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Comparison of Minimum Flow and Low Flow Desflurane Anesthesia in Robotic Assisted Laparoscopic Abdominal Surgery

Comparison of Minimum Flow Desflurane Anesthesia With Respiratory Parameters and Blood Gas Analyses and Low Flow Desflurane Anesthesia in Robotic Assisted Laparoscopic Abdominal Surgery

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06520943
Enrollment
70
Registered
2024-07-25
Start date
2024-07-15
Completion date
2024-12-31
Last updated
2024-07-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Minimal Flow Anesthesia, Low Flow Anesthesia, Robotic Assisted Laparoscopic Abdominal Surgery

Brief summary

This study aims to compare the use of low fresh gas flow (1 L/min) desflurane anesthesia with minimum fresh gas flow (0.5 L/min) desflurane anesthesia in patients undergoing robotic-assisted abdominal surgery. The comparison will be based on hemodynamic and respiratory parameters. The secondary aim of our study is to compare the two different fresh gas flow methods in terms of inhalation agent consumption and soda lime consumption.

Interventions

1. Airway pressure (P plateau, Ppeak) values are taken from the anesthesia device data, 2. BIS (from routine BIS monitoring) 3. Temperature (routinely from pharyngeal temperature probe), 4. Oxygen saturation (routinely from the patient monitor) 5. End-tidal CO₂, 6. inspiratory O₂ concentration, 7. Inspiratory CO2 concentration, 8. inspiratory and expiratory desflurane concentrations, 9. tidal volume, 10. MAC is routinely obtained from anesthesia device data. 11. Blood Gas Analysis (COHgb, Ph, PO2, PCO2, SaO2, HCO3, Base deficit, glucose, lactate)

Sponsors

Ankara City Hospital Bilkent
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

* Patients undergoing robotic-assisted abdominal surgery

Exclusion criteria

* serious cardiac, respiratory, hepatic, renal, or mental disorders; * hearing problems; * anxiety, depression, or other psychiatric conditions; * patient's request to leave the study

Design outcomes

Primary

MeasureTime frameDescription
inspiratory O2 concentrationfrom beginning of anesthesia induction to the end of anesthesia (during periopertaive period)inspiratory O2 concentration is measured from anesthesia machine monitor
partial oxygen pressurefrom beginning of anesthesia induction to the end of anesthesia (during periopertaive period)PO2 from blood gas analysis

Secondary

MeasureTime frameDescription
desflurane consumption3th hourdesflurane consumption
changes in liver and kidney function tests from the preoperative values to 48 hours postoperativepostoperative 1st dayto determine the changes in serum aspartate aminotransferase (AST), alanine aminotransferase (ALT), blood urea nitrogen (BUN), and creatinine from the preoperative values to 48 hours postoperative

Countries

Turkey (Türkiye)

Contacts

Primary ContactBetül Güven Aytaç
drbguven@hotmail.com+903125662200

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026