Clinical Trials Directory

Trials / Unknown

UnknownNCT05520645

Etomidate Induction in Hysteroscopic Surgery

Randomized Controlled Study of Etomidate Induction in Hysteroscopic Surgery

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
200 (estimated)
Sponsor
Peking University Third Hospital · Academic / Other
Sex
Female
Age
18 Years – 60 Years
Healthy volunteers
Accepted

Summary

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.

Conditions

Interventions

TypeNameDescription
DRUGetomidateuse etomidate for anesthesia induction in hysteroscopic surgery
DRUGpropofoluse propofol for anesthesia induction in hysteroscopic surgery

Timeline

Start date
2022-08-25
Primary completion
2023-09-30
Completion
2023-12-30
First posted
2022-08-30
Last updated
2022-08-30

Source: ClinicalTrials.gov record NCT05520645. Inclusion in this directory is not an endorsement.