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Recruiting NCT07304479

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

No phase Interventional Respiratory Mechanics Intraoperative

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Sevoflurane (Volatile Anesthetic), Desflurane (volatile anesthetic).
Who it may be relevant to
Registry conditions: Respiratory Mechanics, Intraoperative. Basic parameters: 18 years — 87 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Greece
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

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

Overview

Inhalational anesthetics, when used in abdominal surgery, offer advantages of lung protection and reduced alveolar inflammation. There is little literature, however, in the comparative use of sevoflurane versus desflurane anesthesia in patients undergoing abdominal robotic-assisted surgery and their effects on lung mechanics.

Interventions

  • Drug Sevoflurane (Volatile Anesthetic)
    Sevoflurane for robotic assisted laparoscopic surgery
  • Drug Desflurane (volatile anesthetic)
    Desflurane for robotic assisted laparoscopic surgery

Primary outcome measures

  • airway plateau pressure [Time frame: Perioperatively]

Eligibility criteria

Inclusion criteria

  • Age 18 to 87 years
  • Undergoing elective robotic-assisted abdominal surgery
  • ASA physical status I-III

Exclusion criteria

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

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Triple blind
Primary purpose
Prevention

Study locations

Greece · 1 center
  • Aretaieion University Hospital — Athens

Publications

  • Herling SF, Dreijer B, Wrist Lam G, Thomsen T, Moller AM. Total intravenous anaesthesia versus inhalational anaesthesia for adults undergoing transabdominal robotic assisted laparoscopic surgery. Cochrane Database Syst Rev. 2017 Apr 4;4(4):CD011387. doi: 10.1002/14651858.CD011387.pub2. PMID 28374886

Identifiers

NCT: NCT07304479 · 705/25-07-2025

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