Copper IUD Treatment Observation Study

Completed · Phase 4 · Has a placebo group

Conditions studied: Menorrhagia

In brief

Studies indicate that bleeding irregularities and dysmenorrhea are common reasons for copper IUD method discontinuation. Some evidence suggests that non-steroidal anti-inflammatory medications (NSAIDs) can help improve bleeding during Cu-IUD use. However, these studies did not examine NSAID use with the TCu380A specifically, nor did they evaluate readily available NSAIDs such as over-the-counter naproxen. For this reason, the investigators propose a pilot trial in which new TCu380A users complaining of heavy or prolonged menstrual bleeding or spotting after 1 month of use are randomized to naproxen or placebo to be taken the first 7 days of menstruation for three consecutive cycles, and then observed for one cycle without treatment.

Key facts

Study ID

NCT02519231

Run by

University of Washington

People needed

34

Starts

2016-02-01

Expected to finish

2017-11-01

Last updated by the study team

2020-10-14

Who can join

Age: 18 and older, up to 49. Sex: female. Healthy volunteers: accepted.

You may qualify if…

• • Age ≥ 18 and < 49 years. We are including a wide range of ages because women of all ages request TCu380A. While we recognize that some women approaching menopause (median age = 51.4 years) may have changes in their baseline menstruation, we trust that clinicians enrolling the patients into the study will ensure that these women meet all inclusion (i.e., regular cycles) and exclusion criteria (i.e., do not have diagnosis of menorrhagia).
• Requesting to have TCu380A IUD inserted as contraceptive method.
• English-speaking.
• Regular menstrual cycles ranging 21-35 days apart.
• Generally healthy.
• Willing to attend a 4- to 6-week follow-up visit and complete surveys.

You may not qualify if…

• Known or suspected pregnancy.
• Contraindications to NSAID use. This includes underlying heart failure, chronic renal disease, chronic liver disease, peptic ulcer disease, or history of upper gastrointestinal bleed, and allergy to NSAIDs.
• Current regular use of a NSAID.
• Unwilling to avoid use of NSAIDs (except for study medication) for the duration of the study.
• Current diagnosis of menorrhagia, metrorrhagia, symptomatic uterine fibroids, or endometrial polyps.
• Use of depot medroxyprogesterone acetate (DMPA) or levonorgestrel-releasing intrauterine device (LNG IUD) within the previous 3 months.
• Postpartum in the past 4 weeks. The average day in which non-breastfeeding postpartum women ovulate is 25 days after birth, indicating that menstrual cycles can resume after the 4th postpartum week.
• Existing medical condition for which placement of TCu380A IUD is a contraindication according to the Centers for Disease Control and Prevention Medical Eligibility Criteria (MEC 4 medical conditions; see Appendix A).
• Currently breastfeeding.
• Previous use of the TCu380A.

Where it is running

• John H Stroger Jr Hospital of Cook County — Chicago, Illinois, United States
• Harborview Medical Center — Seattle, Washington, United States
• UW Neighborhood Clinic Northgate — Seattle, Washington, United States
• Hall Health Center — Seattle, Washington, United States
• University of Washington Medical Centers — Seattle, Washington, United States

Full record on ClinicalTrials.gov

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