A Normal Donor Sample Collection Study in Healthy Adults
Completed
- Conditions
- Healthy Normal Volunteers
- Registration Number
- NCT01318863
- Lead Sponsor
- Astute Medical, Inc.
- Brief Summary
More than one site will participate in the collection of blood and urine samples from healthy adult subjects. These samples will be used for future testing to serve as aged-matched normal controls and to establish normal reference ranges in the development of new invitro diagnostic devices.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 300
Inclusion Criteria
- Apparently healthy adults (age ≥ 21 years)
- Provide written informed consent for study participation
Exclusion Criteria
- Any known or suspected acute illness or condition - including acute infections - at the time of enrollment or within the previous 30 days;
- Any known or suspected significant chronic medical conditions (such as diabetes, coronary artery disease, renal insufficiency, hypertension, hypercholesterolemia, chronic inflammatory diseases [e.g., rheumatoid arthritis], cancer, etc);
- Trauma-related surgery within the last 6 months;
- Any surgery, hospitalization or institutionalization (such as in a nursing home) during the previous 3 months;
- Received any blood product transfusion within the previous 2 months;
- Pregnant women or children;
- Prisoners or institutionalized individuals;
- Already provided blood or urine samples for this study.
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (4)
Research Across America
🇺🇸Dallas, Texas, United States
Rochester Clinical Research, Inc.
🇺🇸Rochester, New York, United States
Apex Research Institute
🇺🇸Santa Ana, California, United States
Clinical Research Consortium
🇺🇸Las Vegas, Nevada, United States