RECRUITING

Bioaerosol Sampling Device (BSD) Clinical Study

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The goal of this clinical trial is to learn about the bioaerosol sampling device (BSD) and how it can sample patient bioaerosols (breath) and patient's nares for the detection of COVID-19 viral particles in patients seeking to be tested for COVID-19.

Official Title

BIOAEROSOL SAMPLING DEVICE (BSD) CLINICAL STUDY: Performance of Respiratory Pathogen Bioaerosol Sampling Device Compared to Matched Swab Sample With Molecular and Antigen Assays That Can Detect SARS-CoV-2 Phase II Validation

Quick Facts

Study Start:2023-07-10
Study Completion:2024-05-19
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06047067

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:5 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:CHILD, ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. Age 18 years or older
  2. Willing and able to provide informed consent
  3. Able to understand and follow study procedures
  4. Stable medical condition
  1. Pregnancy or breastfeeding
  2. Severe psychiatric disorders
  3. Active substance abuse
  4. Unstable medical conditions
  5. Inability to comply with study requirements

Contacts and Locations

Study Contact

Study Cooridnator
CONTACT
(619) 635-5843
emerald@cantorbioconnect.com

Principal Investigator

Robert Azurin, MD
PRINCIPAL_INVESTIGATOR
JPRA Enterprises, LLC

Study Locations (Sites)

JPRA Enterprise, LLC
S. Gate, California, 90280
United States
Alfa Medical Research
Hollywood, Florida, 33204
United States
Alfa Medical Urgent Care
Pembroke Pines, Florida, 33029
United States
HDH Research
Houston, Texas, 77009
United States
HDH Research
Houston, Texas, 77022
United States
HDH Research
Humble, Texas, 77338
United States

Collaborators and Investigators

Sponsor: Cantor BioConnect, Inc.

  • Robert Azurin, MD, PRINCIPAL_INVESTIGATOR, JPRA Enterprises, LLC

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2023-07-10
Study Completion Date2024-05-19

Study Record Updates

Study Start Date2023-07-10
Study Completion Date2024-05-19

Terms related to this study

Keywords Provided by Researchers

  • COVID-19
  • Rapid diagnostic test
  • SARS-CoV-2
  • SARS-CoV-1

Additional Relevant MeSH Terms

  • COVID-19