Stony Brook, NYNCT05762302Now EnrollingIRB Ready

Lower Respiratory Tract Infection Clinical Trial in Stony Brook, NY

Access cutting-edge lower respiratory tract infection treatment through this clinical trial at a research site in Stony Brook. Study-provided care at no cost to qualified participants.

Sponsored by MeMed Diagnostics Ltd.

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Expert Care in Stony Brook

Access lower respiratory tract infection specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related lower respiratory tract infection treatment provided free

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Check if you qualify for this lower respiratory tract infection clinical trial in Stony Brook, NY

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Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to Stony Brook

    Convenient for NY residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Stony Brook site if eligible
  4. 4Begin participation

About This Lower Respiratory Tract Infection Study in Stony Brook

This is a Prospective, multi-center study enrolling adults subjects presented to the ED/Urgent care, with symptoms consistent with lower respiratory infection (LRTI). The reason of this study is to demonstrate the MeMed BV can help clinicians make decisions about using antibiotics in patients with lower respiratory track infections and see how it would impact clinical outcomes, antibiotics use, hospitalizations, ED clinicians find ways to improve health and medical care.

Sponsor: MeMed Diagnostics Ltd.

Who Can Participate

Inclusion Criteria

Patients eligible for inclusion are required to fulfill all of the following criteria:
Written informed consent must be obtained from the patient or his/her legal guardian.
18 years of age or older.
Current disease duration ≤ 7 days.
Tactile fever or measured temperature ≥ 37.8°C (100°F) (any body site, any measurement device, including self-reported), either of them noted at least once within the last 7 days.
Clinical suspicion of bacterial or viral LRTI: At least one of the following respiratory signs or symptoms: cough (new or worsening), sputum production, dyspnea/shortness of breath, auscultatory abnormality (e.g. wheezing, rhonchi).
Clinician intent to prescribe antibiotics based on the currently available data.

Exclusion Criteria

Patients fulfilling any of the following criteria are not eligible for inclusion in the infectious cohort:
Systemic antibiotics within 72 hours prior to enrollment
Inflammatory disease (e.g., IBD, SLE, Rheumatoid arthritis, Kawasaki, other vasculitis)
Congenital immune deficiency (CID)
A proven or suspected infection on presentation with Mycobacterial (e.g., MAC, MABC), parasitic or fungal (e.g., Candida, Histoplasma, Aspergillus) pathogen
HIV, HBV, or HCV infection (self-declared or known from medical records)
Major surgery, trauma and\\or burns in the last 7 days
Pregnancy- self reported or medically confirmed
Active malignancy - Cancer diagnosed within the previous six months, recurrent, regionally advanced or metastatic cancer, cancer for which treatment had been administered within six months, or hematological cancer that is not in complete remission.
Patients with severe illnesses that affect life expectancy and quality of life such as end stage renal disease, end stage liver disease or severe COPD.
Clinician intent to hospitalize patient.
Patients with suspected concomitant infections (e.g. UTI, cellulitis, gastroenteritis, etc.)
Active treatment with immune-suppressive or immune-modulating therapies, including without limitations: Administration of PO\\IV\\IM high dose steroids \>1mg/kg/day prednisone (or equivalent) at some point in the past 10 days or daily continuous use of steroids \> 0.25 mg/kg/day in the past 7 days Monoclonal antibodies, anti-TNF agents Intravenous immunoglobulin (IVIG) Cyclosporine, Cyclophosphamide, Tacrolimus, Azathioprine, Methotrexate G/GM-CSF, Interferons •Considered unsuitable for the study by the study team

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Stony Brook?

Yes, this clinical trial (NCT05762302) has an active research site in Stony Brook, NY that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Lower Respiratory Tract Infection Treatment Options in Stony Brook, NY

If you're searching for lower respiratory tract infection treatment options in Stony Brook, NY, this clinical trial (NCT05762302) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Stony Brook research site is actively enrolling participants for this clinical trial. You'll receive care from experienced lower respiratory tract infection specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all lower respiratory tract infection clinical trials near you to find additional studies recruiting in your area.

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