Inherited Movement DisordersBIOMOVNCT05034172
Biomarker Research in Inherited Movement Disorders
An observational study of Inherited Movement Disorders and Spinocerebellar Ataxias, run by Assistance Publique - Hôpitaux de Paris at 1 site in France.
Trial summary
Inherited movement disorders are rare conditions, whose cumulative prevalence are in the order of 5-10/100,000 inhabitants, in most cases progressive and can lead to a significant loss of autonomy after one or more decades of evolution. Read more about this study
- Who is it for?
- Ages 7 years and olderHealthy volunteers can take part
- Conditions the study is for
- Inherited Movement Disorders, Spinocerebellar Ataxias, Hyperkinetic Disorders
- What is being tested?
- Clinical follow-up
- How many people
- 4,000 participants
- Where
- 1 siteFrance
- Study dates
- 25 Aug 2021to 25 Aug 2031
- Phase
- Observational
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 7 years and older
- All sexes
- Healthy volunteers accepted
- Child, Adult, Older adult
Study population: * Patients with hyperkinetic movement disorders * At risk individuals (gene mutation carriers) with inherited hyperkinetic movement disorders * Healthy controls to allow variant classification and establish normal values for scales
Who may be able to join
- Common inclusion criteria for all participants:
- - Affiliated with a social security system or beneficiary of such a regime
- Group of patients:
- Any patient with inherited hyperkinetic movement disorders can be included in the study according to the following criteria:
- Woman or man;
- Clinical diagnosis of inherited hyperkinetic movement disorders with or without a genetic diagnosis
Show all 25Show fewer
- With or without familial history of the disease
- Age ≥ 7 years;
- Signed Informed consent by the patient or both of holders of the parental authority for minors, or by the le;gal guardian for adults under guardianship
- Group of at-risk individuals:
- Woman or man;
- Age ≥ 18 years old;
- A first-degree relative of a patient with inherited hyperkinetic movement disorders
- OR a carrier of an identified pathogenic variant or expansion in one of the pathological gene variant involved in one of these diseases;
- Normal neurological examination; according to disease specific scales
- Signed Informed consent by the subject or by the legal guardian for adults under guardianship
- Group of healthy controls:
- Woman or man;
- Aged ≥ 18 years old;
- Free of known neurological pathology;
- No significant neurological symptoms;
- Signed Informed consent by the subject
- Common inclusion criteria for elective participant for skin biopsy (optional): - Age ≥10 ans
- Ability to undergo a skin biopsy
- Common inclusion criteria for elective participant for MRI examination (optional): - Ability to undergo a MRI.
Who cannot join
- Absolute criteria for non-inclusion for all groups:
- Person deprived of their liberty by judicial decision
- Contra-indications to MRI examination (optional): metallic implant, pacemaker, artificial heart valve, brain vascular malformation, aneurysm clips, exposed by metallic fragments, artificial implants, peripheral or neuronal stimulator, insulin pump, intravenous catheter, epilepsy, metallic contraceptive device, claustrophobia,
- Contra-indication to skin biopsy (optional):
- Taking anticoagulant or antiplatelet medication (see above),
- History of hemostasis disorders,
- Presence of hemorrhagic risk verified by a coagulation test
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
France1 site, 1 recruiting
- Recruiting
Hôpital Pitié Salpetrière
Paris, 75013
Alexandra DURR, PUPH, 1.57.27.46.94 ext. +33, alexandra.durr@icm-institute.org
Mariana Atencio, 1.57.27.46.94 ext. +33, mariana.atencio@icm-institute.org
About this study
Inherited movement disorders are rare conditions, whose cumulative prevalence are in the order of 5-10/100,000 inhabitants, in most cases progressive and can lead to a significant loss of autonomy after one or more decades of evolution. They include spinocerebellar ataxias and hyperkinetic disorders (dystonias, choreas, tremor, parkinsonism and myoclonus with variable combination of those, or more complex alteration of movements). The existence of the National Reference Centre (CMR) for Rare Diseases (CMR Neurogenetics, devoted to ataxias and spastic paraparesis, dystonia and rare movement disorders and CMR Huntington, devoted to Huntington Disease) has allowed a more integrated vision of these diseases. This is illustrated, in the same family, by the occurrence of different clinical expressions of spinocerebellar ataxias and hyperkinetic disorders that share the same genetic background. Conversely, different causal mutations within the same gene may have very different ages at onset and a wide range of clinical expression, and the spectrum of new phenotypes linked to a single gene is still expanding . Many ataxia and dystonia genes are involved in similar pathways. There are numerous arguments supporting a share pathogenesis including synaptic transmission and neurodevelopment .
