Actively Recruiting

Phase 1
Age: 18Years +
All Genders
Healthy Volunteers
NCT07513532

The Primary Purpose of This Study is to Determine if Biotin, Vitamin B7 is an Effective Way to Label Platelets in Survival and Recovery Studies.

Led by Bloodworks · Updated on 2026-04-30

12

Participants Needed

1

Research Sites

34 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This is a platelet transfusion study. The primary purpose of this study is to determine if Biotin, vitamin B7 is an effective way to label platelets in survival and recovery studies. This study involves using a radioactive material as well as Biotin added to platelets to track platelets in the blood. The platelets will be collected using an apheresis procedure, labeled with biotin, and stored for 3 days. After the storage period, a radioactive material will be added to a small amount of the stored biotin-treated platelets. The radiolabeled platelets will be given back to donor and follow-up blood draws will be done to see how many of the platelets are circulating.

CONDITIONS

Official Title

The Primary Purpose of This Study is to Determine if Biotin, Vitamin B7 is an Effective Way to Label Platelets in Survival and Recovery Studies.

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Normal health status
  • Meet Bloodworks Northwest guidelines for autologous apheresis platelet donation
  • Screening chemistry and hematology lab results within normal limits
  • Negative blood donor screening panel for HIV, Hepatitis B, and Hepatitis C
  • Agreeable to birth control measures during the study
Not Eligible

You will not qualify if you...

  • Presence of clinically significant acute or chronic disease
  • Pregnant or lactating females
  • Participation in a clinical research study within 30 days before platelet collection
  • Treatment with aspirin-containing medications within 7 days before platelet collection
  • Treatment with platelet-inhibiting medications within 14 days before platelet collection
  • Splenectomized donor
  • Presence of anti-biotin or antiplatelet antibody at screening

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Bloodworks Northwest Research Institute

Seattle, Washington, United States, 98102

Actively Recruiting

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How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

BASIC_SCIENCE

Number of Arms

1

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