RAMBLE - Rivaroxaban vs. Apixaban for Heavy Menstrual Bleeding

Last updated: October 23, 2023
Sponsor: Indiana University
Overall Status: Completed

Phase

2/3

Condition

Thromboembolism

Venous Thromboembolism

Venous Thrombosis

Treatment

Rivaroxaban

Apixaban

Clinical Study ID

NCT02829957
RAMBLE
  • Ages 18-50
  • Female

Study Summary

A large proportion of women with menstruating potential with newly diagnosed VTE or atrial fibrillation, treated with apixaban will have less menstrual blood loss than patients randomized to rivaroxaban.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Non-pregnant women, age 18-50
  • For study purposes, evidence of negative pregnancy is accounted for by thetreating physician's initiation of treatment with oral anticoagulants
  • Objectively diagnosed VTE or atrial fibrillation/flutter
  • Patient reported active menstruation - does not apply to women who were recentlypregnant
  • Clinical plan and patient agreement to treat with oral anticoagulation for 3 months orlonger
  • Patients must have a working telephone

Exclusion

Exclusion Criteria:

  • Package insert exclusions for Eliquis (Apixban) or Xarelto (Rivaroxaban): [activepathological bleeding or severe hypersensitivity reaction to XARELTO or ELIQUIS (e.g.,anaphylactic reactions)]
  • Plan to become pregnant in the next three months.
  • Concomitant prescribed use of aspirin or thienopyridenes or other platelet inhibitingdrugs
  • Plan for surgical hysterectomy or endometrial ablation
  • Known uterine cancer
  • Von Willebrand's disease, or hemophilia
  • Known coagulopathy from liver disease
  • Conditions likely to preclude adherence to study procedures: Active intravenous druguse, known alcoholism, homelessness, or uncontrolled psychiatric illness.

Study Design

Total Participants: 19
Treatment Group(s): 2
Primary Treatment: Rivaroxaban
Phase: 2/3
Study Start date:
September 01, 2016
Estimated Completion Date:
February 13, 2020

Study Description

Heavy menstrual bleeding (HMB) complicates the treatment of approximately 9-25% of patients treated with orally administered anti-Xa anticoagulants for venous thromboembolism (VTE, including either pulmonary embolism or deep vein thrombosis). In particular, recent evidence has suggested an increase in length and severity of menstrual bleeding for women treated with rivaroxaban, and this effect may be less severe apixaban treatment.(1;2) Increase in uterine bleeding with rivaroxaban has necessitated hysterectomy in rare cases.(3) Other complications of HMB include reduced drug adherence, decreased perception of wellness (quality of life) and anemia.(4;5) The anti-Xa agents may increase HMB more than vitamin K antagonists.(1) However, in the principal investigators' experience treating over 100 women of menstruating age with rivaroxaban for VTE with varying degree of HMB, no woman has expressed desire to switch to a VKA even when offered this option (unpublished data). We have successfully reduced perception of HMB by switching from rivaroxaban to apixaban in six patients. Comparison of published and supplemental data from AMPLIFY and AMPLIFY Extend to EINSTEIN and EINSTEIN extend trials also support a lower rate of uterine bleeding with apixaban compared with rivaroxaban, although exact comparisons are difficult to make.(6;9) Myers et al recently reported a 9.4% rate of HMB with apixaban, compared with a 25% rate of HMB with rivaroxaban.(2) Accordingly, we hypothesize that women with menstruating potential with newly diagnosed VTE or atrial fibrillation/flutter, treated with apixaban will have less menstrual blood loss than patients randomized to rivaroxaban.

Connect with a study center

  • Eskenazi Health System

    Indiananapolis, Indiana 46202
    United States

    Site Not Available

  • Eskenazi Health System

    Indianapolis, Indiana 46202
    United States

    Site Not Available

  • Indiana University Health Methodist Hospital

    Indianapolis, Indiana 46202
    United States

    Site Not Available

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