Phase
Condition
Contraception
Treatment
N/AClinical Study ID
Female Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Any subject receiving a Mirena® (levonorgestrel intrauterine device) for standardindications.
Subjects who received nonsteroidal anti-inflammatory drugs (NSAIDS) will not beexcluded.
Exclusion
Exclusion Criteria:
Subjects do not desire to be involved in the study
Subjects who have taken narcotics.
If the Mirena® (levonorgestrel intrauterine device) is not able to be successfullyplaced.
If cervical dilation is required, these subjects will be placed in a separate subsetand will be reported on separately.
Subject has allergy to lidocaine.
Study Design
Study Description
Connect with a study center
University of Tennessee Chattanooga Department of Obstetrics and Gynecology
Chattanooga, Tennessee 37403
United StatesActive - Recruiting
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