BIOMOV project aims to :
- establish the clinical spectrum and natural history of these diseases,
- understand the role of genetic and familial factors on the phenotype,
- elucidate the molecular basis of these disorders and evaluate diagnostic strategies involving molecular tools for clinical and genetic management,
- develop multimodal biomarkers both for physiopathological studies and for accurate measures of disease progression,
- develop trial ready cohorts of well characterized genetic patients,
- test new therapies either symptomatic or based on pathophysiological mechanisms.
Read the detailed description
Inherited movement disorders are rare conditions, whose cumulative prevalence are in the order of 5-10/100,000 inhabitants, in most cases progressive and can lead to a significant loss of autonomy after one or more decades of evolution. They include spinocerebellar ataxias and hyperkinetic disorders (dystonias, choreas, tremor, parkinsonism and myoclonus with variable combination of those, or more complex alteration of movements). The existence of the National Reference Centre (CMR) for Rare Diseases (CMR Neurogenetics, devoted to ataxias and spastic paraparesis, dystonia and rare movement disorders and CMR Huntington, devoted to Huntington Disease) has allowed a more integrated vision of these diseases. This is illustrated, in the same family, by the occurrence of different clinical expressions of spinocerebellar ataxias and hyperkinetic disorders that share the same genetic background. Conversely, different causal mutations within the same gene may have very different ages at onset and a wide range of clinical expression, and the spectrum of new phenotypes linked to a single gene is still expanding .
any ataxia and dystonia genes are involved in similar pathways. There are numerous arguments supporting a share pathogenesis including synaptic transmission and neurodevelopment .
Overall, there are a number of arguments for a shared genetic approach and biomarkers research for these inherited movement disorders:
- Evidence from a clinico-genetic approach: A combination of several movement disorders is often observed in the same patient with causative mutation in either genetic groups of spinocerebellar degenerations, dystonias or choreas.
- Evidence from neuroimaging: the current concept of networks disorders underlies the pathophysiology of these hyperkinetic movement disorders. Variable combination of functional and/ or structural alterations of the cerebello-thalamo-cortical, cortex-basal ganglia and corticospinal networks, and their complex interactions have been described in ataxias ,dystonia choreas and more complex disorders.
- Genetic diagnosis: deciphering diagnosis with wide range of phenotypes Even in times of next generation sequencing covering exomes and genomes, diagnosing spinocerebellar degenerations, dystonia and other hyperkinetic disorders remains a challenge as: i) the causative gene remains to be identified for a substantial share those disorders; the pathogenicity of variants of unknown significance in known and potential novel disease genes often requires time-consuming functional analyses not available on a routine basis; ii) in many countries, including France, access to diagnostic whole exome and whole genome sequencing is still limited; iii) the proportions of abnormal expansions not seen in exome studies are frequent in spinocerebellar degenerations and need a technological development to identify them. Analysis of familial forms revealed a great heterogeneity of the phenotype within the same family in terms of age at onset, severity and clinical presentation. Moreover, this phenotypic variability is not explained only by the genetic heterogeneity but also by the underlying frequent exonic or intronic expansions of triplet or more complex repeats, and more recently by the discovery of genetic modifiers ; iv) for dystonia and hyperkinetic disorders, some of those disorders also include nonmovement disorders neurological (e.g. intellectual deficiencies, hypotonia at birth, immature motor control, deafness, visual defects) and non-neurological (dysmorphological features) symptoms and the movement disorders panels do not always include the genes involved in developmental disorders; v) among the dominantly inherited forms such as Huntington disease, the access to genetic testing procedures allows early preventive therapeutic interventions in premanifest individuals. There is a lack of clinical evaluation to tackle the efficiency of treatment and the need for biomarker development.
- Natural history and prognosis: need for quantitative, reproducible markers, sensitive to evolution Biomarkers search is ongoing in those pathologies. They are valuable in assisting diagnosis, have prognostic value, quantify disease progression and serve as outcome parameters in clinical trials.
These elements demonstrate the need to develop quantitative tools that are easy to use, reproducible and sensitive to disease progression in order to accurately determine the natural history of the disease. This lack of systematic knowledge impedes diagnosis, patient counselling and therapy development.
Overall: Identification of the underlying gene and its pathogenic changes or variant(s) contributes to precise diagnosis, genetic counselling and follow-up. Advances in molecular genetics have highlighted the genotypic complexity, justifying the need for rigorous clinical and para-clinical evaluation to establish relevant phenotype-genotype correlations. In dystonia and in spinocerebellar degenerations attempts have been made to classify the genes involved.
