Status:
TERMINATED
Comparison of Two Different Sedation Protocols During Transvaginal Oocyte Retrieval
Lead Sponsor:
Attikon Hospital
Conditions:
Infertility
Eligibility:
FEMALE
25-45 years
Brief Summary
The effects of two different sedation protocols during transvaginal oocyte retrieval will be investigated on propofol consumption as a rescue sedative and on IVF success. One group will receive dexmed...
Detailed Description
Women will be consecutively allocated into one of the following two groups using a 1:1 ratio in order to avoid any potential source of bias. Group DEX: women will receive dexmedetomidine (solution 4 ...
Eligibility Criteria
Inclusion
- female patients between 25 and 45 years old that do not meet any of the exclusion criteria
Exclusion
- patient refusal, epilepsy, GERD, morbid obesity, drug allergy, ASA class \>2, severe hypotension or bradycardia, presence of atrioventricular block, cerebrovascular disease or hepatic dysfunction
Key Trial Info
Start Date :
January 5 2018
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
November 20 2019
Estimated Enrollment :
80 Patients enrolled
Trial Details
Trial ID
NCT03362021
Start Date
January 5 2018
End Date
November 20 2019
Last Update
September 22 2020
Active Locations (1)
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1
Attikon University Hospital
Athens, Attica, Greece, 12462