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NCT05520645

Etomidate Induction in Hysteroscopic Surgery

Status unknown NA Last updated 30 August 2022
What this trial tests

NA trial testing etomidate in Etomidate Induced Dose in 200 participants. Status unknown.

Timeline
25 August 2022
Primary endpoint
30 September 2023
30 December 2023

Quick facts

Lead sponsorPeking University Third Hospital
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposetreatment
Enrollment200
Start date25 August 2022
Primary completion30 September 2023
Estimated completion30 December 2023

Drugs / interventions tested

Conditions studied

Sponsor

Peking University Third Hospital

Who can join

Adults 18 to 60, female only, with Etomidate Induced Dose or Hysteroscopic Surgery. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of etomidate

Trials testing the same drug.

Other Peking University Third Hospital trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05520645.

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