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RAMBLE - Rivaroxaban vs. Apixaban for Heavy Menstrual Bleeding (RAMBLE)

Primary Purpose

Venous Thromboembolism, Menstruation

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Apixaban
Rivaroxaban
Sponsored by
Indiana University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Venous Thromboembolism

Eligibility Criteria

18 Years - 50 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Non-pregnant women, age 18-50

    • For study purposes, evidence of negative pregnancy is accounted for by the treating 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 recently pregnant
  • Clinical plan and patient agreement to treat with oral anticoagulation for 3 months or longer
  • Patients must have a working telephone

Exclusion Criteria:

  • Package insert exclusions for Eliquis (Apixban) or Xarelto (Rivaroxaban): [active pathological 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 inhibiting drugs
  • 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 drug use, known alcoholism, homelessness, or uncontrolled psychiatric illness.

Sites / Locations

  • Eskenazi Health System
  • Indiana University Health Methodist Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Rivaroxaban

Apixaban

Arm Description

Outcomes

Primary Outcome Measures

PBAC Scores
Measure Description: A PBAC Score of < 100 indicates a normal menstrual cycle. The lowest possible score would be zero. Higher values indicate worse outcomes. The higher theoretical range value cannot be calculated. The scoring mechanism is as follows; Towels 1 point for each lightly stained towel 5 points or each moderately soiled towel 20 points if the towel is completely saturated with blood Tampons 1 point for each lightly stained tampon 5 points for each moderately soiled tampon 10 points if the tampon is completely saturated with blood Clots 1 point for small clots 5 points for large clots

Secondary Outcome Measures

Number of Participants Who Discontinued Planned Drug Administration
Number of Patients That Held Drug for Menorrhagia
Number of Participants With Major Hemorrhage
Number of Participants With Venous Thromboembolism (VTE)
Number of Participants Who Crossed Over to Another Anticoagulant
Number of Participants With Clinically Relevant Non-major Bleeding
Hemoglobin Concentration
Measure Description: Normal hemoglobin range for adult women - 12 - 16 g/dL. Lower levels indicate worse outcomes.
Physical Component Summary of Standard From 36
The RAND 36-Item Health Survey (Version 1.0) taps eight health concepts: physical functioning, bodily pain, role limitations due to physical health problems, role limitations due to personal or emotional problems, emotional well-being, social functioning, energy/fatigue, and general health perceptions. All items are scored so that a high score defines a more favorable health state. In addition, each item is scored on a 0 to 100 range so that the lowest and highest possible scores are 0 and 100, respectively.

Full Information

First Posted
July 6, 2016
Last Updated
April 18, 2023
Sponsor
Indiana University
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1. Study Identification

Unique Protocol Identification Number
NCT02829957
Brief Title
RAMBLE - Rivaroxaban vs. Apixaban for Heavy Menstrual Bleeding
Acronym
RAMBLE
Official Title
Randomized Trial to Test the Effect of Rivaroxaban or Apixaban on Menstrual Blood Loss in Women
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Completed
Study Start Date
September 2016 (undefined)
Primary Completion Date
February 13, 2020 (Actual)
Study Completion Date
February 13, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Indiana University

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief 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.
Detailed 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Venous Thromboembolism, Menstruation

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
19 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Rivaroxaban
Arm Type
Active Comparator
Arm Title
Apixaban
Arm Type
Active Comparator
Intervention Type
Drug
Intervention Name(s)
Apixaban
Other Intervention Name(s)
Eliquis
Intervention Description
10mg BID for 7 days, then 5mg BID for three months
Intervention Type
Drug
Intervention Name(s)
Rivaroxaban
Other Intervention Name(s)
Xarelto
Intervention Description
15mg BID for 7 days, then 20mg daily for three months
Primary Outcome Measure Information:
Title
PBAC Scores
Description
Measure Description: A PBAC Score of < 100 indicates a normal menstrual cycle. The lowest possible score would be zero. Higher values indicate worse outcomes. The higher theoretical range value cannot be calculated. The scoring mechanism is as follows; Towels 1 point for each lightly stained towel 5 points or each moderately soiled towel 20 points if the towel is completely saturated with blood Tampons 1 point for each lightly stained tampon 5 points for each moderately soiled tampon 10 points if the tampon is completely saturated with blood Clots 1 point for small clots 5 points for large clots
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Number of Participants Who Discontinued Planned Drug Administration
Time Frame
3 months
Title
Number of Patients That Held Drug for Menorrhagia
Time Frame
1, 2, and 3 months
Title
Number of Participants With Major Hemorrhage
Time Frame
3 months
Title
Number of Participants With Venous Thromboembolism (VTE)
Time Frame
3 months
Title
Number of Participants Who Crossed Over to Another Anticoagulant
Time Frame
3 months
Title
Number of Participants With Clinically Relevant Non-major Bleeding
Time Frame
3 months
Title
Hemoglobin Concentration
Description
Measure Description: Normal hemoglobin range for adult women - 12 - 16 g/dL. Lower levels indicate worse outcomes.
Time Frame
3 months
Title
Physical Component Summary of Standard From 36
Description
The RAND 36-Item Health Survey (Version 1.0) taps eight health concepts: physical functioning, bodily pain, role limitations due to physical health problems, role limitations due to personal or emotional problems, emotional well-being, social functioning, energy/fatigue, and general health perceptions. All items are scored so that a high score defines a more favorable health state. In addition, each item is scored on a 0 to 100 range so that the lowest and highest possible scores are 0 and 100, respectively.
Time Frame
3 months

