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
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
More Related Trials
-
Comparison of Prophylaxis and On-demand Treatment in Children With Moderate to Severe Hemophilia A
NCT02362581 ·Status: COMPLETED ·Phase: NA
-
Prophylaxis Versus on Demand Treatment for Children With Hemophilia A
NCT01810666 ·Status: COMPLETED ·Phase: PHASE4
-
A Study to Evaluate Impact of Efanesoctocog Alfa on Long-term Joint Health in Participants With Hemophilia A in Taiwan
NCT06684314 ·Status: RECRUITING
-
TGA (Thrombin Generation Assay) and Prophylaxis in Haemophilia
NCT02781766 ·Status: UNKNOWN ·Phase: NA
-
Determinants and Consequences of the Transition to Adulthood Among Adolescents With Haemophilia
NCT02866526 ·Status: COMPLETED
-
Individually Tailored Prophylaxis in Patients With Severe Hemophilia A
NCT00995046 ·Status: TERMINATED ·Phase: NA
-
Evaluate Efficacy and Safety of Recombinant Factor VIII (rFVIII)Treatment of Severe or Moderately Severe Hemophilia A
NCT02930317 ·Status: UNKNOWN ·Phase: PHASE3
-
Post Marketing Surveillance To Observe Safety And Efficacy Of Xyntha® In Subjects With Hemophilia A
NCT01790828 ·Status: COMPLETED
-
BAY14-2222 Prophylaxis and Joint Function Improvement (Adults)
NCT00586521 ·Status: COMPLETED ·Phase: PHASE4
-
A Study on the Bone-health Effectiveness of Applying Recombinant Factor VIII Fc (rFVIIIFc) to Patients With Hemophilia A (Prototype A)
NCT05981274 ·Status: RECRUITING
-
Joint Outcome Study
NCT00207597 ·Status: COMPLETED
-
The Effect of Patient Counseling on Adolescent Hemophilia Patient Compliance With Bleeding Logs
NCT00212459 ·Status: COMPLETED ·Phase: NA
-
Prophylaxis Versus On-demand Therapy Through Economic Report
NCT01159587 ·Status: COMPLETED
-
Individualized Prophylaxis for Severe Hemophilia A Children
NCT02116855 ·Status: UNKNOWN ·Phase: NA
-
Quality of Life and Adjustment Among Siblings of Children and Adolescents With Severe Hemophilia
NCT03299699 ·Status: COMPLETED
-
The Effectiveness of Recombinant Coagulation Factor IX With Recombinant Albumin (rIX-FP) in Severe Hemophilia B Patients
NCT04108260 ·Status: UNKNOWN ·Phase: PHASE4
-
2-cohort Study of Adult Patients With Severe Hemophilia A in Greece
NCT02319070 ·Status: COMPLETED
-
Post-marketing Surveillance (Special Use-results Surveillance) on Treatment With Alhemo
NCT06831734 ·Status: ENROLLING_BY_INVITATION
-
Exit Interviews to Assess Impact of Infusion Frequency in Hemophilia A
NCT02971930 ·Status: COMPLETED
-
Comparing the Burden of Illness of Hemophilia in the Developing and the Developed World
NCT01217255 ·Status: COMPLETED
-
Patient Functioning and Well-being, Economic, and Clinical Impact of Hemophilia A and Its Treatment
NCT02396862 ·Status: COMPLETED
-
Clinical and Health-related Outcome of rFVIIIFc Prophylaxis
NCT04583930 ·Status: UNKNOWN
-
Efficacy and Safety of ADVATE Standard Prophylaxis to Hemophilia A
NCT02280265 ·Status: UNKNOWN ·Phase: NA
-
Extension at 10 Years of the: "Observational Study Evaluating Efficacy and Costs of Secondary Prophylaxis vs On-demand Therapy With Kogenate Bayer in Patients With Severe Haemophilia A."
NCT02581969 ·Status: COMPLETED
-
Once-A-Day Prophylaxis for Youth and Young Adults With Severe Hemophilia A
NCT00717626 ·Status: COMPLETED ·Phase: PHASE2