Status:
TERMINATED
Comparing the Effectiveness of Oral Versus Intravenous Pain Medicine for Suction Curettage (D&C)
Lead Sponsor:
Planned Parenthood League of Massachusetts
Conditions:
Undesired Pregnancy
Eligibility:
FEMALE
18+ years
Phase:
NA
Brief Summary
The main objective of this study is to determine the equivalency of oral conscious sedation and intravenous conscious sedation for first trimester surgical abortion. We hypothesize that oral conscious...
Detailed Description
The main objective of this study is to determine the equivalency of oral conscious sedation (oxycodone 10mg PO plus lorazepam 1mg SL) and intravenous conscious sedation (fentanyl 100 µg plus midazolam...
Eligibility Criteria
Inclusion
- Age 18 or older.
- Undesired pregnancy between 6 0/7-12 6/7 weeks gestation.
- Has already signed consent for pregnancy termination.
- Eligible for IV sedation per clinic protocol.
Exclusion
- Under 120 lbs.
- Allergies to any of the drugs being studied.
- Chronic narcotics, barbiturates or benzodiazepine use within the past year.
- History of IV drug use within the last year.
- Inability to give informed consent.
- Does not speak English or Spanish and does not have translator for all study procedures
- Previously participated in study
Key Trial Info
Start Date :
June 1 2006
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
July 1 2007
Estimated Enrollment :
132 Patients enrolled
Trial Details
Trial ID
NCT00337792
Start Date
June 1 2006
End Date
July 1 2007
Last Update
March 18 2016
Active Locations (1)
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1
Planned Parenthood League of Massachusetts
Boston, Massachusetts, United States, 02215