XXXXXX- Xenon & Neural Inertia | Clinical Research Studies Listing

Recruiting

99 years or below

All

Phase N/A

20 participants needed

1 Location

Brief description of study

This pilot study involves the administration of xenon gas via the ENHANCER 3000 delivery system to 12 healthy adult volunteers; xenon concentrations will range from 0% to up to 75%. Subjects will wear an Actiwatch for 7 days and nights prior to xenon administration (Study Day) and 7 days/nights afterwards. Subjects will also undergo neurocognitive testing. They will undergo a series of head CTs before, during, and after xenon administration. The initial CT is a full-coverage CT, but subsequent scans will be limited to 3-slice acquisitions.

Eligibility of study

You may be eligible for this study if you meet the following criteria:

Conditions: Neurocognitive Dysfunction
Age: 99 years or below
Gender: All

Updated on 19 Feb 2024. Study ID: 824229

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