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The Effects of Automatic Gas-Controlled Low-Flow Anesthesia on Anesthetic Agent Consumption in Elective Surgeries

NCT ID: NCT06735937

Last Updated: 2024-12-16

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

132 participants

Study Classification

INTERVENTIONAL

Study Start Date

2019-09-01

Study Completion Date

2020-08-31

Brief Summary

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In this study, we aim to compare the effects of end-tidal controlled and manually controlled low-flow anesthesia on anesthetic agent consumption in elective surgeries.

Detailed Description

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In this study, we aim to compare the effects of end-tidal controlled and manually controlled low-flow anesthesia on anesthetic agent consumption in elective surgeries. This evaluation will contribute to understanding whether automated systems provide measurable advantages in clinical settings.This evaluation will contribute to understanding whether automated systems provide measurable advantages in clinical settings.

Conditions

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Low-flow Anesthesia

Keywords

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end-tidal controlled low flow anesthesia consumption

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

OTHER

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

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End-tidal controlled

Patients ventilated using end tidal controlled low-flow anesthesia

Group Type EXPERIMENTAL

Low flow anesthesia

Intervention Type OTHER

Anesthesia management by using low flow anesthesia

Manually controlled

Patients ventilated using manually controlled low flow anesthesia

Group Type EXPERIMENTAL

Low flow anesthesia

Intervention Type OTHER

Anesthesia management by using low flow anesthesia

Interventions

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Low flow anesthesia

Anesthesia management by using low flow anesthesia

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* ASA I-II
* Aged between18-73

Exclusion Criteria

* heart failure
* liver disease
* lung disease
* kidney disease
Minimum Eligible Age

18 Years

Maximum Eligible Age

73 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University of Gaziantep

OTHER

Sponsor Role lead

Responsible Party

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Elzem SEN

Assoc Prof

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Elzem Sen, Assoc Prof

Role: PRINCIPAL_INVESTIGATOR

University of Gaziantep

Locations

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Elzem Sen

Gaziantep, Sehitkamil, Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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2019/355

Identifier Type: -

Identifier Source: org_study_id