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

NCT02908243 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 350

Last updated 2016-09-20

No results posted yet for this study

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.

Conditions

Interventions

OTHER

collection of baseline data

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

Sponsors & Collaborators

  • Changhua Christian Hospital

    collaborator OTHER
  • Taipei Medical University Hospital

    collaborator OTHER
  • Taipei Veterans General Hospital, Taiwan

    collaborator OTHER_GOV
  • Taipei Medical University Shuang Ho Hospital

    collaborator OTHER
  • Taichung Veterans General Hospital

    collaborator OTHER
  • China Medical University Hospital

    collaborator OTHER
  • Kaohsiung Medical University Chung-Ho Memorial Hospital

    collaborator OTHER
  • Taiwan Society of Thrombosis and Hemostasis

    lead OTHER

Principal Investigators

  • Ming-Ching Shen, BS · Changhua Christian Hospital, Changhua, Taiwan

Eligibility

Min Age
2 Years
Max Age
80 Years
Sex
MALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-02-28
Primary Completion
2018-12-31
Completion
2018-12-31

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02908243 on ClinicalTrials.gov