CTRI/2014/03/004494Active, not recruiting未知
Assessment of the effectiveness of prophylactic replacement of lower than ââ?¬Ë?standardââ?¬â?¢ doses of clotting factor concentrates in children with severe hemophilia A - MUSFIH-PRO
BAYER AWARD0 sites30 target enrollmentStarted: TBDLast updated:
Trial Snapshot
- Phase
- 未知
- Status
- Active, not recruiting
- Sponsor
- Enrollment
- 30
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
Inclusion Criteria
- •1. Severe hemophilia, defined as factor assay showing <1% activity, between 3-7 years of age
- •2. No single joint should have an HJHS score of more than 5.
- •3. Not have detectable inhibitors by Bethesda assay ( <0.6 BU) at recruitment
- •4. Be willing to come for evaluation once in 9-15 months for at least 2 (?4) years. (in case
- •the study is extended)
Exclusion Criteria
- •PATIENTS WITH DOCUMENTED INHIBITORS.
- •NOT WILLING TO COME FOR FOLLOW UP FOR LONG TERM (ATLEAST 4 YEARS)
Investigators
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