Erythrocyte Variants Clinical Trial
Official title:
Collection of Blood From Persons With Hemoglobin and Erythrocyte Polymorphisms for Laboratory Malaria Research
| Verified date | July 20, 2010 |
| Source | National Institutes of Health Clinical Center (CC) |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Observational |
This study will collect blood samples for use in laboratory studies of malaria. The World
Health Organization reports that 40 percent of the world's population is at risk for malaria,
mostly in the poorest countries. It is a serious disease caused by parasites. Each year,
300-500 million infections lead to more than a million deaths. However, there are traits in
red blood cells (erythrocyte) that protect people against malaria. In this study,
polymorphism refers to the various kinds of red blood cell traits.
The sickle cell trait is an example of one that seems to offer a natural survival advantage
in children where malaria is common. Researchers at the Laboratory of Malaria and Vector
Research are investigating ways in which the blood cell traits can offer such protection, and
new knowledge gained can bring about medical advances. Of particular importance is studying
how the malaria organism, Plasmodium, survives inside different red blood cells. A steady,
consistent, and reliable supply of fresh whole blood is necessary for testing.
Patients 18 to 65, weighing more than 110 lbs. and who do not have anemia or known HIV,
Hepatitis C, or Hepatitis B may be eligible for this study.
Patients will undergo a medical history and general assessment including vital signs of
temperature, heart rate, and blood pressure. Blood will be collected from a vein in the arm,
or rarely a vein in the hand. A complete blood count, or CBC, will be done to ensure that
blood levels are sufficient and that blood donation is safe for a patient to do. Patients
need to have enough hemoglobin, the part of red blood cells that transports oxygen throughout
the body. The blood will also be tested to confirm the type of red blood cell traits of
patients. About 1 to 8 tablespoons may be collected, but most blood samples will be small,
that is, 1 to 4 teaspoons. After the patients' first visit, sessions will take 5-20 minutes.
Blood collection will total no more than 2 cups from a donor during any 6-week period.
Although the frequency of blood donations is not known at this time, it is unlikely that a
patient will be asked to donate blood more than four times a year. It may be important for
patients to undergo a repeat CBC or tests for blood chemistry if results are needed for
research. Risks associated with blood collection are considered minimal. They include
discomfort, occasional bruising or bleeding at the puncture site, and faintness.
In this study, it is possible that a small amount of blood may be stored for future research,
to help the researchers to learn more about malaria. There are no plans for the results from
the various research laboratory tests to be made available to patients or to their private
doctors. However, patients in this study may discuss the results of routine medical tests
with the study investigators. Some of the blood collected will be tested for genetic
conditions. Through genetic testing, researchers can learn more about how health or illness
may be passed on to people by their parents, or from people to their children. All results of
tests will remain confidential. Blood samples will be labeled by code, and reference to
patients' identities will be protected.
Participants will receive $50 for each blood donation. This study will not have a direct
benefit for participants. Future research that uses their blood samples will help researchers
to learn about malaria as well as how to prevent or treat the disease.
| Status | Completed |
| Enrollment | 130 |
| Est. completion date | July 20, 2010 |
| Est. primary completion date | |
| Accepts healthy volunteers | Accepts Healthy Volunteers |
| Gender | All |
| Age group | 18 Years to 65 Years |
| Eligibility |
- INCLUSION CRITERIA: Normal volunteer or volunteer with a known or suspected erythrocyte mutation. Age greater than or equal to 18 and less than or equal to 65 years old. Weight greater than 110 pounds. Ability to sign the consent form. Willingness to comply with study procedures. EXCLUSION CRITERIA: Transfusion of any blood products within the past 90 days. Active bleeding. Clinically apparent and/or symptomatic anemia (pallor, orthostasis, etc). Self-reported history of HIV, Hepatitis B virus, or Hepatitis C virus infection. Severe chronic disease (e.g. end-stage renal failure, malignancy, etc). Significant medical history, physical examination, or laboratory test results indicating that the subject should not participate in a clinical trial. |
| Country | Name | City | State |
|---|---|---|---|
| United States | National Institutes of Health Clinical Center, 9000 Rockville Pike | Bethesda | Maryland |
| Lead Sponsor | Collaborator |
|---|---|
| National Institute of Allergy and Infectious Diseases (NIAID) |
United States,