Skip to content

Evaluating the Analytical Equivalency of Serum and Whole Blood Samples Run on the MeMed Key® Platform (Perseverance Study)

A Prospective Multi-center Sample Collection Study for Evaluating the Analytical Equivalency of Serum and Whole Blood Samples Run on the MeMed Key® Platform (Perseverance Study)

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05439551
Enrollment
215
Registered
2022-06-30
Start date
2022-02-11
Completion date
2023-09-29
Last updated
2023-10-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Infection

Brief summary

This is a Prospective, multi-center, sample collection study enrolling pediatric and adult subjects presented to the ED/Urgent care, with symptoms consistent with acute bacterial or viral infection will be recruited according to eligibility criteria. The study is designed to measure the MeMed BV®️ score in whole blood and serum samples and demonstrate the equivalence between the two matrices. Patients will be managed according to the current standard of care per standard institutional procedures.

Interventions

DIAGNOSTIC_TESTMeMed BV®

Patients Serum and Whole blood samples will be examined using the MeMed BV® test. Test results will have no impact on patient management.

Sponsors

MeMed Diagnostics Ltd.
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
90 Days to No maximum
Healthy volunteers
No

Inclusion criteria

1. Written informed consent must be obtained from the patient or his/her legal guardian. For children under 18 years old, written informed consent from the legal guardian must be obtained and assent from the patient may be required depending on the local requirements. 2. Over 90 days of age. 3. Clinical suspicion of acute bacterial or viral infection. 4. Symptoms of acute infectious disease \< 7 days. 5. Experienced fever at least once within the last 7 days (self-reported or Temperature ≥ 37.8°C (100°F)).

Exclusion criteria

1. HIV, HBV, active HCV, or active Tuberculosis infection (self-declared or known from medical records). 2. Suspicion and/or confirmed diagnosis of infectious gastroenteritis/ colitis. 3. Active inflammatory disease (e.g., IBD, SLE, JIA, RA, Kawasaki, other vasculitis). 4. Pregnancy- self reported or medically confirmed. 5. Active malignancy. 6. Congenital or acquired immune deficiency (CID). 7. A proven or suspected infection on presentation with Mycobacterial (e.g., Tuberculosis, MAC), parasitic or fungal (e.g., Candida, Histoplasma, Aspergillus) pathogen. 8. Significant trauma or burns in the last 7 days. 9. Patients that have undergone major surgery in the last 7 days. 10. Current treatment with immune-suppressive or immune-modulating therapies, including without limitations: 1. Administration of P.O.\\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 2. Monoclonal antibodies, anti-TNF agents 3. Intravenous immunoglobulin (IVIG) 4. Cyclosporine, Cyclophosphamide, Tacrolimus, Azathioprine, Methotrexate 5. G/GM-CSF, Interferons.

Design outcomes

Primary

MeasureTime frame
Measuring the MeMed BV® score with whole blood and serum samples from patients suspected of acute bacterial or viral infection and demonstrating the equivalence between the two matrices.Through study completion, an average of 18 months

Countries

Israel, United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026