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Immediate Post-placental Insertion of the Copper T 380A After Cesarean Delivery Versus 6 Week Post-cesarean Insertion

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01293760
First Posted: February 11, 2011
Last Update Posted: May 10, 2012
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Collaborators:
Mulago Hospital, Uganda
Brigham and Women's Hospital
Society of Family Planning
Information provided by (Responsible Party):
Planned Parenthood League of Massachusetts
No Study Results Posted on ClinicalTrials.gov for this Study
  Study Status: This study has been completed.
  Study Completion Date: November 2011
  Primary Completion Date: November 2011 (Final data collection date for primary outcome measure)
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):