Transfusion of Biotin-Labeled Red Blood Cells
Status: | Recruiting |
---|---|
Conditions: | Healthy Studies |
Therapuetic Areas: | Other |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 3/22/2019 |
Start Date: | April 28, 2019 |
End Date: | December 2024 |
Contact: | Nicole Helbling, RN, BSN, MS |
Email: | nlr8@pitt.edu |
Phone: | 412-692-2285 |
Transfusion of Biotin-Labeled Red Blood Cells for the Evaluation of Genetic Factors That Contribute to Donor Differences in Red Blood Cell Storage and Post-Transfusion Red Blood Cell Recovery
The purpose of this research is to evaluate the impact of genetic and biologic factors in
blood donors on red blood cell storage stability after autologous transfusion over the
different range of storage period of 5-7 days and 35-42 days in healthy volunteers.
blood donors on red blood cell storage stability after autologous transfusion over the
different range of storage period of 5-7 days and 35-42 days in healthy volunteers.
Inclusion Criteria:
- Ages 18 years and older
- Weight ≥110 lbs
- Hemoglobin ≥ 12.5 g/dL or hematocrit ≥ 38% for women and hemoglobin ≥ 13.0 g/dL or
hematocrit ≥ 39% for men.
- Meet criteria for autologous blood donation
Exclusion Criteria:
- Subjects with a past medical history or symptoms of blood dyscrasia, diabetes
mellitus, hyperlipidemia, obstructive sleep apnea, renal disease, congestive heart
failure, significant cardiac disease and / or known peripheral arterial disease.
- Moderate to severe systemic hypertension (systolic blood pressure >140 mmHg and/or
diastolic blood pressure > 95 mmHg
- Systolic blood pressure <100 mmHg and/or diastolic blood pressure < 60 mmHg on the
study day.
- Positive Direct Antiglobulin Test
- Consumption of biotin supplements or raw eggs within 30 days
- Treatment with antibiotics in the week before initiating study participation to avoid
suppression of erythropoiesis, which may accompany infection.
- Blood loss in the previous 8 weeks due to epistaxis, trauma, hemoptysis,
gastrointestinal bleeding, diagnostic phlebotomy (> 30 ml)
- Subjects who report tobacco or marijuana smoking within 6 months of study.
- Cognitively impaired subjects, or institutionalized persons and subjects unable or
unwilling to complete written informed consent
- Subjects with a history of blood donation within the last 56 days.
- Use of other investigational drugs/devices within 30 days of screening.
- Subjects taking any medication for the treatment of diabetes including insulin
- Females of childbearing potential who are pregnant or unwilling to undergo pregnancy
testing; females with positive pregnancy testing on screening day will be excluded.
- History of prior transfusion reaction to blood products.
- Allergic reaction to biotin
We found this trial at
1
site
4200 Fifth Ave
Pittsburgh, Pennsylvania 15260
Pittsburgh, Pennsylvania 15260
(412) 624-4141
Phone: 412-692-2285
University of Pittsburgh The University of Pittsburgh is a state-related research university, founded as the...
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