Molecular genetic analysis will make it possible to specify the correlations between phenotype and genotype in order to propose rational molecular diagnostic strategies based on the frequency and nature of mutations, taking into account the phenotype. Genetic analyses will have an impact in terms of public health since they will serve as a basis for guiding requests for molecular analyses in these pathologies. In addition, recent advances in therapeutic trials will need the careful selection of participants, mostly based on biomarkers, for successful testing of new therapeutical agents. Therefore, it seems essential that this cohort of patients be supplemented by a collection of biological material for genetic research.
BIOMOV project aims to : 1) establish the clinical spectrum and natural history of these diseases, 2) understand the role of genetic and familial factors on the phenotype, 3) elucidate the molecular basis of these disorders and evaluate diagnostic strategies involving molecular tools for clinical and genetic management, 4) develop multimodal biomarkers both for physiopathological studies and for accurate measures of disease progression, 5) develop trial ready cohorts of well characterized genetic patients, 6) test new therapies either symptomatic or based on pathophysiological mechanisms.
It is crucial to be able to establish a large cohort of patients whose genotype will be specified. Follow-up of patients at different stages of the disease will make it possible to collect the natural history of the disease in a descriptive manner, with prospects for patient management, since the prognosis in terms of loss of autonomy or disability will be better specified. However, the main interest of the proposed clinical follow-up is to be able to quantitatively describe the progression of the main neurological diseases. These data are absolutely essential for the future implementation of therapeutic trials. The number of patients likely to be recruited and followed up a unique resource for such a project
- Being tested
- Clinical follow-up
- Medical subject headings
- Spinocerebellar Ataxias, Attention Deficit Disorder with Hyperactivity
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Clinical follow-upOther
Clinical Follow-up:
demographic data and history,
- Retrospective interview (collection of data useful for genetic studies): -disease history (for patients only);
- Family history - Neurological examination:
- Diagnosis Clinical examination;
- Rating scales specific to the pathology under investigation;
- Cerebral MRI (optional)
- Biological samples (optional)
What is being measured
The primary outcome is the main question the study is designed to answer.
Genetic entities among rare movement disorders: Pathology characterization (clinical spectrum) and its natural history: clinical Biomarkers
Comparison of clinical biomarkers at different disease stages compared to controls.
Measured: 10 years
Genetic entities among rare movement disorders: Pathology characterization (clinical spectrum) and its natural history : genetic Biomarkers
Comparison of genetic biomarkers at different disease stages compared to controls.
Measured: 10 years
Genetic entities among rare movement disorders: Pathology characterization (clinical spectrum) and its natural history : biological and/or imaging Biomarkers
Comparison of biological and/or imaging biomarkers at different disease stages compared to controls.
Measured: 10 years
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted5 Sep 2021
- Study start25 Aug 2021
- Primary completion25 Aug 2031 (estimated)
- Study completion25 Aug 2031 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Inherited Movement DisordersStudies of the same condition, open and under way.
- More trials run by Assistance Publique - Hôpitaux de ParisThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 4,000 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Assistance Publique - Hôpitaux de Paris
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05034172
- Sponsor's protocol ID
- APHP210069
- Acronym
- BIOMOV
- Status last verified
- Apr 2024
- First submitted
- 17 Jun 2021
- Last updated
- 12 Apr 2024
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 12 Apr 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Biomarker Research in Inherited Movement Disorders
- ClinicalTrials.gov ID
- NCT05034172
- Acronym / sponsor ID
- BIOMOV / APHP210069
- Study type
- Observational
- Recruitment status
- Recruiting
- Enrolment
- 4,000 participants (estimated)
- Lead sponsor
- Assistance Publique - Hôpitaux de ParisUniversity, hospital or other
- Study start
- 25 Aug 2021 (actual)
- Primary completion
- 25 Aug 2031 (estimated)
- Study completion
- 25 Aug 2031 (estimated)
- First posted
- 5 Sep 2021 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Inherited movement disorders are rare conditions, whose cumulative prevalence are in the order of 5-10/100,000 inhabitants, in most cases progressive and can lead to a significant loss of autonomy after one or more decades of evolution. They include spinocerebellar ataxias and hyperkinetic disorders (dystonias, choreas, tremor, parkinsonism and myoclonus with variable combination of those, or more complex alteration of movements). The existence of the National Reference Centre (CMR) for Rare Diseases (CMR Neurogenetics, devoted to ataxias and spastic paraparesis, dystonia and rare movement disorders and CMR Huntington, devoted to Huntington Disease) has allowed a more integrated vision of these diseases. This is illustrated, in the same family, by the occurrence of different clinical expressions of spinocerebellar ataxias and hyperkinetic disorders that share the same genetic background. Conversely, different causal mutations within the same gene may have very different ages at onset and a wide range of clinical expression, and the spectrum of new phenotypes linked to a single gene is still expanding . Many ataxia and dystonia genes are involved in similar pathways. There are numerous arguments supporting a share pathogenesis including synaptic transmission and neurodevelopment .
BIOMOV project aims to :
- establish the clinical spectrum and natural history of these diseases,
- understand the role of genetic and familial factors on the phenotype,
- elucidate the molecular basis of these disorders and evaluate diagnostic strategies involving molecular tools for clinical and genetic management,
- develop multimodal biomarkers both for physiopathological studies and for accurate measures of disease progression,
- develop trial ready cohorts of well characterized genetic patients,
- test new therapies either symptomatic or based on pathophysiological mechanisms.
Detailed description
Inherited movement disorders are rare conditions, whose cumulative prevalence are in the order of 5-10/100,000 inhabitants, in most cases progressive and can lead to a significant loss of autonomy after one or more decades of evolution. They include spinocerebellar ataxias and hyperkinetic disorders (dystonias, choreas, tremor, parkinsonism and myoclonus with variable combination of those, or more complex alteration of movements). The existence of the National Reference Centre (CMR) for Rare Diseases (CMR Neurogenetics, devoted to ataxias and spastic paraparesis, dystonia and rare movement disorders and CMR Huntington, devoted to Huntington Disease) has allowed a more integrated vision of these diseases. This is illustrated, in the same family, by the occurrence of different clinical expressions of spinocerebellar ataxias and hyperkinetic disorders that share the same genetic background. Conversely, different causal mutations within the same gene may have very different ages at onset and a wide range of clinical expression, and the spectrum of new phenotypes linked to a single gene is still expanding .
any ataxia and dystonia genes are involved in similar pathways. There are numerous arguments supporting a share pathogenesis including synaptic transmission and neurodevelopment .
Overall, there are a number of arguments for a shared genetic approach and biomarkers research for these inherited movement disorders:
- Evidence from a clinico-genetic approach: A combination of several movement disorders is often observed in the same patient with causative mutation in either genetic groups of spinocerebellar degenerations, dystonias or choreas.
- Evidence from neuroimaging: the current concept of networks disorders underlies the pathophysiology of these hyperkinetic movement disorders. Variable combination of functional and/ or structural alterations of the cerebello-thalamo-cortical, cortex-basal ganglia and corticospinal networks, and their complex interactions have been described in ataxias ,dystonia choreas and more complex disorders.
- Genetic diagnosis: deciphering diagnosis with wide range of phenotypes Even in times of next generation sequencing covering exomes and genomes, diagnosing spinocerebellar degenerations, dystonia and other hyperkinetic disorders remains a challenge as: i) the causative gene remains to be identified for a substantial share those disorders; the pathogenicity of variants of unknown significance in known and potential novel disease genes often requires time-consuming functional analyses not available on a routine basis; ii) in many countries, including France, access to diagnostic whole exome and whole genome sequencing is still limited; iii) the proportions of abnormal expansions not seen in exome studies are frequent in spinocerebellar degenerations and need a technological development to identify them. Analysis of familial forms revealed a great heterogeneity of the phenotype within the same family in terms of age at onset, severity and clinical presentation. Moreover, this phenotypic variability is not explained only by the genetic heterogeneity but also by the underlying frequent exonic or intronic expansions of triplet or more complex repeats, and more recently by the discovery of genetic modifiers ; iv) for dystonia and hyperkinetic disorders, some of those disorders also include nonmovement disorders neurological (e.g. intellectual deficiencies, hypotonia at birth, immature motor control, deafness, visual defects) and non-neurological (dysmorphological features) symptoms and the movement disorders panels do not always include the genes involved in developmental disorders; v) among the dominantly inherited forms such as Huntington disease, the access to genetic testing procedures allows early preventive therapeutic interventions in premanifest individuals. There is a lack of clinical evaluation to tackle the efficiency of treatment and the need for biomarker development.
- Natural history and prognosis: need for quantitative, reproducible markers, sensitive to evolution Biomarkers search is ongoing in those pathologies. They are valuable in assisting diagnosis, have prognostic value, quantify disease progression and serve as outcome parameters in clinical trials.
These elements demonstrate the need to develop quantitative tools that are easy to use, reproducible and sensitive to disease progression in order to accurately determine the natural history of the disease. This lack of systematic knowledge impedes diagnosis, patient counselling and therapy development.
