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NCT07719647Not yet recruiting

Ultrasound Assessment of Joint Health in Patients With Mild Hemophilia (Factor Levels 5-40%)

Source: ClinicalTrials.gov · Last updated 17 Aug 2026

Brief summary (registry, in English)

Currently, few recommendations exist for patients with mild hemophilia, who represent approximately 60% of the hemophilia population. This study aims to provide objective data on joint health in these patients, which are currently limited compared to those with moderate or severe hemophilia. The use of joint ultrasound in mild hemophilia could allow early, asymptomatic detection of joint damage, support tailored management including patient education, and ultimately improve quality of life. The study will also explore the correlation between coagulation factor levels (FVIII or FIX) and other indicators of joint health in France.

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
150 (estimated)
First submitted
17 Jul 2026
Start date
Feb 2027
Primary completion date
Feb 2028
Lead sponsor
Assistance Publique - Hôpitaux de Paris
Diseases
Haemophilia
NCT number
NCT07719647

What you commit to

  • Study type: Interventional
  • Planned participants: 150
  • From Feb 2027 to the primary completion date, Feb 2028
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Patient on prophylactic treatment, defined as at least one of the following:
    • ≥5 factor concentrate injections per month for a period of more than 6 months o. Treatment with emicizumab o. Last factor concentrate injection within the past 28 days

Other illness

  • Patient with uncontrolled chronic rheumatologic disease, such as rheumatoid arthritis, inflammatory spondyloarthropathies, or microcrystalline arthritis.

Other

  • Patient with acquired hemophilia.
  • Known pregnancy or breastfeeding.
  • Patient deprived of liberty or under legal guardianship or conservatorship.

Who the study is looking for

  • Adult (≥18 years old) with congenital mild hemophilia, defined as historical coagulation factor level \>5% and \<40% (FVIII or FIX).
  • Affiliated with a social security system.
  • Provided written informed consent to participate in the study.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Hopital Necker Enfants Malades
Coordinator of this site? Confirm its status
ParisFranceUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.