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All Patients: for Coronavirus (CAPTURE-2 Trial)
N/A
Waitlist Available
Led By Vicki Kalen
Research Sponsored by LumiraDx UK Limited
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 4 months
Awards & highlights
No Placebo-Only Group
Summary
This trial evaluates how well the LumiraDx SARS-CoV-2 Ab Test works compared to the reference method.
Eligible Conditions
- Coronavirus
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 4 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~4 months
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Performance Evaluation
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
1Treatment groups
Experimental Treatment
Group I: All Patients:Experimental Treatment2 Interventions
Capillary and Venous Blood Collections
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Who is running the clinical trial?
LumiraDx UK LimitedLead Sponsor
15 Previous Clinical Trials
34,337 Total Patients Enrolled
Vicki KalenPrincipal InvestigatorEclipse Clinical Research
William SimonPrincipal InvestigatorProfessional Research Network of Kansas
2 Previous Clinical Trials
2,200 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- You are currently using or have used an experimental treatment or device in the last 30 days.
Research Study Groups:
This trial has the following groups:- Group 1: All Patients:
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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