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Clinical Trial Summary

The purpose of this research study is to test the safety and benefit of a human cord blood derived stem cell infusion as a treatment for individuals with post COVID-19 neurological problems. Participants in the study will have 6 clinic visits over a 12 to 14 mo. period with each visit lasting 2 to 6 hours. Participants will receive 1 stem cell infusion at study visit #3. Participants will have a brain PET and MRI scan at the baseline and 6mo. post-infusion visits. Follow-up safety assessments will be conducted at 6mo. and 1yr. after the stem cell infusion.


Clinical Trial Description

This is a non-randomized, Phase 1/2a dose escalation study using allogenic cord tissue MSC's in adults with chronic neurological symptoms following an acute COVID-19 infection. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06156241
Study type Interventional
Source The University of Texas Health Science Center, Houston
Contact Charles S. Cox, MD
Phone 713.500.7300
Email charles.s.cox@uth.tmc.edu
Status Not yet recruiting
Phase Phase 1
Start date January 2024
Completion date February 2026