sEV angiogenic properties in cardiovascular risk patients

Clinical Score: 0.900 Price: $0.50 type 2 diabetes, obesity, ischemic disease human patients Status: proposed

What This Experiment Tests

Clinical experiment designed to assess clinical efficacy targeting N/A in human patients. Primary outcome: sEV angiogenic capability

Description

This study evaluated the angiogenic capability of serum-derived extracellular vesicles (sEV) from different patient populations including type 2 diabetic subjects, obese individuals with and without diabetes, and subjects with ischemic disease. The research aimed to identify patients who may benefit from autologous sEV administration for pro-angiogenic therapy by comparing sEV properties across these different cardiovascular risk groups. The study involved both in-vitro and in-vivo assessment of angiogenic properties.

TARGET GENE
N/A
MODEL SYSTEM
human patients
ESTIMATED COST
$0
TIMELINE
0 months
PATHWAY
angiogenesis
SOURCE
extracted_from_pmid_31959759
PRIMARY OUTCOME
sEV angiogenic capability

Scoring Dimensions

Info Gain 0.00 (25%) Feasibility 0.00 (20%) Hyp Coverage 0.00 (20%) Cost Effect. 0.00 (15%) Novelty 0.00 (10%) Ethical Safety 0.00 (10%) 0.900 composite

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Angiogenesis Pathwaymechanism

Protocol

sEV isolation from serum, in-vitro and in-vivo angiogenic assays across patient groups

Expected Outcomes

Different angiogenic properties between patient groups, identification of predictive biomarkers

Success Criteria

Differential angiogenic capability between patient groups

Related Hypotheses (0)

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