View Clinical Trial (Medical Research Study)
Evaluation, Treatment and Monitoring of Patients With a Known or Suspected Parasitic Infection - NCT00001645-20892(Clinical Trial 111222)
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| City: |
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Bethesda |
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State:
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MD |
| Zip Code: |
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20892 |
| Conditions: |
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Chagas Disease - Malaria - Parasitic Disease - Trypanosomiasis |
| Purpose: |
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The purpose of this study is to evaluate, treat and follow patients with parasitic
infections.
People with a known or suspected parasitic infection who are at least 1 year old may be
enrolled. This study does not involve any experimental treatments.
Participants will have a physical examination and laboratory tests on blood, stool, or
urine. Blood samples may be collected at regular intervals, but no more than 450 ml (15
ounces) of blood will be drawn from adults, and no more than 7 ml (1-1/2 teaspoons) per kg
(2.2 pounds) of body weight from children, in any 6-week period. Other tests may include
x-rays, electrocardiogram (EKG), or tissue biopsy (surgical removal of a small tissue
sample), depending on the individual's condition.
Patients may be offered treatment or may be referred to another study that is more
appropriate for the problem. Any treatment provided in this study will be according to
standard medical practice for the patient's specific medical problem. Patients' responses to
treatment will be evaluated at regularly scheduled clinic visits. The length of time between
visits and the total duration of the study for a given individual will be determined by the
study doctor, based on that person's medical condition.
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| Study summary: |
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This study is designed as a prospective study to evaluate and treat patients with parasitic
infection. Up to 500 patients with known or suspected parasitic infection will be enrolled
and will be evaluated for the presence of a parasitic infection. Minimal studies scheduled
for each visit will include a medical history, physical examination, routine laboratory
tests and specialized diagnostic procedures for possible parasitic infections. Treatment
plans will be individualized for each patient's particular condition, and the number and
length of additional visits and diagnostic evaluations will vary accordingly. Specific
treatment regimens will be in accordance with standard medical practice. |
| Criteria: |
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- INCLUSION CRITERIA:
Age 1 or over.
Access to a primary medical care provider outside of the NIH.
Ability to give written informed consent (for adults) and parental consent (for those
under 18).
Clinical evidence suggestive of a parasitic infection.
EXCLUSION CRITERIA:
Less than 1 year of age.
No evidence suggestive of a parasitic infection. |
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| Study is available at: |
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National Institutes of Health Clinical Center, 9000 Rockville Pike Bethesda, MD 20892 United States
Primary Contact: Patient Recruitment and Public Liaison Office Email: prpl@mail.cc.nih.gov Phone: (800) 411-1222 |
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If you are interested in this clinical trial please use the contact information above. If you would like to get additional information about this clinical trial please visit ClinicalTrials.gov.
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| Data Source: |
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ClinicalTrials.gov |
| Date Processed: |
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March 21, 2011 |
Modifications to
this listing: |
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above to view all information about this clinical trial. |
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