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Sponsored by: |
Oregon Health and Science University |
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Information provided by: | Oregon Health and Science University |
ClinicalTrials.gov Identifier: | NCT00562276 |
The purpose of this multi-center clinical trial is to evaluate the safety and effectiveness of inserting an intrauterine device (IUD) immediately after a suction aspiration procedure compared to inserting the IUD 2-6 weeks after the procedure. This study will also evaluate how satisfied women are with the timing of their IUD placement. Subjects will be able to choose between the Paraguard IUD or the Mirena IUD.
The researchers hypothesize that:
Condition | Intervention | Phase |
---|---|---|
Contraception |
Procedure: Immediate IUD insertion |
Phase IV |
Study Type: | Interventional |
Study Design: | Prevention, Randomized, Double Blind (Subject, Caregiver, Investigator), Parallel Assignment, Safety/Efficacy Study |
Official Title: | Immediate Versus Delayed IUD Insertion Following Suction Aspiration Between 5 and 12 Weeks Gestation: a Randomized Trial |
Estimated Enrollment: | 578 |
Study Start Date: | May 2007 |
Estimated Study Completion Date: | July 2009 |
Estimated Primary Completion Date: | July 2009 (Final data collection date for primary outcome measure) |
Arms | Assigned Interventions |
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1: Experimental
Immediate IUD insertion following suction aspiration between 5 and 12 weeks gestation
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Procedure: Immediate IUD insertion
Insertion of either Paraguard or Mirena IUD within minutes of completing suction aspiration procedure between 5 and 12 weeks gestation
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2: No Intervention
Delayed IUD insertion 2-6 weeks following suction aspiration between 5 and 12 weeks gestation
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Ages Eligible for Study: | 18 Years and older |
Genders Eligible for Study: | Female |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Intrauterine pregnancy documented with ultrasound. For women with a gestational sac, the gestational age (EGA) must be ≥ 5 weeks 0 days but ≤ 12 weeks 0 days based on the following criteria:
Exclusion Criteria:
Contact: Women's Health Research Unit Confidential Recruitment Line | (503) 494-3666 | whru@ohsu.edu |
United States, Georgia | |
Emory University | Recruiting |
Atlanta, Georgia, United States | |
Contact: Carrie Cwiak, MD, MPH ccwiak@emory.edu | |
Principal Investigator: Carrie Cwiak, MD, MPH | |
United States, New Mexico | |
University of New Mexico | Recruiting |
Albuquerque, New Mexico, United States | |
Contact: Eve Espey, MD, MPH eespey@salud.unm.edu | |
Principal Investigator: Eve Espey, MD, MPH | |
United States, New York | |
Jacobi Medical Center | Active, not recruiting |
Bronx, New York, United States | |
United States, Pennsylvania | |
University of Pittsburgh School of Medicine | Recruiting |
Pittsburgh, Pennsylvania, United States | |
Contact: Matthew Reeves, MD, MPH mreeves@mail.magee.edu | |
Principal Investigator: Matthew Reeves, MD, MPH |
Principal Investigator: | Paula H Bednarek, MD | Oregon Health and Science University |
Responsible Party: | OHSU ( Paula Bednarek, MD, MPH ) |
Study ID Numbers: | OHSU FAMPLAN 2535 |
Study First Received: | November 21, 2007 |
Last Updated: | February 4, 2009 |
ClinicalTrials.gov Identifier: | NCT00562276 History of Changes |
Health Authority: | United States: Institutional Review Board |
IUD insertion timing |
Levonorgestrel |