FHHI-OI-Camelot; QME
Los Angeles, California, 90245, United States
NCT Number: NCT04349410
Diagnostic determination of disease and treatment responses has been limited to qualitative imaging, measurement of serum markers of disease, and sampling of tissue. In each of these instances, there is a built in error either due to sensitivity and specificity issues, clinician interpretation of results, or acceptance of the use of an indirect marker (blood test) of what is happening elsewhere in the body - at the tissue level.
The Fleming Method for Tissue and Vascular Differentiation and Metabolism (FMTVDM) using same state single or sequential quantification comparisons [1] provides the first and only patented test (#9566037) - along with the associated submitted patent applications ruled to be covered under #9566037 - that quantitatively measures changes in tissue resulting from inter alia a disease process. This includes inter alia coronary artery disease (CAD), cancer and infectious/inflammatory processes including CoVid-19 pneumonia (CVP) resulting from the metabolic and regional blood flow differences (RBFDs) caused by these diseases.
The purpose of this paper is to make clinicians and researchers aware of this proposed method for investigating the prevalence and severity of CVP - in addition to providing rapid determination of treatment response in each patient, directing treatment decisions; thereby reducing the loss of time, money, resources and patient lives.
Looking for future studies?
Notify MeAll sexes
Interventional
Phase 2 / Phase 3
Los Angeles, California, 90245, United States
FMTVDM - See Appendix A.
Regions-of-interest (ROIs) will drawn by the nuclear technologist - either at the bedside or in the nuclear laboratory - to provide FMTVDM measurements using software already present in the nuclear camera systems. Specific ROIs will be drawn of the right lung (total), left lung (total), mediastinum (thymus activity), and any specific areas where increased tracer uptake is noted.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
CoVid-19 -
Exclusion criteria
Decision by patient to not participate.
-
FMTVDM Planar, SPECT, PET
FMTVDM Planar, SPECT, PET
FMTVDM Planar, SPECT, PET
FMTVDM Planar, SPECT, PET
FMTVDM Planar, SPECT, PET
FMTVDM Planar, SPECT, PET
FMTVDM Planar, SPECT, PET
FMTVDM Planar, SPECT, PET
FMTVDM Planar, SPECT, PET
FMTVDM Planar, SPECT, PET
FMTVDM Planar, SPECT, PET
Time frame: 72 hours
Measured improvement in tissue as measured using FMTVDM
Time frame: 7 days
Extubation
Time frame: 30 days
Self explanatory
The Camelot Foundation
Other
Acronym: FMTVDM
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.