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Clinical Trial Summary

The Vendys II, an FDA-approved device, uses finger digital thermal monitoring (DTM) after a period of blood flow restriction to evaluate vascular health. This study will evaluate the feasibility of using this device to measure the Vascular Reactivity Index (VRI) in children and adolescents/young adults (AYA) undergoing hematopoietic cell transplantation (HCT).


Clinical Trial Description

Primary Objective: -Assess the feasibility of the use of VENDYS-II in children and AYA as a measure of vascular endothelial function, where feasibility is defined as completion of the evaluation by at least 70% of consented participants. Secondary Objective: -Summarize the incidence of any adverse events that precludes completion of assessment of endothelium-dependent vasodilation using the Vendys II in children and AYA. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05029752
Study type Interventional
Source M.D. Anderson Cancer Center
Contact Kris Mahadeo
Phone (713) 792-2873
Email [email protected]
Status Recruiting
Phase N/A
Start date June 30, 2021
Completion date January 31, 2023

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