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Terminated Phase 3 Interventional Results available

Minimize Menorrhagia in Women With Von Willebrand Disease

ClinicalTrials.gov ID: NCT02606045

Public ClinicalTrials.gov record NCT02606045. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 21, 2026, 4:51 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Prospective, Randomized, Crossover Trial Comparing Recombinant Von Willebrand Factor (rVWF) vs. Tranexamic Acid (TA) to Minimize Menorrhagia in Women With Von Willebrand Disease: The VWD Minimize Study

Study identification

NCT ID
NCT02606045
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Margaret Ragni
Other
Enrollment
39 participants

Conditions and interventions

Interventions

  • recombinant von Willebrand factor Drug
  • tranexamic acid Drug

Drug

Eligibility (public fields only)

Age range
13 Years to 45 Years
Sex
Female
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Feb 6, 2019
Primary completion
Apr 29, 2022
Completion
Aug 29, 2022
Last update posted
Jun 30, 2024

2019 – 2022

United States locations

U.S. sites
19
U.S. states
16
U.S. cities
19
Facility City State ZIP Site status
Banner MD Anderson Cancer Center Gilbert Arizona 85234
Center for Inherited Blood Disorders (CIBD) Orange California 92868
University of California San Francisco San Francisco California 94117
Emory University Afflac Blood Disorders Center Atlanta Georgia 30322
Henry Ford Hospital Medical Center Detroit Michigan 48202
Michigan State University East Lansing Michigan 48824
Mayo Clinic Rochester Minnesota 55902
Washington University St. Louis St Louis Missouri 63110
Cure4thekids Foundation Las Vegas Nevada 89135
Rutgers Robert Wood Johnson Medical School New Brunswick New Jersey 08901
State University of New York Upstate Medical Center Syracuse New York 13210
Cleveland Clinic Foundation Cleveland Ohio 44195
Ohio State University Wexner Medical Center Columbus Ohio 43210
Oregon Health and Science University Portland Oregon 97239
University of Pittsburgh and Hemophilia Center Western PA Pittsburgh Pennsylvania 15213
Vanderbilty University Nashville Tennessee 37322
University of Utah Salt Lake City Utah 84132
Bloodworks Northwest Seattle Washington 98104
Versiti Blood Center of Wisconsin Milwaukee Wisconsin 53226

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02606045, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jun 30, 2024 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02606045 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →