No intervention
OtherNo intervention
NCT Number: NCT05718986
This study investigates families with at least two cases of B-cell lymphoproliferative disorders (LPD), and evaluates the prevalence of LPD in families, the relationship between medical history, genetic factors, and the risk of familial LPD, and various clinical outcomes for these families in a multiethnic population of Jews and Arabs in Israel.
Trial opening soon.
Get Notified18 year and older
All sexes
Observational
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Patients must have LPD and must have a family history of LPD. LPD patients who signed an informed consent to participate in the study.
Criteria for the inclusion of relatives of patients:
Relatives must be related by blood to LPD patients or unrelated (for control group).
Relatives who signed an informed consent to participate in the study.
Exclusion criteria
No intervention
Time frame: 5 years
Time frame: 5 years
Time frame: 15 years
Contact information is provided by the study sponsor or research team.
Geffen Kleinstern, PhD
CONTACT
Tamar Tadmor, MD
CONTACT
University of Haifa
Other
Epidemiology of Familial B-cell Lymphoproliferative Disorders
Acronym: Familial_LPD
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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