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Completed

NCT Number: NCT02070692

Tamoxifen for the Treatment of Unfavorable Bleeding in Contraceptive Implant Users

The purpose of this study is to study whether a drug called tamoxifen can reduce vaginal bleeding in women who are using the Etonogestrel contraceptive implant.

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Key information

Age range

15 year–45 year

Sex eligibility

Female

Study type

Interventional

Phase

Phase 4

Primary location

Oregon Health & Science University (OHSU)

Portland, Oregon, 97239, United States

About this study

Nearly all of the 3 million unintended pregnancies in the United States each year result from inconsistent or non-use of contraception. Increasing use of the most effective methods of contraception will reduce unintended pregnancies and their social, medical and economic consequences. The contraceptive etonogestrel implant (ENG implant) is 20 times more effective at pregnancy prevention than oral contraceptive pills, but it has bleeding side effects that make it unappealing for many women. Tamoxifen, a selective estrogen receptor modulator (SERM) used most commonly for adjuvant treatment of breast cancer, has previously been shown to dramatically reduce bleeding in users of an older levonorgestrel-based contraceptive implant (Norplant tm). It has not been studied in newer progestin-based methods such as the ENG implant. If tamoxifen could stop bleeding in users of the ENG implant, it would give patients and physicians a valuable option for management of progestin-induced irregular bleeding. This research project will test the effectiveness of tamoxifen taken on an as-needed basis to treat abnormal bleeding in ENG implant users. If tamoxifen can be established as an effective treatment for frequent or prolonged bleeding, it will increase the acceptability of the ENG implant, increase its use and reduce unintended pregnancies. This is the first project to evaluate tamoxifen for treatment of unfavorable bleeding in users of the ENG contraceptive implant.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Current user of the etonogestrel implant (Nexplanon, Implanon) for at least one month
  • Experiencing bleeding episodes more frequently than every 24 days, or a single episode of bleeding lasting longer than 14 days
  • English or Spanish speaking
  • Planning to continue implant use for six months
  • Access to a cell phone that can accept and send text messages

Exclusion criteria

  • Postpartum within six months
  • Post-abortion within six weeks
  • Pregnant
  • Breast-feeding
  • Undiagnosed abnormal uterine bleeding pre-dating placement of contraceptive implant
  • Bleeding dyscrasia
  • Anticoagulation use
  • Active cervicitis
  • Allergy to tamoxifen
  • History of venous thromboembolism
  • Current or past breast or uterine malignancy
  • Use of medication contraindicated with tamoxifen (coumadin, letrozole, bromocriptine, rifampicin, aminoglutethimide, phenobarbital)

Treatment and study plan

Tamoxifen

Drug

7 day course of tamoxifen during an episode of irregular vaginal bleeding

Other names: Nolvadex

Placebo

Drug

7 day course of placebo during an episode of irregular vaginal bleeding

Primary outcomes

  1. Bleeding Days

    Time frame: 180 days

    The primary objective of this study is to determine whether tamoxifen taken by users of the ENG implant on an as-needed basis for frequent or prolonged bleeding can reduce the number of bleeding days by at least 40% over 180 days, when compared to placebo.

  2. Bleeding/Spotting Days

    Time frame: 30 days

    Bleeding/spotting days

  3. Consecutive Bleeding-free Days After Study Drug

    Time frame: up to 180 days

    Consecutive bleeding-free days after study drug

Secondary outcomes

  1. Satisfaction (as Recorded on a 100mm Visual Analog Scale Where 0 is Not at All Satisfied and 100mm is Completely Satisfied)

    Time frame: 180 days

    Secondary objective is to determine whether tamoxifen can improve satisfaction with the implant and with bleeding patterns.

  2. Number of Participants Experiencing Ovulation After First Use of Study Drug

    Time frame: 30 days

    A third secondary objective is to determine whether taking tamoxifen at this dose compromises ovulation suppression in ENG users. Tamoxifen is known to transiently raise serum estradiol levels, but does not affect gonadotropin release in premenopausal women. Therefore, it is unlikely to interact with the ovulation suppression provided by the implant. However, to further investigate any theoretical interaction between tamoxifen and etonogestrel, urine markers of ovulation will be collected to document ongoing ovulation suppression with intermittent tamoxifen use.

Sponsors and collaborators

Lead sponsor

Oregon Health and Science University

Other

Collaborators

  • Society of Family Planning

Registry information

Official study title

Tamoxifen for the Treatment of Unfavorable Bleeding Patterns in Etonogestrel Contraceptive Implant Users

Important dates

Study start
2014
Primary completion
2015
Study completion
2015
First posted
Feb 25, 2014
Registry last updated
Jul 2, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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