Detecting Autologous Transfusion by Measuring Alterations in the Dynamics of Red Blood Cell Maturation and Recycling

Utah System of Higher Education (USHE) logo

Utah System of Higher Education (USHE)

Status and phase

Completed
Early Phase 1

Conditions

Blood Transfusion, Autologous
Blood Doping

Treatments

Other: Control - Normal Saline (Placebo)
Other: Autologous Transfusion

Study type

Interventional

Funder types

Other
Industry

Identifiers

NCT02684747
83533

Details and patient eligibility

About

A total of 40 subjects will be recruited for participation in this study. 20 subjects (10 males and 10 females) will be randomized to the active group (those receiving re-infusion of autologous blood) and 20 subjects (10 males and 10 females) will be randomized to the placebo group (receiving NS infusion).

Full description

Autologous blood transfusion is a major problem in a wide range of competitive sports. Methods with increased sensitivity, specificity, and feasibility are needed to identify athletes who cheat in this manner and compromise their health and the integrity of their sports in general. Complete blood counts (CBC) offer routine high-resolution assessment of the current hematologic status of individuals, providing estimates of a number of blood characteristics, such as the total hemoglobin concentration in the blood (HGB) and the volume fraction of cells in the blood (HCT). These CBC components are homeostatically controlled by the carefully regulated dynamic processes of red blood cell (RBC) production in and release from the bone marrow, RBC maturation in the peripheral circulation over the course of the ~100-day RBC lifespan, and clearance and recycling of senescent cells. Any significant perturbation to the circulating population of RBCs, like autologous transfusion, will immediately trigger compensatory modulation of one or more of these dynamic processes. The investigators believe quantification of these underlying dynamic processes will enable us to detect autologous transfusion. These dynamic RBC processes cannot currently be measured directly, but novel mathematical modeling enables their inference from routine complete blood and reticulocyte counts. The investigators propose to test the ability of modeled RBC dynamics to identify instances of autologous blood transfusion.

Enrollment

40 patients

Sex

All

Ages

18 to 35 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. Male or female between 18-35 years old
  2. Classified as low risk and will not have any major signs or symptoms suggestive of cardiovascular, pulmonary, or metabolic disease according to the American College of Sports Medicine's (ACSM) risk stratification categories
  3. The subjects should be well-trained endurance athletes. This group could consist of cyclists (road and mountain), triathletes, runners, long-distance swimmers, etc.

Exclusion criteria

  1. Age less than 18 or greater than 35 on the day of enrollment
  2. Any contraindication to blood donation as defined by the American Association of Blood Banks http://www.fda.gov/downloads/BiologicsBloodVaccines/BloodBloodProducts/QuestionsaboutBlood/UCM272981.pdf
  3. Any chronic illness (e.g.diabetes, heart disease, hypotension, anemia, hemoglobinopathy, marrow diseases, leukemia/lymphoma, pregnancy, amenorrhea/female athlete triad)
  4. Any abnormal CBC index or iron study; any blood dyscrasia
  5. Abnormal blood and urine tests for doping agents (e.g. phthalates)
  6. Positive uhCG or women who are attempting to get pregnant during the study period
  7. Unwilling or unable to provide blood samples or receive a blood transfusion
  8. Not a participant in endurance sports activities
  9. Are currently on any medications that might affect hematologic parameters including, but not restricted to, hematopoietic medications
  10. Subjects with a baseline hemoglobin above 16.7 g/dL, or baseline hematocrit below 35% or above 55%.
  11. Any subject that plans to participate in an organized athletic event (or USA Cycling sanctioned event) within 30 days following the re-infusion phase of the study will not be allowed to participate in the study

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

40 participants in 2 patient groups, including a placebo group

Treatment - Autologous Transfusion
Experimental group
Description:
Participants will be randomized to the treatment group (autologous transfusion)
Treatment:
Other: Autologous Transfusion
Control - Normal Saline (Placebo)
Placebo Comparator group
Description:
Participants will either be randomized to the control group (saline transfusion)
Treatment:
Other: Control - Normal Saline (Placebo)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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