung mechanics under each anesthetic. Patient evaluations include perioperative measurements related to respiratory function. The trial spans from the preparation before surgery through the procedure itself, with safety and lung function outcomes assessed during this time. Participants will be followed until the completion of their surgical and immediate postoperative period to collect relevant data.

CONDITIONS

Brief Title

Effects of Sevoflurane Versus Desflurane Anesthesia Under Protective Mechanical Ventilation for Robotic Assisted Surgery

Who Can Participate

Age: 18Years - 87Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 to 87 years
  • Undergoing elective robotic-assisted abdominal surgery
  • ASA physical status I-III
Not Eligible

You will not qualify if you...

  • ASA physical status IV or V
  • Emergency surgery
  • Renal insufficiency
  • Clinically significant respiratory disease
  • Cardiomyopathy
  • Uncontrolled hypertension

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Treatment

Duration - During surgery

Participants receive either Sevoflurane or Desflurane anesthesia during robotic assisted laparoscopic surgery under protective mechanical ventilation.

1 surgery visit (in-person)

Trial Site Locations

Total: 1 location

1

Aretaieion University Hospital

Athens, Greece, 11528

Actively Recruiting

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Research Team

A

Aliki Tympa, MD,PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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Published Research Related To This Trial

Total intravenous anaesthesia versus inhalational anaesthesia for adults undergoing transabdominal robotic assisted laparoscopic surgery.

Suzanne Forsyth Herling, Bjørn Dreijer, Gitte Wrist Lam...

https://pubmed.ncbi.nlm.nih.gov/28374886