Study of a Large Family With Congenital Mirror Movements : From Underlying Pathophysiology to Culprit Gene Identification PROJET " MOMIC "
NCT ID: NCT01075061
Last Updated: 2025-08-27
Study Results
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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COMPLETED
NA
40 participants
INTERVENTIONAL
2010-02-28
2011-07-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NON_RANDOMIZED
PARALLEL
BASIC_SCIENCE
NONE
Study Groups
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healthy volunteers
healthy volunteers
healthy volunteers
morphological and functional brain MRI; transcranial magnetic stimulation
Kallmann
Kallmann syndrome patients
Kallmann
morphological and functional brain MRI; transcranial magnetic stimulation
Congenital Mirror Movement
patients with CMM
Congenital Mirror Movement
morphological and functional brain MRI; transcranial magnetic stimulation
Interventions
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healthy volunteers
morphological and functional brain MRI; transcranial magnetic stimulation
Kallmann
morphological and functional brain MRI; transcranial magnetic stimulation
Congenital Mirror Movement
morphological and functional brain MRI; transcranial magnetic stimulation
Eligibility Criteria
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Inclusion Criteria
* Members of the family of interest displaying mirror movements or being obligatory asymptomatic carrier, without additional manifestation or malformation; or patient with genetically proven Kallmann syndrome and mirror movements.
* No contraindication for MRI or TMS study
Exclusion Criteria
* Simultaneous participation in another clinical trial
* Treatment that modulate cortical excitability (for the TMS part of the study only)
11 Years
82 Years
ALL
Yes
Sponsors
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Institut National de la Santé Et de la Recherche Médicale, France
OTHER_GOV
Responsible Party
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Principal Investigators
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Emmanuel ROZE, MD
Role: PRINCIPAL_INVESTIGATOR
Institut National de la Santé Et de la Recherche Médicale, France
Locations
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Fédération des Maladies du Système Nerveux, Hôpital Pitié Salpétrière
Paris, , France
Countries
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References
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Depienne C, Cincotta M, Billot S, Bouteiller D, Groppa S, Brochard V, Flamand C, Hubsch C, Meunier S, Giovannelli F, Klebe S, Corvol JC, Vidailhet M, Brice A, Roze E. A novel DCC mutation and genetic heterogeneity in congenital mirror movements. Neurology. 2011 Jan 18;76(3):260-4. doi: 10.1212/WNL.0b013e318207b1e0.
Other Identifiers
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2009-A00490-57
Identifier Type: REGISTRY
Identifier Source: secondary_id
C09-06
Identifier Type: -
Identifier Source: org_study_id
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