Collection of Blood From Patients With Cancer

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorNational Cancer Institute (NCI)

About this trial

This study will collect blood from patients with cancer to study the level of cells which decrease the immune response (suppressor cells) before and after chemotherapy. Patients 18 years of age and older with cancer may participate. This study does not involve treatment.

Participants will have about 50 ml (3 tablespoonfuls) of blood drawn. Depending on their condition, patients may be invited to enroll in a clinical research study involving chemotherapy, radiotherapy, or surgery. Additional 40-ml blood samples may be drawn during the course of treatment.

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Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

None

Disqualifiers

None

Trial population

Primary clinical; healthy volunteers may include NIH employees

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

1,750 Participants
are grouped into 2 trial groups
Group A: Healthy Volunteers
Group B: Participants

Trial outcomes

Primary outcomes

1

Undertake genetic analysis of both prokaryotic and eukaryotic samples for advanced mutational analysis.

Undertake genetic analysis of both prokaryotic and eukaryotic samples for advanced mutational analysis.

Time frame
ongoing
2

Correlate analysis results with clinical parameters such as demographics, toxicities, and treatment outcomes.

Correlate analysis results with clinical parameters such as demographics, toxicities, and treatment outcomes.

Time frame
ongoing
3

Collection of tissue, urine, saliva, stool and blood components, which include serum, leukocytes, peripheral blood mononuclear cells (PBMC), and circulating tumor cells (cTC), of human subjects.

Analyze tissue, urine, saliva, stool and blood components, which include serum, leukocytes, peripheral blood mononuclear cells (PBMC), and circulating tumor cells (cTC), of human subjects.

Time frame
ongoing

Secondary outcomes

Other outcomes

Sponsors and contacts

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