The EDC is live today — see what ships now
All studies
NCT00067054From ClinicalTrials.govRecruiting

Apheresis and Specimen Collection Procedures to Obtain Plasma, Peripheral Blood Mononuclear Cells (PBMCs) and Other Specimens for Research Studies

VRC 200: A Multicenter Specimen Collection Protocol to Obtain Human Biological Samples for Research Studies

  • Sample Collection

At a glance

Phase
Phase not stated
Study type
Observational
Sponsor
National Institute of Allergy and Infectious Diseases (NIAID)
Enrolment target
3,000
Started
10 September 2003
Main results due
Not stated
Study sites
3
Registry updated
28 September 2026

Can you take part?

  • Aged 3 years and over.
  • Open to any sex.
  • Healthy volunteers can take part.

These are the headline rules only. Every study has a longer list, and whether you are eligible is decided by the research team at the site — never by this page.

Read the full eligibility criteria
* INCLUSION CRITERIA FOR ADULT PARTICIPANTS:

A participant must meet all the inclusion criteria, as follows:

1. Age 18 years or older
2. Able and willing to complete the informed consent process
3. Willing to provide blood or other samples that will be stored indefinitely and used for future research
4. Able to provide proof of identity to the acceptance of the clinician completing the enrollment process; when informed consent is obtained by telephone or a telehealth visit, the investigator obtaining consent will also confirm proof of identity.

INCLUSION CRITERIA FOR CHILDREN:

1. Children aged 3 to 17 years inclusive, and at least 12 kg in weight.
2. Capability of the legal adult guardian of the child to understand and comply with the planned study procedures.
3. Capability of the legal adult guardian of the child to provide written informed consent.
4. Willing to have blood drawn or collection of urine, fecal samples, oral secretions, or swabs of mucosa that will be stored indefinitely and used for future research.
5. The legal adult guardian of the children can provide proof of identity for the child and for themselves to the satisfaction of the clinician completing the enrollment process.

EXCLUSION CRITERIA FOR ALL PARTICIPANTS:

A participant will be excluded from protocol participation if there is presence of a condition that the attending physician considers to be a contraindication to the specimen collection procedures.

EXCLUSION CRITERIA FOR CHILDREN ONLY

1. Acute or chronic illness that, in the opinion of the investigator or designee, precludes participation in the study.
2. Factors related to the legal guardian that, in the judgment of the investigator or designee, may affect the objective decision-making of the legal guardian.

SKIN BIOPSY ELIGIBILITY CRITERIA FOR ADULTS ONLY:

The skin biopsy eligibility includes the following:

1. Age 18 years or older
2. No known allergies to the local anesthetic to be used
3. No history of keloid formation
4. No known coagulation disorders
5. Not pregnant or breast feeding

APHERESIS ELIGIBILITY CRITERIA FOR ADULTS ONLY:

* To undergo an apheresis procedure, a participant must have no medical contraindications. All apheresis procedures performed under this protocol are solely for research purposes.
* Participants involved in an active clinical research protocol may participate in the apheresis protocol if the total amount of blood drawn does not exceed NIH guidelines or a site's institutional guidelines. A study clinician will complete a checklist for apheresis eligibility before referring a participant for apheresis.
* At the NIH, prior to the scheduled procedure, the participant must have a venous assessment performed by apheresis staff to determine suitability for apheresis.

For Healthy Volunteers:

A healthy volunteer must meet all the following criteria prior to the procedure:

