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Utilization of 31P-Nuclear Magnetic Resonance Spectroscopy to Monitor Brain Energy Deficit in Huntington Disease (PRO-MH2)

I

Institut National de la Santé Et de la Recherche Médicale, France

Status

Completed

Conditions

Huntington Disease

Treatments

Other: 31-Phosphorus RMN Spectroscopy

Study type

Interventional

Funder types

Other

Identifiers

NCT01696708
2012-A01063-40 (Registry Identifier)
C12-49

Details and patient eligibility

About

The purpose of this project is to study brain energy profile evolution at different stages of the Huntington disease.

Enrollment

50 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • UHDRS < 50
  • Age > 18 years
  • Ability to undergo MR scanning
  • Covered by french social security

Exclusion criteria

  • Evidence of psychiatric disorder
  • Attendant neurological disorder
  • Contraindications to MRI (claustrophobia, metallic or material implants)
  • Severe head injury
  • Unable to understand the protocol
  • Pregnancy
  • Failure to give informed consent
  • Subjects with exclusion criteria required by french law (e.g. subjects who require a legally authorized representative to obtain consent)
  • Unwillingness to be informed in case of abnormal MRI

Trial design

Primary purpose

Basic Science

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

50 participants in 2 patient groups

Patients
Other group
Description:
31-Phosphorus RMN Spectroscopy
Treatment:
Other: 31-Phosphorus RMN Spectroscopy
Volunteers
Other group
Description:
31-Phosphorus RMN Spectroscopy
Treatment:
Other: 31-Phosphorus RMN Spectroscopy

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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