Evaluation of Low Flow and Normal Flow Anesthesia Management in Robotic Assisted Laparoscopic Surgeries
1 other identifier
observational
68
0 countries
N/A
Brief Summary
Robotic-assisted laparoscopic surgery has many advantages compared to conventional open surgery, such as less postoperative pain, shorter hospital stays, and faster recovery times. Robot-assisted surgeries require general anesthesia. In our clinic, we routinely apply low-flow anesthesia methods in addition to normal flow methods in many surgical applications, according to clinician preferences. The aim of this study is to determine the effects of low flow (0.5 lt/min) and normal flow (\>1 lt/min) anesthesia applications in robotic-assisted laparoscopic surgeries. To compare perioperative hemodynamic and respiratory parameters in terms of inhalation agent and soda lime consumption.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Aug 2024
Shorter than P25 for all trials
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
May 14, 2024
CompletedFirst Posted
Study publicly available on registry
May 28, 2024
CompletedStudy Start
First participant enrolled
August 20, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 20, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
January 20, 2025
CompletedAugust 13, 2024
May 1, 2024
5 months
May 14, 2024
August 11, 2024
Conditions
Keywords
Outcome Measures
Primary Outcomes (6)
Hemodynamic Parameters
It was aimed to compare heart rates in patients undergoing low flow (0.5 lt/min) and normal flow (\>1 lt/min) anesthesia.
Perioperative period(approximately 3-6 hours)
Hemodynamic Parameters
It was aimed to compare blood pressure in patients undergoing low flow (0.5 lt/min) and normal flow (\>1 lt/min) anesthesia.
Perioperative period(approximately 3-6 hours)
Respiratory parameters
It was aimed to compare oxygen saturation in patients undergoing low flow (0.5 lt/min) and normal flow (\>1 lt/min) anesthesia.
Perioperative period(approximately 3-6 hours)
Respiratory parameters
It was aimed to compare endtidal carbon dioxide in patients undergoing low flow (0.5 lt/min) and normal flow (\>1 lt/min) anesthesia.
Perioperative period(approximately 3-6 hours)
Inhalation agent (sevoflurane) consumption
It was aimed to compare inhalation agent (sevoflurane) consumption (lt) in patients undergoing low flow (0.5 lt/min) and normal flow (\>1 lt/min) anesthesia.
Perioperative period(approximately 3-6 hours)
Soda lime consumption
It was aimed to compare soda lime consumption in patients undergoing low flow (0.5 lt/min) and normal flow (\>1 lt/min) anesthesia. Soda lime consumption refers to the number of changes of the soda lime canister.
Perioperative period(approximately 3-6 hours)
Study Arms (2)
low-flow anesthesia
0,5 lt/min
normal flow anesthesia
\>1 lt/min
Interventions
0,5 l/min \>1 l/min
Eligibility Criteria
Ages 18-75, ASA I,II, Patients undergoing robotic-assisted laparoscopic surgery
You may qualify if:
- Ages 18-75
- ASA I,II
- Patients undergoing robotic-assisted laparoscopic surgery
You may not qualify if:
- ASA III,IV,V
- Those with serious cardiac, respiratory, hepatic, renal disease
- People with mental status disorders, psychiatric illnesses
- Patients with hearing problems and glaucoma
- Desire to be out of work
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Conditions
Study Design
- Study Type
- observational
- Observational Model
- CASE ONLY
- Time Perspective
- PROSPECTIVE
- Target Duration
- 6 Months
- Sponsor Type
- OTHER GOV
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Anesthesiologist
Study Record Dates
First Submitted
May 14, 2024
First Posted
May 28, 2024
Study Start
August 20, 2024
Primary Completion
January 20, 2025
Study Completion
January 20, 2025
Last Updated
August 13, 2024
Record last verified: 2024-05