Defining the Molecular Risk in Israeli Patients With Secondary Compared to Primary Myelofibrosis
NCT03402399 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 222
Last updated 2019-07-05
Summary
The aim of the study is to determine the rate of HMR mutations in PMF and secondary MF (post PV/ET) subjects, and correlate the rate of mutations with clinical features as known prognostic scores.
Conditions
- Myelofibrosis, Primary
- Myelofibrosis, Post PV
- Myelofibrosis, Post ET
Interventions
- OTHER
-
Molecular analysis
Blood test
Sponsors & Collaborators
-
Assaf-Harofeh Medical Center
lead OTHER_GOV
Principal Investigators
-
Maya Koren-Michowitz, MD · Assaf-Harofeh Medical Center
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- OTHER
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2017-12-10
- Primary Completion
- 2019-12-09
- Completion
- 2020-12-09
Countries
- Israel
Study Locations
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