NCT06430593

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

35
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
68

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Aug 2024

Shorter than P25 for all trials

Status
not yet recruiting

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

Completed
14 days until next milestone

First Posted

Study publicly available on registry

May 28, 2024

Completed
3 months until next milestone

Study Start

First participant enrolled

August 20, 2024

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 20, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

January 20, 2025

Completed
Last Updated

August 13, 2024

Status Verified

May 1, 2024

Enrollment Period

5 months

First QC Date

May 14, 2024

Last Update Submit

August 11, 2024

Conditions

Keywords

low-flow anesthesiarobotic-assisted surgerygeneral anesthesia

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

Procedure: low-flow anesthesia

normal flow anesthesia

\>1 lt/min

Procedure: low-flow anesthesia

Interventions

0,5 l/min \>1 l/min

Also known as: normal flow anesthesia
low-flow anesthesianormal flow anesthesia

Eligibility Criteria

Age18 Years - 75 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

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

Neoplasms

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