Etomidate Induction in Hysteroscopic Surgery

NCT ID: NCT05520645

Last Updated: 2022-08-30

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

UNKNOWN

Clinical Phase

NA

Total Enrollment

200 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-08-25

Study Completion Date

2023-12-30

Brief Summary

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This study intends to study the optimal dose induced by etomidate in outpatients undergoing painless hysteroscopic surgery. At present, the dosage in the user manual is 0.1-0.3mg/kg. In clinical use, it is found that 0.1mg/kg often fails to achieve sedative effect, and 0.3mg/kg is prone to muscle twitching. Therefore, three groups of doses of 0.15mg/kg, 0.2mg/kg and 0.25mg/kg are set. It is hoped that this study will provide a basis for clinical evaluation of etomidate in anesthesia induction of hysteroscopic surgery.

Detailed Description

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Conditions

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Etomidate Induced Dose Hysteroscopic Surgery

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Caregivers

Study Groups

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Eto 0.15mg/kg

Etomidate 0.15mg/kg for anesthesia induction

Group Type EXPERIMENTAL

etomidate

Intervention Type DRUG

use etomidate for anesthesia induction in hysteroscopic surgery

Eto 0.2mg/kg

Etomidate 0.2mg/kg for anesthesia induction

Group Type EXPERIMENTAL

etomidate

Intervention Type DRUG

use etomidate for anesthesia induction in hysteroscopic surgery

Eto 0.25mg/kg

Etomidate 0.25mg/kg for anesthesia induction

Group Type EXPERIMENTAL

etomidate

Intervention Type DRUG

use etomidate for anesthesia induction in hysteroscopic surgery

Propofol 2mg/kg

propofol 2mg/kg for anesthesia induction

Group Type ACTIVE_COMPARATOR

propofol

Intervention Type DRUG

use propofol for anesthesia induction in hysteroscopic surgery

Interventions

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etomidate

use etomidate for anesthesia induction in hysteroscopic surgery

Intervention Type DRUG

propofol

use propofol for anesthesia induction in hysteroscopic surgery

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

Patients to undergo hysteroscopic surgery

Exclusion Criteria

Hemo-dynamically unstable patients Allergic to egg protein Patients with epilepsy
Minimum Eligible Age

18 Years

Maximum Eligible Age

60 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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Peking University Third Hospital

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Other Identifiers

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89476

Identifier Type: -

Identifier Source: org_study_id

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