Quantitative T1rho Magnetic Resonance Imaging in Healthy Subjects

NCT ID: NCT04993196

Last Updated: 2024-08-21

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

30 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-08-01

Study Completion Date

2025-06-01

Brief Summary

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T1rho imaging is a new MRI technique that has strong potential in neuroimaging. This technique does not require exogenous contrast agents and has high spatial resolution.

In this study we aim to characterise the normal appearance of T1rho in the brain parenchyma in healthy participants. T1rho values will be measured in normal brain structures.

Detailed Description

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Conditions

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Magnetic Resonance Imaging

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

NONE

Study Groups

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T1rho MRI

Group Type EXPERIMENTAL

T1rho imaging

Intervention Type DIAGNOSTIC_TEST

Magnetic Resonance Imaging using T1rho

Interventions

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T1rho imaging

Magnetic Resonance Imaging using T1rho

Intervention Type DIAGNOSTIC_TEST

Eligibility Criteria

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Inclusion Criteria

\- Male and female volunteers greater than or equal to 18 years of age

Exclusion Criteria

* Subjects with a contraindication to magnetic resonance imaging such as the presence of metallic implants, claustrophobia and pregnancy.
* Subjects with previous severe allergic or anaphylactoid reaction to a gadolinium contrast agent, or contraindication to contrast gadolinium administration, such severe renal disease or acutely deteriorating renal function, who would be at risk of nephrogenic systemic fibrosis
* Subjects who are unable to tolerate the scan without moving the head as a result of symptoms such as tremor, spasticity, involuntary movements and spasms, cognitive impairment, coughing, and shortness of breath.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Chinese University of Hong Kong

OTHER

Sponsor Role lead

Responsible Party

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Professor Tiffany So

Clinical Assistant Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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CUHK

Hong Kong, , Hong Kong

Site Status RECRUITING

Countries

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Hong Kong

Central Contacts

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Tiffany So

Role: CONTACT

+85235051035

Facility Contacts

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Tiffany So

Role: primary

Other Identifiers

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TSo

Identifier Type: -

Identifier Source: org_study_id

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