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Non-pregnant women, age 18-50 For study purposes, evidence of negative pregnancy is accounted for by the treating 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 recently pregnant Clinical plan and patient agreement to treat with oral anticoagulation for 3 months or longer Patients must have a working telephone Exclusion Criteria: Package insert exclusions for Eliquis (Apixban) or Xarelto (Rivaroxaban): [active pathological 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 inhibiting drugs 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 drug use, known alcoholism, homelessness, or uncontrolled psychiatric illness.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jeffrey A Kline, MD
Organizational Affiliation
Indiana University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Eskenazi Health System
City
Indianapolis
State/Province
Indiana
ZIP/Postal Code
46202
Country
United States
Facility Name
Indiana University Health Methodist Hospital
City
Indianapolis
State/Province
Indiana
ZIP/Postal Code
46202
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
26272306
Citation
De Crem N, Peerlinck K, Vanassche T, Vanheule K, Debaveye B, Middeldorp S, Verhamme P, Peetermans M. Abnormal uterine bleeding in VTE patients treated with rivaroxaban compared to vitamin K antagonists. Thromb Res. 2015 Oct;136(4):749-53. doi: 10.1016/j.thromres.2015.07.030. Epub 2015 Aug 4.
Results Reference
background
PubMed Identifier
26970315
Citation
Myers B, Webster A. Heavy menstrual bleeding on Rivaroxaban - Comparison with Apixaban. Br J Haematol. 2017 Mar;176(5):833-835. doi: 10.1111/bjh.14003. Epub 2016 Mar 11. No abstract available.
Results Reference
background
PubMed Identifier
26113241
Citation
Beam DM, Kahler ZP, Kline JA. Immediate Discharge and Home Treatment With Rivaroxaban of Low-risk Venous Thromboembolism Diagnosed in Two U.S. Emergency Departments: A One-year Preplanned Analysis. Acad Emerg Med. 2015 Jul;22(7):788-95. doi: 10.1111/acem.12711. Epub 2015 Jun 25.
Results Reference
background
PubMed Identifier
27143861
Citation
Kline JA, Kahler ZP, Beam DM. Outpatient treatment of low-risk venous thromboembolism with monotherapy oral anticoagulation: patient quality of life outcomes and clinician acceptance. Patient Prefer Adherence. 2016 Apr 15;10:561-9. doi: 10.2147/PPA.S104446. eCollection 2016.
Results Reference
background
PubMed Identifier
17532811
Citation
Liu Z, Doan QV, Blumenthal P, Dubois RW. A systematic review evaluating health-related quality of life, work impairment, and health-care costs and utilization in abnormal uterine bleeding. Value Health. 2007 May-Jun;10(3):183-94. doi: 10.1111/j.1524-4733.2007.00168.x.
Results Reference
background
PubMed Identifier
23808982
Citation
Agnelli G, Buller HR, Cohen A, Curto M, Gallus AS, Johnson M, Masiukiewicz U, Pak R, Thompson J, Raskob GE, Weitz JI; AMPLIFY Investigators. Oral apixaban for the treatment of acute venous thromboembolism. N Engl J Med. 2013 Aug 29;369(9):799-808. doi: 10.1056/NEJMoa1302507. Epub 2013 Jul 1.
Results Reference
background
PubMed Identifier
21128814
Citation
EINSTEIN Investigators; Bauersachs R, Berkowitz SD, Brenner B, Buller HR, Decousus H, Gallus AS, Lensing AW, Misselwitz F, Prins MH, Raskob GE, Segers A, Verhamme P, Wells P, Agnelli G, Bounameaux H, Cohen A, Davidson BL, Piovella F, Schellong S. Oral rivaroxaban for symptomatic venous thromboembolism. N Engl J Med. 2010 Dec 23;363(26):2499-510. doi: 10.1056/NEJMoa1007903. Epub 2010 Dec 3.
Results Reference
background
PubMed Identifier
22449293
Citation
EINSTEIN-PE Investigators; Buller HR, Prins MH, Lensin AW, Decousus H, Jacobson BF, Minar E, Chlumsky J, Verhamme P, Wells P, Agnelli G, Cohen A, Berkowitz SD, Bounameaux H, Davidson BL, Misselwitz F, Gallus AS, Raskob GE, Schellong S, Segers A. Oral rivaroxaban for the treatment of symptomatic pulmonary embolism. N Engl J Med. 2012 Apr 5;366(14):1287-97. doi: 10.1056/NEJMoa1113572. Epub 2012 Mar 26.
Results Reference
background
PubMed Identifier
23216615
Citation
Agnelli G, Buller HR, Cohen A, Curto M, Gallus AS, Johnson M, Porcari A, Raskob GE, Weitz JI; AMPLIFY-EXT Investigators. Apixaban for extended treatment of venous thromboembolism. N Engl J Med. 2013 Feb 21;368(8):699-708. doi: 10.1056/NEJMoa1207541. Epub 2012 Dec 8.
Results Reference
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RAMBLE - Rivaroxaban vs. Apixaban for Heavy Menstrual Bleeding

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