Overall: Identification of the underlying gene and its pathogenic changes or variant(s) contributes to precise diagnosis, genetic counselling and follow-up. Advances in molecular genetics have highlighted the genotypic complexity, justifying the need for rigorous clinical and para-clinical evaluation to establish relevant phenotype-genotype correlations. In dystonia and in spinocerebellar degenerations attempts have been made to classify the genes involved.
Molecular genetic analysis will make it possible to specify the correlations between phenotype and genotype in order to propose rational molecular diagnostic strategies based on the frequency and nature of mutations, taking into account the phenotype. Genetic analyses will have an impact in terms of public health since they will serve as a basis for guiding requests for molecular analyses in these pathologies. In addition, recent advances in therapeutic trials will need the careful selection of participants, mostly based on biomarkers, for successful testing of new therapeutical agents. Therefore, it seems essential that this cohort of patients be supplemented by a collection of biological material for genetic research.
BIOMOV project aims to : 1) establish the clinical spectrum and natural history of these diseases, 2) understand the role of genetic and familial factors on the phenotype, 3) elucidate the molecular basis of these disorders and evaluate diagnostic strategies involving molecular tools for clinical and genetic management, 4) develop multimodal biomarkers both for physiopathological studies and for accurate measures of disease progression, 5) develop trial ready cohorts of well characterized genetic patients, 6) test new therapies either symptomatic or based on pathophysiological mechanisms.
It is crucial to be able to establish a large cohort of patients whose genotype will be specified. Follow-up of patients at different stages of the disease will make it possible to collect the natural history of the disease in a descriptive manner, with prospects for patient management, since the prognosis in terms of loss of autonomy or disability will be better specified. However, the main interest of the proposed clinical follow-up is to be able to quantitatively describe the progression of the main neurological diseases. These data are absolutely essential for the future implementation of therapeutic trials. The number of patients likely to be recruited and followed up a unique resource for such a project
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
Who may qualify
- Ages
- 7 years and older
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Child, Adult, Older adult
- Study population
- * Patients with hyperkinetic movement disorders * At risk individuals (gene mutation carriers) with inherited hyperkinetic movement disorders * Healthy controls to allow variant classification and establish normal values for scales
Key inclusion criteria (25 listed)
- - Affiliated with a social security system or beneficiary of such a regime
- Any patient with inherited hyperkinetic movement disorders can be included in the study according to the following criteria:
- Woman or man;
- Clinical diagnosis of inherited hyperkinetic movement disorders with or without a genetic diagnosis
- With or without familial history of the disease
Key exclusion criteria (7 listed)
- Person deprived of their liberty by judicial decision
- Contra-indications to MRI examination (optional): metallic implant, pacemaker, artificial heart valve, brain vascular malformation, aneurysm clips, exposed by metallic fragments, artificial implants, peripheral or neuronal stimulator, insulin pump, intravenous catheter, epilepsy, metallic contraceptive device, claustrophobia,
- Taking anticoagulant or antiplatelet medication (see above),
- History of hemostasis disorders,
- Presence of hemorrhagic risk verified by a coagulation test
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Clinical follow-upClinical Follow-up: demographic data and history, * Retrospective interview (collection of data useful for genetic studies): -disease history (for patients only); * Family history - Neurological examination: * Diagnosis Clinical examination; * Rating scales specific to the pathology under investigation; * Cerebral MRI (optional) * Biological samples (optional) | Other | – |
Primary outcome
Genetic entities among rare movement disorders: Pathology characterization (clinical spectrum) and its natural history: clinical Biomarkers
Time frame: 10 years
Comparison of clinical biomarkers at different disease stages compared to controls.
Genetic entities among rare movement disorders: Pathology characterization (clinical spectrum) and its natural history : genetic Biomarkers
Time frame: 10 years
Comparison of genetic biomarkers at different disease stages compared to controls.
Genetic entities among rare movement disorders: Pathology characterization (clinical spectrum) and its natural history : biological and/or imaging Biomarkers
Time frame: 10 years
Comparison of biological and/or imaging biomarkers at different disease stages compared to controls.
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 12 Apr 2024.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Inherited Movement Disorders and Spinocerebellar Ataxias, run by Assistance Publique - Hôpitaux de Paris at 1 site in France.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 25 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 12 Apr 2024. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in France. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Alexandra DURR, PUPH (142161347 ext. +33, alexandra.durr@aphp.fr), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Genetic entities among rare movement disorders: Pathology characterization (clinical spectrum) and its natural history: clinical Biomarkers (time frame: 10 years). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 12 Apr 2024.