RecruitingInterventionalNot ApplicableUpdated Jun 17, 2025
A Comparison Between Propofol and Etomidate in Hysteroscopy on Effect of Postoperative Sedation and Cognitive Function in Elderly Patients | NCT02147678 | Trialant
Unknown statusInterventionalPhase 4Updated May 28, 2014
A Comparison Between Propofol and Etomidate in Hysteroscopy on Effect of Postoperative Sedation and Cognitive Function in Elderly Patients
ClinicalTrials.gov ID
NCT02147678
Lead Sponsor
Shaanxi Provincial People's HospitalOTHER
Overall Status
Unknown status
Study Type
Interventional
Phase
Phase 4
Enrollment
120Estimated
Last Update Posted
May 28, 2014Estimated
Start Date
Dec 2014
Primary Completion Date
Feb 2015Estimated
Completion Date
Feb 2015Estimated
Brief Summary
To compare the effect of propofol and etomidate in hysteroscopy on postoperative sedation and cognitive function in elderly patients
Hysteroscopy
Hemodynamics
Sedation
Etomidate
Propofol
Remifentanil
Anesthesia induction
Ages Eligible for Study
Adult (18-64)Older Adult (65+)
Sexes Eligible for Study
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Aged between 60 and 80 years
Selective hysteroscopic operation
American Society of Anesthesiology (ASA) Physical Status: Ⅰ or Ⅱ
Signed informed consent form
Expected operation duration is within 60 minutes
Exclusion Criteria:
Serious cardiac, cerebral, liver, kidney, lung, endocrine disease or sepsis
Long use of hormone or history of adrenal suppression
Allergy to trial drug or other contraindication
History or expected difficult airway
Identified, suspected abuse or long use of narcotic analgesia