Other Clinical Trial - Neuropsychiatric Post-Acute Sequelae of SARS-CoV-2

Clinical Trial Summary

The overarching goal of this study is to develop PET/MR techniques for the diagnosis of neuropsychiatric post-acute sequelae (PASC) of SARS-CoV-2. The central hypothesis is that immunological and cerebrovascular dysfunction after acute SARS-CoV-2 infections mediate neuropsychiatric PASC (NP-PASC).

Interventional studies are often prospective and are specifically tailored to evaluate direct impacts of treatment or preventive measures on disease.

Observational studies are often retrospective and are used to assess potential causation in exposure-outcome relationships and therefore influence preventive methods.

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Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
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Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
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NCT number	NCT05615415
Study type	Observational
Source	NYU Langone Health
Contact	Steven Baete
Phone	2122634861
Email	Steven.baete@nyulangone.org
Status	Recruiting
Phase
Start date	February 15, 2022
Completion date	December 31, 2024

Neuropsychiatric Post-Acute Sequelae of SARS-CoV-2 (PASC) Using TSPO Positron Emission Tomography (PET) and MRI

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms