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Diagnostic Test
Swab for Respiratory Syncytial Virus (INSPIRE Trial)
N/A
Recruiting
Led By Robert Rosen
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
INSPIRE Trial Summary
This trial looked at how well the LumiraDx test works for Influenza A/B and RSV at various point of care testing sites.
Eligible Conditions
- Respiratory Syncytial Virus
- Flu
INSPIRE Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 4 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~4 months
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Performance evaluation by health care professionals
Performance evaluation by non-laboratory users
INSPIRE Trial Design
2Treatment groups
Experimental Treatment
Group I: Nasopharyngeal swabExperimental Treatment1 Intervention
Nasopharyngeal swab from subjects with signs and symptoms of influenza and/or RSV-like illness
Group II: Nasal swabExperimental Treatment1 Intervention
Nasal swab from subjects with signs and symptoms of influenza and/or RSV-like illness
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Swab
2019
N/A
~100
Find a Location
Who is running the clinical trial?
LumiraDx UK LimitedLead Sponsor
15 Previous Clinical Trials
32,490 Total Patients Enrolled
Robert RosenPrincipal InvestigatorArdmore Family Practice
1 Previous Clinical Trials
1,134 Total Patients Enrolled
Andre GvozdenPrincipal InvestigatorGvozden Pediatrics
1 Previous Clinical Trials
1,134 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:Research Study Groups:
This trial has the following groups:- Group 1: Nasopharyngeal swab
- Group 2: Nasal swab
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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