1. Age 18 years or older
2. Afebrile (temperature \<= 37.5 degrees C)
3. Weight \>=110 pounds
4. Adequate bilateral antecubital venous access
5. Hemoglobin \>= 12.5 g/dL for women; \>= 13.0 g/dL for men within 56 days prior to apheresis procedure.
6. Platelets \> 150,000 K/uL within 56 days prior to apheresis procedure.
7. No cardiovascular instability as indicated by a) history of medically significant cardiac arrhythmia within the last 12 months, or b) ischemic cardiovascular disease within the last 12 months, or c) heart rate outside of the 50-100 beats/minute interval (on 3 successive readings), or d) blood pressure greater than 180 mmHg (systolic) or 100 mmHg (diastolic) on 3 successive readings
8. No current lung or kidney disease
9. No known coagulation disorder
10. No sickle cell disease
11. No active or chronic hepatitis
12. No intravenous injection drug use in the past 5 years
13. Not breast feeding
14. Negative beta-human chorionic gonadotropin (beta-HCG) pregnancy test (urine or serum) performed by a VRC study clinician within 72 hours prior to the apheresis procedure

Patients with an Infectious Disease:

A patient with an infectious disease must meet all the following criteria:

1. Age 18 years or older
2. Weight \>= 110 pounds
3. Afebrile (temperature \<= 37.5 degrees C)
4. Adequate bilateral antecubital venous access
5. No cardiovascular instability as indicated by a) history of medically significant cardiac arrhythmia within the last 12 months, or b) ischemic cardiovascular disease within the last 12 months, or c) heart rate outside of the 50-100 beats/minute (on 3 successive readings), or d) blood pressure greater than 180/100 mmHg (on 3 successive readings)
6. No current lung or kidney disease
7. No known coagulation disorder
8. No receipt of clotting factor concentrates in the past 5 years
9. Hemoglobin \>= 9.0 g/dL within 56 days prior to apheresis procedure
10. Platelets \>= 50,000 K/uL within 56 days prior to apheresis procedure
11. White Blood Cell (WBC) \>= 2.0 K/uL within 56 days prior to apheresis procedure
12. Not breast feeding
13. Negative beta-human chorionic gonadotropin (beta-HCG) pregnancy test (urine or serum) performed by a VRC study clinician within 72 hours prior to the apheresis procedure

What this study is about

In the sponsor’s own words, from the registry.

This study collects specimens from volunteers for use in studies by NIAID's Vaccine Research Center. A number of different types of specimens or samples can be collected, including blood, urine, body fluids or secretions, skin swabs, or skin biopsies. The samples are used for medical research, including the study of HIV, hepatitis, and other diseases; immune system responses, such as responses to vaccinations or infections; and for research on vaccine development.

Blood samples may be collected either by ordinary blood drawing (phlebotomy) or by apheresis, a procedure for collecting a larger quantity of blood cells or plasma than would be possible through simple blood drawing. For this procedure, the participant lies on a recliner or couch. Blood is removed through a needle in the vein of one arm and spun in a machine that separates out the desired component (plasma or white blood cells). The remainder of the blood is returned either through the same needle or through a needle in the other arm. The procedure takes about 1 to 3 hours.

Volunteers who are 18 years of age and older, including participants in other NIH research protocols, may be eligible. Individuals who have a condition that the research staff considers a reason not to make a sample donation will be excluded from the study.

Participants may have only one sample collected or may be asked to undergo repetitive sample collection procedures, depending upon the requirements of the particular research project for which the samples are being collected. Each individual's enrollment is for a 1-year period, which can be extended.

Study sites(3)

  • National Institutes of Health Clinical Center

    Bethesda, Maryland, United States

    Recruiting

  • EvergreenHealth Medical Center

    Kirkland, Washington, United States

    Completed

  • University of Puerto Rico Medical Sciences Campus

    San Juan, Puerto Rico

    Active, not recruiting

Showing 3 of 3 sites. 1 of the 3 sites on this study is recruiting right now — a site can stop enrolling while the study as a whole is still open.

Source: ClinicalTrials.gov record NCT00067054. Trialion does not run this study, is not paid to refer anyone to it, and cannot enrol you. Eligibility is always decided by the research team at the site.

Not the right study?

Answer three questions and see the studies recruiting near you, in plain language.

Find a study for me
Apheresis and Specimen Collection Procedures to Obtain Plasma, Peripheral Blood Mononuclear Cells (PBMCs) and | Trialion