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31P-MRS and Huntington Disease (PRO-MH)

I

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

Status

Completed

Conditions

Huntington Disease

Treatments

Other: 31P-MR spectroscopy
Other: 31P-RMN spectroscopy

Study type

Interventional

Funder types

Other

Identifiers

NCT01359774
2011-A00137-34 (Registry Identifier)
C10-56

Details and patient eligibility

About

The purpose of this study is to identify and quantify a brain energy deficit in Huntington patients, using 31P-RMN spectroscopy.

Enrollment

30 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • 5<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

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

30 participants in 2 patient groups

Healthy volunteers
Other group
Treatment:
Other: 31P-MR spectroscopy
Huntington patients
Other group
Treatment:
Other: 31P-RMN spectroscopy

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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