Using DNA-Typing and Erythrocyte Microparticle Analysis to Detect Blood Doping

NCT03548766 · Status: UNKNOWN · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 12

Last updated 2020-08-11

No results posted yet for this study

Summary

A total of 12 subjects will be recruited for participation in this study. 6 subjects will receive re-infusion of autologous blood, and 6 subjects (anemic patients) will receive a homologous transfusion.

Conditions

  • Blood Disease
  • Blood Transfusion, Autologous
  • Blood Doping
  • Blood Transfusion, Homologous

Interventions

BIOLOGICAL

Homologous Blood Transfusion

Homologous, or allogenic, blood transfusions involves someone collecting and infusing the blood of a compatible donor into him/herself.

BIOLOGICAL

Autologous Blood Transfusion

Autologous blood transfusion is the collection and re-infusion of the patient's own blood or blood components.

Sponsors & Collaborators

  • World Anti-Doping Agency

    collaborator OTHER
  • Anti-Doping Lab Qatar

    collaborator UNKNOWN
  • Sidra Medicine

    collaborator OTHER
  • Laboratorio Antidoping FMSI

    collaborator UNKNOWN
  • Hamad Medical Corporation

    lead INDUSTRY

Principal Investigators

  • Sven Voss · ADLQ

  • Mohamed Yassin · Hamad Medical Corporation

  • Francesco Donati · Laboratorio Antidoping FMSI, Rome, Italy

  • Costas Georgakopoulos · ADLQ

  • Mohammed Alsayrafi · ADLQ

  • Jean-Charles Grivel · Sidra Medicine

  • Christophe Raynaud · Sidra Medicine

Study Design

Allocation
NON_RANDOMIZED
Purpose
DIAGNOSTIC
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
20 Years
Max Age
50 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2018-09-20
Primary Completion
2021-12-31
Completion
2021-12-31

Countries

  • Qatar

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03548766 on ClinicalTrials.gov