NCT00476021View on ClinicalTrials.gov

Postplacental or Delayed Insertion of the Levonorgestrel-releasing Intrauterine Device (IUD) After Vaginal Delivery

NACompletedINTERVENTIONAL
Enrollment

168

Participants

Timeline

Start Date

May 31, 2007

Primary Completion Date

October 31, 2008

Study Completion Date

October 31, 2008

Conditions
Contraception
Interventions
DEVICE

Levonorgestrel-releasing IUD (Mirena)

levonorgestrel-releasing IUD containing 52 mg levonorgestrel, indicated for use for up to 5 years

Trial Locations (1)

15213

Magee-Womens Hospital, University of Pittsburgh, Pittsburgh

All Listed Sponsors
lead

University of Pittsburgh

OTHER

NCT00476021 - Postplacental or Delayed Insertion of the Levonorgestrel-releasing Intrauterine Device (IUD) After Vaginal Delivery | Biotech Hunter | Biotech Hunter