Status:
TERMINATED
Intravenous Sedation Versus General Anesthesia in Patients Undergoing Minor Gynecologic Surgery
Lead Sponsor:
Northwestern University
Conditions:
Surgery
Anesthesia
Eligibility:
FEMALE
18+ years
Phase:
NA
Brief Summary
The use of deep sedation may improve the quality of recovery of patients undergoing minor gynecologic procedures. These patients may also have shorter hospital stays and potentially lower healthcare c...
Detailed Description
Once consent for the study has been obtained subjects will be randomly allocated into 2 groups, using a computer generated table of random numbers. Anesthetic management will be standardized (Appendix...
Eligibility Criteria
Inclusion
- Female patients undergoing second trimester abortions:
- Pregnancy: 12-24 weeks gestational size
- ASA PS I and II
- No history of diabetes mellitus, GERD or sleep apnea
- Age: \> 18 years of age
- Fluent in English
Exclusion
- ASA PSIII, Emergency surgery
- Pregnancy: \> 24 weeks gestational size
- Age: \< 18 years of age
- Diabetes mellitus
- Gastroesophageal reflux disease
- Hiatal hernia
- Obstructive sleep apnea
- Coagulopathy
- Chronic pain syndromes
- Chronic opioid dependency
- Alcohol or illicit drug abuse
- BMI: \> 35Kg/m2
- Allergy to study protocol drugs
- Drop out criteria:
- Subjects withdrawal of consent.
- Subjects who experience massive bleeding intraoperatively, will be excluded from the final data analysis
Key Trial Info
Start Date :
October 19 2012
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
April 17 2014
Estimated Enrollment :
19 Patients enrolled
Trial Details
Trial ID
NCT01890707
Start Date
October 19 2012
End Date
April 17 2014
Last Update
January 2 2020
Active Locations (1)
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1
Prentice Womens' Hospital
Chicago, Illinois, United States, 60611