Status:
COMPLETED
Paracervical Versus Intracervical Lidocaine
Lead Sponsor:
University of California, San Diego
Conditions:
Abortion, Induced
Pain
Eligibility:
FEMALE
18+ years
Phase:
NA
Brief Summary
The aim of this study is to estimate the efficacy of intracervical versus paracervical block on pain experienced during first trimester suction curettage without the use of preoperative cervical ripen...
Eligibility Criteria
Inclusion
- Women presenting for elective first trimester abortion
Exclusion
- Gestation over 12 weeks by ultrasound
- Weight less than 98 pounds
- Known allergy to lidocaine
- Known nonviable pregnancy
Key Trial Info
Start Date :
December 1 2007
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
February 1 2008
Estimated Enrollment :
89 Patients enrolled
Trial Details
Trial ID
NCT00816751
Start Date
December 1 2007
End Date
February 1 2008
Last Update
August 13 2019
Active Locations (1)
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1
Planned Parenthood
San Diego, California, United States, 92101