- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06430593
Evaluation of Low Flow and Normal Flow Anesthesia Management in Robotic Assisted Laparoscopic Surgeries
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.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Robotic surgery is the performance of laparoscopic surgery using a robotic interface. The robotic surgery system used today is called Da Vinci S. In surgeries performed with the help of a robot, the surgeon can work more precisely and with greater maneuverability. Therefore, an operation can be performed that is less traumatic for the patient than other methods.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 these applications, fresh gas flow in anesthesia systems can be made with traditional high, normal or low flow strategies, depending on the preference of the clinicians.Low-flow anesthesia creates a breathing air closer to physiological conditions during anesthesia by heating and humidifying the inhaled gases. In addition, it provides cost advantage by reducing inhalation agent consumption and reduces atmospheric pollution. It is suggested that the use of both fresh gas flow amounts does not pose a safety risk for patients, and that the use of low-flow anesthesia methods should be more widespread due to the advantages it provides. In our clinic, investigators 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.
Study Type
Enrollment (Estimated)
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Ages 18-75
- ASA I,II
- Patients undergoing robotic-assisted laparoscopic surgery
Exclusion Criteria:
- 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
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
low-flow anesthesia
0,5 lt/min
|
0,5 l/min >1 l/min
Other Names:
|
|
normal flow anesthesia
>1 lt/min
|
0,5 l/min >1 l/min
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Hemodynamic Parameters
Time Frame: Perioperative period(approximately 3-6 hours)
|
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
Time Frame: Perioperative period(approximately 3-6 hours)
|
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
Time Frame: Perioperative period(approximately 3-6 hours)
|
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
Time Frame: Perioperative period(approximately 3-6 hours)
|
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
Time Frame: Perioperative period(approximately 3-6 hours)
|
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
Time Frame: Perioperative period(approximately 3-6 hours)
|
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)
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2024- 183
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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