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Clinical Trial Summary

The purpose of this study is to determine whether SMDS patients treated with NR at the proposed dose exhibit decreased glucose uptake in the aorta, to determine if NR treatment results in measurable changes of blood NAD+ and NR levels, to determine if aortic measurements are stable after treatment with NR and to evaluate the safety and tolerability of NR in SMDS patients.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06280482
Study type Interventional
Source The University of Texas Health Science Center, Houston
Contact David R Murdock, MD
Phone (713) 500-6735
Email David.R.Murdock@uth.tmc.edu
Status Recruiting
Phase Phase 1
Start date March 6, 2024
Completion date July 25, 2025