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31P-MRS and Huntington Disease

31Phosphorus-Magnetic Resonance Spectroscopy and Huntington Disease

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01359774
Acronym
PRO-MH
Enrollment
30
Registered
2011-05-25
Start date
2011-04-30
Completion date
2012-04-30
Last updated
2025-08-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Huntington Disease

Keywords

Energy, Metabolism, Spectroscopy

Brief summary

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

Interventions

OTHER31P-MR spectroscopy

Brain energy deficit is quantified using 31P-MR spectroscopy

OTHER31P-RMN spectroscopy

Brain energy deficit is quantified using 31P-RMN spectroscopy

Sponsors

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

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
Brain energy deficit in Huntington patientsone year31P-MRS allows quantification of high-energy phosphate metabolites such as ATP and phosphocreatine. Objective: to look at brain energy metabolism during rest and activation.

Secondary

MeasureTime frameDescription
Correlating a brain energy deficit with (i) biochemical parameters and (ii) clinical parameters in Huntington patientsone yearBiochemical parameters include metabolites that we previously showed to be biomarkers in HD: branched chain amino acids and IGF1. Clinical parameters include UHDRS and TFC.

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026