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NCT06816953: HEADUS_SHA8

Cartilage Biomarkers and HEAD-US Score in Severe Hemophilia A Patients Receiving FVIII Prophylaxis

ENROLLING BY INVITATION NA Last updated 10 February 2025
What this trial tests

NA trial testing HEAD-US in Hemophilia A in 19 participants. Enrolling by invitation.

Timeline
1 April 2024
Primary endpoint
30 January 2025
28 February 2025

Quick facts

Lead sponsorChulalongkorn University
PhaseNA
StatusENROLLING BY INVITATION
Study typeINTERVENTIONAL
Allocationnon randomized
Designsequential
Maskingnone
Primary purposetreatment
Enrollment19
Start date1 April 2024
Primary completion30 January 2025
Estimated completion28 February 2025
Sites1 location across Thailand

Drugs / interventions tested

Conditions studied

Sponsor

Chulalongkorn University

Who can join

Eligibility, any sex, with Hemophilia A. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Patients with severe hemophilia A often develop joint complication requiring careful monitoring. This study aimed to compare the effectiveness of standard low dose weight-based FVIII concentrates (CFCs) prophylaxis with pharmacokinetic-guided extended half-life FVIII concentrates (eHLFVIII) using cartilage biomarkers and HEAD-US score.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Hemophilia A

Currently open trials in the same condition.

Other Chulalongkorn University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06816953.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing