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Study identifier: NCT07096349 Synced from ClinicalTrials.gov · July 29, 2026
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Multidimensional Assessment of Chronic Pain in Severe Haemophilia A

Condition: Hemophilia A Without Inhibitor  ·  Sponsor: Investigación en Hemofilia y Fisioterapia

PhaseN/A
Planned participants109
Who can joinMale, 18 Years to no upper limit
Healthy volunteersNo

About this study

Introduction: Haemophilia is a congenital coagulopathy characterised by haemarthrosis, mainly in the knees, ankles and elbows. Prophylactic treatment is the most effective therapeutic option for preventing or minimising these bleeds. Bispecific monoclonal antibodies have been shown to be effective in reducing bleeding in patients with haemophilia. Objectives: To investigate the associations between chronic residual pain and pain catastrophising, perceived self-efficacy regarding the disease and treatment, and body image and perception of visible disability. Methods. Multicentre cross-sectional cohort studies. 109 patients with severe haemophilia A from different regions of Spain will be included in the study. The primary variable will be chronic residual pain and its functional interference (Brief Pain Inventory-Short Form). Secondary variables will be pain catastrophising (Pain Catastrophising Scale), perceived self-efficacy regarding the disease and treatment (Pain Self-Efficacy Questionnaire), and body image and perception of visible disability (Body Image Scale). Potential confounding variables will include sociodemographic variables (age and educational level), clinical variables (time on monoclonal antibody treatment and number of previous bleeds in the last 12 months) and anthropometric variables (body mass index). Expected results: It is expected that residual chronic pain will persist in patients with severe haemophilia A treated with monoclonal antibodies and tha…

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

Talk to the study team

Rubén Cuesta-Barriuso, PhD  ·  0034 985103386  ·  cuestaruben@uniovi.es

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Locations (1)

Universidad de OviedoOviedo, Principality of Asturias, SpainRecruiting

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Source record: clinicaltrials.gov/study/NCT07096349