Surgiscreen Registration

NCT01589133 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 3109

Last updated 2013-05-30

No results posted yet for this study

Summary

The purpose of this study is to assess the consistency of the results of irregular antibody screening with Surgiscreen (investigational reagent) and Serascan Diana 3 (control reagent), and the consistency of the results of irregular antibody screening with investigational reagent on serum and plasma from same patients.

Conditions

  • Irregular Antibody Screening

Sponsors & Collaborators

  • Johnson & Johnson Medical, China

    lead INDUSTRY

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-05-31
Primary Completion
2012-10-31
Completion
2012-10-31

Countries

  • China

Study Locations

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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 NCT01589133 on ClinicalTrials.gov