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Outcomes of Prophylaxis and On-demand Treatment for Severe Hemophiliacs and Collection of Baseline Data in Hemophiliacs in Taiwan

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02908243
Enrollment
350
Registered
2016-09-20
Start date
2015-02-28
Completion date
2018-12-31
Last updated
2016-09-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hemophilia

Keywords

Hemophilia, Primary prophylaxis, Pettersson Score, Joint function study, Comorbidity

Brief summary

Primary prophylaxis in severe hemophiliacs is defined that prophylaxis therapy starts before 2 years of age and prior to any clinically evident joint bleeding or after first joint bleeding and prior to the onset of joint damage irrespective of age, joints can be kept normal or very mildly damaged till teenage or adulthood. Primary prophylaxis has been proved to be more beneficial and cause less damage to joint than on-demand therapy. Primary prophylaxis is also known to be able to decrease the occurrence of factor VIII inhibitor and is the most advanced and useful, cost-effective therapy for hemophilia care. However, it requires 2 to 3 injections of factor VIII or IX of 20-50 IU/Kg doses every week, it costs a lot of expenses. In the year 2013, we tried hard to discuss with Bureau of National Health Insurance (BNHI) and have meeting a couple of time, eventually a guideline of an intermediate-dose prophylaxis for severe hemophilia was established and a consensus was reached that this prophylactic treatment will be cost effective without increased burden of total budget. This guideline was finally approved by BNHI and will be implemented from July 1st, 2014. In oder to evaluate the efficacy of prophylaxis treatment, patients will be arranged to come back to each hemophilia center at least once a year to have investigation of doses and annual consumption of clotting factors, frequencies and causes of bleedings, especially joint bleedings, joint outcome by studies of hemophilia joint health score (HJHS), hemophilia actives list and health-related quality of life. These results will be collected and compared between intermediate-dose prophylaxis group of patients and on demand treatment group of patients. The life span of hemophiliacs has been improved remarkably in recent years due to sufficient and adequate treatments, especially prophylaxis treatment, therefore comorbidities in the hemophilic population, e.g. hypertension, diabetes, hyperlipidemia and cancer, etc, have been found with prevalences close to those in non-hemophilic population. It is worth that the prevalence of these comorbidity will also be investigated. In addition, basic data of the patients including age, sex, severity, the development of inhibitor and viral infection etc will also be collected for analysis.

Interventions

OTHERcollection of baseline data

collection of baseline data including ages, types, severity, inhibitors and comorbidities

Sponsors

Changhua Christian Hospital
CollaboratorOTHER
Taipei Medical University Hospital
CollaboratorOTHER
Taipei Veterans General Hospital, Taiwan
CollaboratorOTHER_GOV
Taipei Medical University Shuang Ho Hospital
CollaboratorOTHER
Taichung Veterans General Hospital
CollaboratorOTHER
China Medical University Hospital
CollaboratorOTHER
Kaohsiung Medical University Chung-Ho Memorial Hospital
CollaboratorOTHER
Taiwan Society of Thrombosis and Hemostasis
Lead SponsorOTHER

Study design

Observational model
COHORT

Eligibility

Sex/Gender
MALE
Age
2 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* all severe hemophilia A and B patients more than 2 years of age and without inhibitor

Exclusion criteria

* female hemophilia * hemophiliac patients with inhibitor \> = 0.6 Bethesda unit (BU)

Design outcomes

Primary

MeasureTime frameDescription
annual bleeding ratethrough study completion, an average of 1 yearspontaneous and traumatic joint and other site bleedings

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026