Eligibility Module

Eligibility Module

The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.

Eligibility Module path is as follows:

Study -> Protocol Section -> Eligibility Module

Eligibility Module


Ignite Creation Date: 2025-12-24 @ 3:19 PM
Ignite Modification Date: 2025-12-24 @ 3:19 PM
NCT ID: NCT02269592
Eligibility Criteria: Inclusion Criteria: * Patients with Known or Suspected Precursor Hematological Cancer * Including the following subgroups of diseases: * Early MDS, including pathologically-confirmed MDS (IPSS Low/Int-1; IPSS-R Very Low/Low) and idiopathic cytopenias of undetermined significance (ICUS); * Asymptomatic Multiple Myeloma and Waldenstrom Macroglobulinemia such as monoclonal gammopathy of undermined significance (MGUS) or Smoldering Multiple Myeloma (SMM or SWM); * Monoclonal B cell lymphocytosis (MBL); * Early stage asymptomatic low-grade lymphomas; or * Other precursor conditions or clonal genetic abnormalities of the blood/bone marrow that do not meet criteria for symptomatic hematological malignancy, or patients exposed to prior chemotherapies (e. g., alkylating agents, platinum derivatives, taxanes, topo-2 inhibitors, anti-metabolites, systemic radioisotopes). * Patients must be at least 18 years of age to participate in this research. * Inclusion of Women and Minorities -- In accordance with NIH guidelines, women and members of minority groups and their subpopulations will be included in this protocol. Exclusion Criteria: * Patients with Known or Suspected Precursor Hematological Cancer are NOT EXCLUDED * Evidence of symptomatic or active hematological malignancy. Patients enrolled on clinical trials for precursor diseases are NOT excluded from this study.
Healthy Volunteers: False
Sex: ALL
Minimum Age: 18 Years
Study: NCT02269592
Study Brief:
Protocol Section: NCT02269592