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MGUS clinical trials

View clinical trials related to MGUS.

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NCT ID: NCT02566265 Completed - Multiple Myeloma Clinical Trials

Study of High-dose Influenza Vaccine Efficacy by Repeated Dosing IN Gammopathy Patients

SHIVERING 2
Start date: September 2015
Phase: Phase 2
Study type: Interventional

The investigators' hypothesis is that the administration of Fluzone® High-Dose with booster to all patients with monoclonal gammopathies (irrespective of age) will lead to seroconversion rates exceeding 50% and more importantly, will reduce influenza-related morbidity, reduce interruptions in cancer therapy and may reduce disease progression at the end of the flu season

NCT ID: NCT01139476 Completed - Multiple Myeloma Clinical Trials

Specimen Collection for Agricultural Health Study Cohort Pesticide Exposure Study

Start date: June 15, 2010
Phase:
Study type: Observational

Background: - Multiple myeloma (MM), a type of cancer that affects the white blood cells, is often preceded by a precancerous disorder known as monoclonal gammopathy of undetermined significance (MGUS). Farmers and other agricultural workers have a higher risk of developing MGUS and MM, possibly because of their exposure to certain pesticides. Researchers are interested in studying biological specimens taken from participants in the Agricultural Health Study - specifically, pesticide applicators at least 50 years of age who do not have cancer- to better understand the development of MGUS and MM. Objectives: - To collect biological specimens from Agricultural Health Study participants for further research. - To examine the relationship between pesticide exposure and MGUS/MM. Eligibility: - Male pesticide applicators who are over 50 years of age, cancer-free, and participating in the Agricultural Health Study. Design: - Two groups of participants will complete the study: a general group and a smaller group of individuals who have been exposed to the pesticide diazinon. - All participants will receive an initial contact letter with information about the study, followed by a phone call to administer a screening questionnaire and arrange a home visit from a researcher within the next month. - Participants will receive by mail a urine specimen kit that will be collected at the home visit. - During the home visit, a study researcher will take blood samples and collect the urine sample, and will administer another questionnaire. - Participants in the group exposed to diazinon will have three home visits for the study: (1) prior to pesticide exposure, (2) the day after participants stop using diazinon, and (3) about 21 days after the second visit. The first visit will take place in the off-season from January to March; the second and third visits will be conducted between April and August. - No treatment will be provided as part of this study.