Sample Collection From Healthy Volunteers for Assay Optimization
| Status: | Recruiting |
|---|---|
| Conditions: | Healthy Studies |
| Therapuetic Areas: | Other |
| Healthy: | No |
| Age Range: | 18 - 80 |
| Updated: | 1/17/2019 |
| Start Date: | June 28, 2018 |
| End Date: | June 30, 2027 |
| Contact: | Laura E Failla, C.R.N.P. |
| Email: | laura.failla@nih.gov |
| Phone: | (240) 669-5323 |
Background:
The Laboratory of Immune System Biology (LISB) works with other labs at the National
Institutes of Health. They study how parts of living things come together to make a whole.
LISB designs and improves research tests on human samples like blood and cells. In order to
do its work, LISB needs to have a lot of these samples available.
Objective:
To collect biological specimens to use for designing and improving research tests. Specimens
include blood, stool, saliva, and skin/mucosal swabs.
Eligibility:
Healthy people ages 18-80
Design:
Participants will be screened with an interview about their general health and their medical
history. They will have a physical exam and blood tests.
If the results of the screening are normal, participants will be asked to give one or more of
these samples:
Blood will be drawn from an arm vein with a needle and syringe.
Mucus and skin will be collected by rubbing the area with a cotton swab. The areas may
include the top of the tongue, inside the cheek, nostrils, behind the ear, elbow pit, or
vagina.
Participants will spit into a tube to collect saliva.
Participants will pass stool into a plastic container that fits in the toilet under the seat.
They will get sampling kits and instructions.
Over the next 5 years, if more samples are needed, participants will be contacted to set up
another visit to the NIH. These visits will each take about 1 hour.
About every 2 years, when participants come to NIH for a visit, extra blood will be
collected. It will be tested for HIV and hepatitis B and C.
The Laboratory of Immune System Biology (LISB) works with other labs at the National
Institutes of Health. They study how parts of living things come together to make a whole.
LISB designs and improves research tests on human samples like blood and cells. In order to
do its work, LISB needs to have a lot of these samples available.
Objective:
To collect biological specimens to use for designing and improving research tests. Specimens
include blood, stool, saliva, and skin/mucosal swabs.
Eligibility:
Healthy people ages 18-80
Design:
Participants will be screened with an interview about their general health and their medical
history. They will have a physical exam and blood tests.
If the results of the screening are normal, participants will be asked to give one or more of
these samples:
Blood will be drawn from an arm vein with a needle and syringe.
Mucus and skin will be collected by rubbing the area with a cotton swab. The areas may
include the top of the tongue, inside the cheek, nostrils, behind the ear, elbow pit, or
vagina.
Participants will spit into a tube to collect saliva.
Participants will pass stool into a plastic container that fits in the toilet under the seat.
They will get sampling kits and instructions.
Over the next 5 years, if more samples are needed, participants will be contacted to set up
another visit to the NIH. These visits will each take about 1 hour.
About every 2 years, when participants come to NIH for a visit, extra blood will be
collected. It will be tested for HIV and hepatitis B and C.
The Laboratory of Immune System Biology plays a major role in fostering the growth of systems
biology efforts across the National Institutes of Health, in large measure through its
development of new tools for high-throughput data generation and complex systems modeling.
The lab's experimental component requires ongoing assay development and optimization, which
depend on the availability of human biological samples for testing. The primary purpose of
this protocol is to obtain biological specimens from healthy volunteers to support the lab s
development and optimization of scientific assays and to use as control samples for research
tests in other studies.The secondary objective of this study is to track immunologic changes
over time using the assays developed and optimized in this study.
biology efforts across the National Institutes of Health, in large measure through its
development of new tools for high-throughput data generation and complex systems modeling.
The lab's experimental component requires ongoing assay development and optimization, which
depend on the availability of human biological samples for testing. The primary purpose of
this protocol is to obtain biological specimens from healthy volunteers to support the lab s
development and optimization of scientific assays and to use as control samples for research
tests in other studies.The secondary objective of this study is to track immunologic changes
over time using the assays developed and optimized in this study.
- INCLUSION CRITERIA:
1. Age 18-80 years.
2. Able to provide informed consent.
3. Agree to allow biological samples to be stored for future research.
4. Willing to provide blood, stool, saliva, and/or skin/mucosal swabs.
EXCLUSION CRITERIA:
1. Pregnancy.
2. History of autoimmune or autoinflammatory disease.
3. Diabetes mellitus.
4. Cancer chemotherapy within the past 5 years.
5. Currently receiving treatment for an active malignancy.
6. Surgery within the past 8 weeks.
7. History of recent (within the past 30 days) infection.
8. History of parasitic, amebic, fungal or mycobacterial infections within the past 5
years.
9. Infected with HIV and/or hepatitis B and/or C.
10. Use of an oral glucocorticoid within the past 30 days.
11. History of a bleeding disorder.
12. Complete blood count with differential and/or acute care panel values are both outside
of the NIH Department of Laboratory Medicine normal reference range and deemed
clinically significant by the principal investigator (PI).
13. Receipt of an immunosuppressant or immunomodulatory drug within the past 30 days.
14. Receipt of a live-attenuated vaccine within the past 30 days.
15. Receipt of any other type of vaccine within the past 14 days.
16. Current or past use (within the past 90 days) of immunoglobulin therapy.
17. Current use of illicit drugs (per subject report).
18. Current use of nicotine-containing products, including cigarettes and chewing tobacco,
nicotine patches, gum, electronic cigarettes, etc.
19. Current alcohol use disorders (criteria per Diagnostic and Statistical Manual of
Mental Disorders, fifth edition).
20. Any condition that requires active medical intervention or monitoring to avert serious
danger to the individual s health or wellbeing.
21. Any condition that, in the opinion of the PI, contraindicates participation in this
study.
Co-enrollment guidelines: Participants may be co-enrolled in other studies with the
approval of the PI.
We found this trial at
1
site
9000 Rockville Pike
Bethesda, Maryland 20892
Bethesda, Maryland 20892
301-496-2563
Phone: 800-411-1222
National Institutes of Health Clinical Center The National Institutes of Health (NIH) Clinical Center in...
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