Last reviewed · How we verify

NCT04532411: HexapodBooth

COVID-19 Testing Sample Acquisition Throughput and Efficiency

Completed Last updated 23 October 2023
What this trial tests

trial testing Personal Protective Testing Booth in SARS-CoV Infection in 28,948 participants. Completed in 30 September 2020.

Timeline
1 March 2020
Primary endpoint
30 September 2020
30 September 2020

Quick facts

Lead sponsorMassachusetts General Hospital
StatusCompleted
Study typeOBSERVATIONAL
Enrollment28,948
Start date1 March 2020
Primary completion30 September 2020
Estimated completion30 September 2020
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Massachusetts General Hospital

Who can join

Eligibility, any sex, with SARS-CoV Infection or Respiratory Viral Infection. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This QI project seeks to evaluate the relative test sample acquisition throughput, personal protective equipment utilization, and relative operational costs of provider-administered COVID-19 (SARS-CoV-2) nasal samples with and with the use of HEPA-filtered, positive pressure isolation booths.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other recruiting trials for SARS-CoV Infection

Currently open trials in the same condition.

Other Massachusetts General Hospital trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04532411.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing