Actively Recruiting
Prevention of Bleeding in Patients With Moderate and Severe Hemophilia A Playing Sports: A Comparison Between Factor VIII and Emicizumab Prophylaxis
Led by Wayne State University · Updated on 2026-01-16
72
Participants Needed
9
Research Sites
289 weeks
Total Duration
On this page
Sponsors
W
Wayne State University
Lead Sponsor
G
Genentech, Inc.
Collaborating Sponsor
AI-Summary
What this Trial Is About
Hemophilia A (HA) is a genetic bleeding disorder resulting from a deficiency or absence of factor VIII (FVIII), which is necessary in the clotting process. This disorder occurs mostly in males and in severe cases causes frequent bleeding episodes in joints and muscles which can lead to progressive damage that affects mobility and quality of life. Prophylactic FVIII administered intravenously every other day has been the standard of care treatment for HA for the past few decades. Sports and physical activity are generally encouraged in patients with hemophilia on appropriate prophylactic treatment to increase strength, prevent or decrease obesity, accrue and maintain bone density and encourage normal socialization. To ensure safety with participation in sports in persons with hemophilia A (PWHA), timing of FVIII administration is often adjusted to maximize FVIII at the time of sports. The exact factor level that is needed to safely participate in sports and minimize bleeding risk is not yet known. Based on clinical practice, infusion of FVIII to near the lower limit of normal right before participation in sports generally works to prevent bleeding. The study is looking at how well the newly approved medication Emicizumab works compared to Factor VIII to prevent bleeding in patients with Hemophilia A who play sports. The study will enroll children and adolescents who are already on Emicizumab or Factor VIII who are currently playing sports.
CONDITIONS
Official Title
Prevention of Bleeding in Patients With Moderate and Severe Hemophilia A Playing Sports: A Comparison Between Factor VIII and Emicizumab Prophylaxis
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Participant or parent/legal representative able to provide informed consent; minor able to provide assent if applicable
- Males and females aged 6 to 19 years with moderate to severe Hemophilia A (factor VIII activity ≤ 5%) without inhibitors
- Currently on Emicizumab or standard Factor VIII prophylaxis as recommended by a hematologist
- Engaged in or registered for sports with moderate to high risk of bleeding per NHF Playing it Safe guidelines (rating ≥ 2)
- Willing to keep activity, bleed, and treatment logs throughout the study
You will not qualify if you...
- Participant or parent/legal representative unwilling to provide informed consent or assent
- Unwilling to record bleeding and treatment information as required by the study
- Have any other bleeding disorders besides Hemophilia A
- Are pregnant, planning pregnancy, or breastfeeding
- Currently using both Factor VIII replacement and Emicizumab concurrently for sports participation
AI-Screening
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Trial Site Locations
Total: 9 locations
1
Arkansas Children's Hospital
Little Rock, Arkansas, United States, 72202
Actively Recruiting
2
Stanford University
Palo Alto, California, United States, 94304
Actively Recruiting
3
Rady Children's Hospital
San Diego, California, United States, 92123
Actively Recruiting
4
Johns Hopkins All Children's Hospital
St. Petersburg, Florida, United States, 33701
Actively Recruiting
5
Indiana Hemophilia & Thrombosis Center
Indianapolis, Indiana, United States, 46260
Actively Recruiting
6
Boston Children's Hospital
Boston, Massachusetts, United States, 02215
Actively Recruiting
7
Children's Hospital of Michigan
Detroit, Michigan, United States, 48201
Actively Recruiting
8
Cincinnati Children's Hospital Medical Center
Cincinnati, Ohio, United States, 45229
Actively Recruiting
9
Oklahoma Center for Bleeding and Clotting Disorders
Oklahoma City, Oklahoma, United States, 73104
Actively Recruiting
Research Team
A
Amy Stolinski, MPH
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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