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NCT05202951Active, not recruiting

Chronic Pain and Hemophilia

Status of Chronic Pain in Patients With Hemophilia.

Source: ClinicalTrials.gov · Last updated 29 May 2026

Brief summary (registry, in English)

Hemophilia (A and B) are X-linked hereditary bleeding disorders whose severity depends on the level of coagulation factor (FVIII or FIX respectively). Bleeding is mainly from joints (hemarthrosis) and muscles (hematoma). Nowadays, treatment is based on preventive or curative intravenous infusion of coagulation factor concentrates. Despite these treatments, there is joint deterioration that can be responsible for hemophilic arthropathy and chronic pain. This pain may be related to excess nociception during acute bleeding, but it may also be neuropathic. There are only a few studies that have looked at pain in hemophilia, but it is accepted that the vast majority of patients (especially those with severe forms) suffer from chronic pain. Because patients have become accustomed to this pain and physicians are still not very aware of how to assess it, this pain is not treated effectively. In order to better manage pain in hemophilia, it is therefore necessary to characterize their pain and to know the nociceptive or neuropathic component. The aim of our study is therefore to study the prevalence, the nociceptive or neuropathic profile, the chronic aspect of pain and the main locations of pain in hemophilia. In addition to raising the awareness of physicians in the centers about pain management using specific questionnaires, this survey will help to better define chronic pain in hemophilia of all severities.

Status (registry)
Active, not recruiting
Study type
Observational
Enrollment
350 (estimated)
First submitted
10 Jan 2022
Start date
28 Feb 2022
Primary completion date
18 Dec 2025
Lead sponsor
University Hospital, Clermont-Ferrand
Diseases
Haemophilia
NCT number
NCT05202951

What you commit to

  • Study type: Observational
  • Planned participants: 350
  • From 28 Feb 2022 to the primary completion date, 18 Dec 2025
  • 10 sites 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.

Other illness

  • Patients with known addictive comorbidities and/or cognitive disorders.

Other

  • 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),

Who the study is looking for

  • 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.

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

Full criteria on ClinicalTrials.gov

Sites (10)

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

SiteCityCountrySite status
CHU de Bordeaux
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BordeauxFranceUnknown status
Centre Hospitalier Universitaire de Caen Normandie
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CaenFranceUnknown status
CH Métropole-Savoie
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ChambéryFranceUnknown status
CHU de Clermont-Ferrand
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Clermont-FerrandFranceUnknown status
CHU de Grenoble
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GrenobleFranceUnknown status
CHU de Lille
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LilleFranceUnknown status
Hospices Civils de Lyon
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LyonFranceUnknown status
Centre Hospitalier Universitaire de Nantes
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NantesFranceUnknown status
Chu de Saint Etienne
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Saint-EtienneFranceUnknown status
CHU de Toulouse
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ToulouseFranceUnknown status

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