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Clinical Trial Summary

The study was done to evaluate the effects of the follicular and luteal phases of the menstrual cycle on sedation level at loss of consciousness and bispectral index reach to 50 during propofol anesthesia, in patients with and without preoperative intravenous dexmedetomidine .


Clinical Trial Description

n/a


Study Design

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Prevention


Related Conditions & MeSH terms


NCT number NCT02035930
Study type Interventional
Source Fudan University
Contact
Status Completed
Phase Phase 4
Start date November 2010
Completion date November 2012

See also
  Status Clinical Trial Phase
Recruiting NCT01483365 - The Need for Luteal Support in NC-FET Phase 0