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Changes in Vaginal, Cervical and Uterine Microflora With Levonorgestrel Intrauterine Device Placement

This study has been completed.
Sponsor:
Collaborator:
Bayer
Information provided by (Responsible Party):
University of Utah
ClinicalTrials.gov Identifier:
NCT01496898
First received: August 21, 2011
Last updated: January 11, 2016
Last verified: January 2016
No Study Results Posted on ClinicalTrials.gov for this Study
  Study Status: This study has been completed.
  Study Completion Date: July 2013
  Primary Completion Date: December 2011 (Final data collection date for primary outcome measure)
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):