Health Condition 1: null- Breast, Colorectal, Lung, Cervix Uteri, Prostate, Stomach and Head & Neck Cancer
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Written informed consent. 2. Confirmed diagnosis of stage 2-4 breast, lung, colorectal cervix uteri, prostate, stomach and head & neck cancer, (OR) no prior history of cancer. 3. Stage 2-4 treatment naive, metastatic, secondary, and recurrent cancer patients. 4. Able to undergo blood collection prior to initiation of chemotherapy treatment, (OR) able to provide blood sample if subject is a non-cancer control subject.
Exclusion criteria
Exclusion criteria: 1. Patients unable to understand the research protocol and/or provide informed consent. 2. Patients with known immunodeficiency, or pregnancy.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The number of circulating tumor cells (CTCs) per milliliter of whole blood. Reported unit of measure will be the number of CTCs/milliliter. Timepoint: Blood samples will be collected from study subjects at a single timepoint and analyzed for the number of circulating tumor cells (CTCs) within 7 days (168 Hrs) of blood collection. | — |
Secondary
| Measure | Time frame |
|---|---|
| Not ApplicableTimepoint: Not Applicable | — |
Countries
India
Contacts
Actorius Innovations and Research Pvt Ltd