Status:
COMPLETED
Tenaculum Pain Control Study
Lead Sponsor:
Oregon Health and Science University
Conditions:
Cervical Pain
Pelvic Pain
Eligibility:
FEMALE
18+ years
Phase:
PHASE4
Brief Summary
The purpose of this clinical trial is to evaluate the effect of an intracervical lidocaine injection versus topical lidocaine gel on the pain experienced by patients undergoing tenaculum application t...
Detailed Description
Subjects who have already scheduled an IUD insertion or endometrial biopsy will be asked to join this study assessing two pain control interventions at the time of tenaculum application to the cervix ...
Eligibility Criteria
Inclusion
- Generally healthy women
- Age 18 and over
- Indication for endometrial biopsy or IUD placement
Exclusion
- Allergy to lidocaine or other local anesthetic
- Pregnancy, known or suspected
- Patients who are premedicated with misoprostol
- Patients with a chronic pain condition for which the patient takes daily pain medication
Key Trial Info
Start Date :
September 1 2011
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
May 1 2012
Estimated Enrollment :
74 Patients enrolled
Trial Details
Trial ID
NCT01421641
Start Date
September 1 2011
End Date
May 1 2012
Last Update
April 21 2014
Active Locations (1)
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1
Oregon Health & Science University
Portland, Oregon, United States, 97239