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Trial record 50 of 416 for:    LEVONORGESTREL

Mirena Intrauterine System Timing of Insertion: A Randomized Controlled Trial (MISTIC)

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. Identifier: NCT01272960
Recruitment Status : Completed
First Posted : January 10, 2011
Results First Posted : December 2, 2017
Last Update Posted : December 2, 2017
Society of Family Planning
Information provided by (Responsible Party):
Washington University School of Medicine

Brief Summary:

In order to determine the timing of LNG-IUS insertion that results in a greater proportion of women using the LNG-IUS at 6-months post-partum, we will perform a randomized control trial of interval versus immediate post-placenta insertion. Women will be enrolled at 36-weeks gestation and greater. At the time of vaginal delivery, women will be randomized to receive either immediate post-placenta insertion of the LNG-IUS or routine insertion at 4-8 weeks post-partum. All patients will return at 4-6 weeks post-insertion and 6 months post-partum to confirm correct position of the LNG-IUS. The primary outcome of this sub-study is the number of LNG-IUS in the correct position at 6-months. Secondary outcomes include assessing the safety of post-placental LNG-IUS insertion and difference in acceptability and symptoms experienced by participants. This is a sub-study of the Contraceptive Choice Project, a prospective cohort study that aims to improve the use of long-acting contraception by removing financial barriers which has already enrolled over 5,000 patients. Association of this study with CHOICE offers unique advantages including infrastructure to support subject recruitment, retention and completion of follow-up as well as covering the cost of LNG-IUS devices.

We hypothesize that, despite higher expulsion rates, women randomized to receive the LNG-IUS immediately after placenta delivery will have higher rates of LNG-IUS continuation due to poor rates of follow up in the interval insertion group. This is likely to be particularly noticeable in our patient population, which is largely uninsured with poor access to healthcare. Further, typical symptoms of LNG-IUS insertion include bleeding and cramping, which may be disguised by the post-partum period. Published reports of immediate post-placenta insertion focus on expulsion rates and do not report on symptoms and satisfaction rates.

Condition or disease Intervention/treatment Phase
Postpartum Period Device: Post-Placenta Mirena Insertion Device: Interval Insertion Not Applicable

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 53 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Prevention
Official Title: Randomized, Open-label, Controlled Trial of Immediate Postpartum Versus Interval Insertion of Mirena to Increase the Usage at 6 Months After Delivery
Study Start Date : October 2010
Actual Primary Completion Date : December 2012
Actual Study Completion Date : December 2012

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Postpartum Care

Arm Intervention/treatment
Active Comparator: Interval Insertion
Will receive Mirena at 4-8 weeks post-partum after vaginal delivery.
Device: Interval Insertion
Insertion of Mirena 4-8 weeks post partum after vaginal delivery

Experimental: Post-Placental Mirena Insertion
Will receive Mirena insertion within 10 minutes of delivery of placenta
Device: Post-Placenta Mirena Insertion
Mirena(R) intrauterine device will be inserted within 10 minutes of delivery of the placenta

Primary Outcome Measures :
  1. Mirena in Place [ Time Frame: 6 months ]
    Proportion of women in each arm with Mirena in place at 6 months

Secondary Outcome Measures :
  1. Mirena Expulsion [ Time Frame: 6 weeks ]
    The percentage of patients with post-placental placement of Mirena who experience an expulsion

  2. Uterine Perforation [ Time Frame: 6 months ]
    The proportion of patients in each arm who experience a uterine perforation

  3. Intrauterine Infection [ Time Frame: 6 months ]
    The proportion of patients in each arm who experience an intrauterine infection (endometritis, pelvic inflammatory disease)

Information from the National Library of Medicine

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Ages Eligible for Study:   14 Years to 45 Years   (Child, Adult)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   Yes

Inclusion Criteria:

  • 14-45 years
  • Vaginal Delivery at Barnes-Jewish Hospital
  • Sexually active with male partner
  • No tubal ligation/hysterectomy
  • Not currently using contraception
  • Desire reversible contraception
  • Reside in St. Louis City/County
  • Requests Mirena(R) intrauterine device for contraception

Exclusion Criteria:

  • Allergy to Mirena(R) system
  • Cesarean delivery
  • Cervical cancer, breast cancer
  • Active liver disease
  • Untreated cervicitis
  • Uterine anomaly/fibroids preventing Mirena(R) placement
  • Delivery <36 weeks
  • Chorioamnionitis
  • Prolonged rupture of membranes (>18 hours)

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT01272960

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United States, Missouri
Barnes Jewish Hospital
Saint Louis, Missouri, United States, 63110
Sponsors and Collaborators
Washington University School of Medicine
Society of Family Planning
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Principal Investigator: Lorie M Harper, MD Washington University School of Medicine

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Responsible Party: Washington University School of Medicine Identifier: NCT01272960    
Other Study ID Numbers: SFP4-13
First Posted: January 10, 2011    Key Record Dates
Results First Posted: December 2, 2017
Last Update Posted: December 2, 2017
Last Verified: October 2017
Keywords provided by Washington University School of Medicine:
Postnatal care
Additional relevant MeSH terms:
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Contraceptive Agents, Female
Contraceptive Agents
Reproductive Control Agents
Physiological Effects of Drugs
Contraceptives, Oral, Synthetic
Contraceptives, Oral