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Study identifier: NCT05916469 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Heavy Menstrual Bleeding Progestin Treatment in Bleeding Disorders Study

Condition: Heavy Menstrual Bleeding · Bleeding Disorder · Von Willebrand Diseases  ·  Sponsor: Oregon Health and Science University

PhaseN/A
Planned participants300
Who can joinFemale, 10 Years to 24 Years
Healthy volunteersNo

About this study

The goal of this multicenter prospective observational study and registry of U.S. adolescents and young adults with heritable bleeding disorders is to determine the bleeding outcomes, satisfaction, hemostatic parameter changes, and patient reported quality of life after 6 months of use of either of two commonly used hormonal treatments for menstrual suppression - levonorgestrel intrauterine device (LNG-IUD) and norethindrone acetate (NETA). Under this application the study will compare the two treatments and compare outcomes after LNG-IUD treatment results to a control group without a bleeding disorder, with the goal of determining the benefits and expected outcomes of these treatment options for this population.

This description comes directly from the study's public registry record.

Talk to the study team

OHSU Women's Health Research Unit  ·  5034943666  ·  whru@ohsu.edu

Maureen Baldwin, MD MPH  ·  5034949762  ·  schaum@ohsu.edu

Always discuss trial participation with your own doctor first.

Locations (9)

StanfordPalo Alto, California, United StatesNot Yet Recruiting
Colorado Anschutz Medical CampusAurora, Colorado, United StatesNot Yet Recruiting
EmoryAtlanta, Georgia, United StatesNot Yet Recruiting
University of Michigan MedicineAnn Arbor, Michigan, United StatesNot Yet Recruiting
Children's MercyKansas City, Missouri, United StatesNot Yet Recruiting
Oregon Health & Science UniversityPortland, Oregon, United StatesRecruiting
Penn State HealthHershey, Pennsylvania, United StatesNot Yet Recruiting
University of WashingtonSeattle, Washington, United StatesNot Yet Recruiting
Seattle Children's HospitalSeattle, Washington, United StatesNot Yet Recruiting

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Source record: clinicaltrials.gov/study/NCT05916469