Hemophilia pain mystery: new study aims to uncover hidden suffering
NCT ID NCT05202951
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study surveys 350 adults with hemophilia to better understand chronic pain—its type, location, and impact on daily life. Participants fill out questionnaires about their pain history, medication use, and emotional well-being. The goal is to help doctors recognize and treat pain more effectively in this population.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could lead to better pain management strategies for people with hemophilia by identifying pain patterns and raising awareness among doctors.
- What could go wrong
- This is an observational survey, not a treatment trial. It will not directly improve pain, and results may not apply to all patients due to language or internet access limits.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 350 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Feb 2022
- Expected to finish
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Sep 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Patients with hemophilia
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Patient with haemophilia of any severity, * Carrier female with low levels haemophilia (\< 40%), * ≥ 18 years of age and capable of giving informed consent to participate in research. Exclusion Criteria: * Patient's refusal to participate in the survey, * Patient does not understand enough French (written and spoken) to complete the survey, * Patient unable to complete the survey for logistical reasons (lack of internet access), * Patient under protective measures (guardianship), * Patients with known addictive comorbidities and/or cognitive disorders.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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CH Métropole Savoie
Chambéry, France
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CHU de Bordeaux
Bordeaux, France
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CHU de Clermont-Ferrand
Clermont-Ferrand, 63000, France
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CHU de Grenoble
Grenoble, France
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CHU de LILLE
Lille, France
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CHU de Saint-Etienne
Saint-Etienne, France
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CHU de TOULOUSE
Toulouse, France
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Centre Hospitalier Universitaire de Caen Normandie
Caen, France
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Centre Hospitalier Universitaire de Nantes
Nantes, France
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Hospices Civils de Lyon
Lyon, France
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