Safety evaluation study for patients with polycythemia vera
Phase 1
Recruiting
- Conditions
- Polycythemia VeraMyeloproliferative Neoplasms
- Registration Number
- JPRN-jRCT2051210083
- Lead Sponsor
- Ito Tomoki
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 6
Inclusion Criteria
1. Confirmed diagnosis of PV according to either the 2008 or 2016 WHO classification criteria
2. PV patients being only treated with phlebotomy and the interval is 4-9 weeks
Exclusion Criteria
Patients administrated drugs for PV treatment such as hydroxyurea or ruxolitinib (aspirin is excluded)
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method