Viewing Study NCT02424669


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Study NCT ID: NCT02424669
Status: UNKNOWN
Last Update Posted: 2015-11-17
First Post: 2015-04-20
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Neuroinflammation in Amyotrophic Lateral Sclerosis - Mechanisms and Therapeutic Perspectives: a Translational Pilot Study Among ALS Patients
Sponsor:
Organization:

Raw JSON

{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}, 'conditionBrowseModule': {'meshes': [{'id': 'D000690', 'term': 'Amyotrophic Lateral Sclerosis'}], 'ancestors': [{'id': 'D013118', 'term': 'Spinal Cord Diseases'}, {'id': 'D002493', 'term': 'Central Nervous System Diseases'}, {'id': 'D009422', 'term': 'Nervous System Diseases'}, {'id': 'D016472', 'term': 'Motor Neuron Disease'}, {'id': 'D019636', 'term': 'Neurodegenerative Diseases'}, {'id': 'D057177', 'term': 'TDP-43 Proteinopathies'}, {'id': 'D009468', 'term': 'Neuromuscular Diseases'}, {'id': 'D057165', 'term': 'Proteostasis Deficiencies'}, {'id': 'D008659', 'term': 'Metabolic Diseases'}, {'id': 'D009750', 'term': 'Nutritional and Metabolic Diseases'}]}, 'interventionBrowseModule': {'meshes': [{'id': 'D001800', 'term': 'Blood Specimen Collection'}], 'ancestors': [{'id': 'D013048', 'term': 'Specimen Handling'}, {'id': 'D019411', 'term': 'Clinical Laboratory Techniques'}, {'id': 'D019937', 'term': 'Diagnostic Techniques and Procedures'}, {'id': 'D003933', 'term': 'Diagnosis'}, {'id': 'D011677', 'term': 'Punctures'}, {'id': 'D013514', 'term': 'Surgical Procedures, Operative'}, {'id': 'D008919', 'term': 'Investigative Techniques'}]}}, 'protocolSection': {'designModule': {'phases': ['NA'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'allocation': 'NON_RANDOMIZED', 'maskingInfo': {'masking': 'NONE'}, 'interventionModel': 'PARALLEL'}, 'enrollmentInfo': {'type': 'ESTIMATED', 'count': 100}}, 'statusModule': {'overallStatus': 'UNKNOWN', 'lastKnownStatus': 'RECRUITING', 'startDateStruct': {'date': '2015-05'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2015-11', 'completionDateStruct': {'date': '2018-11', 'type': 'ESTIMATED'}, 'lastUpdateSubmitDate': '2015-11-16', 'studyFirstSubmitDate': '2015-04-20', 'studyFirstSubmitQcDate': '2015-04-20', 'lastUpdatePostDateStruct': {'date': '2015-11-17', 'type': 'ESTIMATED'}, 'studyFirstPostDateStruct': {'date': '2015-04-23', 'type': 'ESTIMATED'}, 'primaryCompletionDateStruct': {'date': '2017-11', 'type': 'ESTIMATED'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'ALS Functional rating Scale-revised (ALS FRS-R) score', 'timeFrame': '12 months'}]}, 'conditionsModule': {'conditions': ['Amyotrophic Lateral Sclerosis (ALS)']}, 'descriptionModule': {'briefSummary': 'Amyotrophic Lateral Sclerosis (ALS) is the most common motor neuron diseases. It is considered as a rare disease with a prevalence of about 8 per 100,000 persons. Initiating in mid-life by progressive paralysis, it evolves rapidly into a generalized muscle wasting that leads irrevocably to death within 2 or 5 years of clinical onset.\n\nSince there is no cure for ALS, the management of the disease is supportive and palliative. Riluzole is the only drug that has been shown to extend survival by about three months. The identification of biomarkers sensitive to the progression of the disease might enhance the diagnostic and provide new drug targets.\n\nDysfunction of the immune system is a pathological hallmark of ALS. Increased levels of interferon gamma (IFNgamma) were found in the serum and cerebrospinal fluid (CSF) of ALS patients. However, the cell origin as well as the pathogenic influence of this peripheral source of IFNg is unknown. Thus, IFNgamma might have a role in the pathogenic process of ALS and might be a potential biomarker of the disease.'}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['ADULT', 'OLDER_ADULT'], 'maximumAge': '80 Years', 'minimumAge': '18 Years', 'healthyVolunteers': False, 'eligibilityCriteria': 'Inclusion Criteria:\n\nGroup 1 and Group 2:\n\n* with sporadic ALS (without family history), recently diagnosed (onset of first symptoms \\< 24 months) group 1, not recently diagnosed (onset of first symptoms \\> 24 months) group 2\n* Who meet the laboratory-supported probable, probable or definite form of ALS according to the El Escorial criteria\n* Suffering from the spinal form of ALS\n\nGroup 3:\n\n\\- with an inflammatory peripheral neuropathy, or a non inflammatory peripheral neuropathy, recently diagnosed\n\nExclusion Criteria:\n\n* Familial form of ALS\n* Bulbar form and respiratory onset form of ALS\n* Subjects with a clinically significant history of unstable or severe cardiac, oncologic, hepatic or renal disease, or other medically significant illness.\n* Subjects with significant cognitive impairment, clinical dementia, or psychiatric illness.\n* Female of childbearing potential (apart of patient using adequate contraceptive measures), pregnant or breast feeding\n* Suspected inability to complete the study follow-up (foreign workers, transient visitors, tourists or any others for whom follow-up evaluation is not assured)\n* Participation in any other clinical study within 30 days prior to the Screening Visit\n* Persons deprived of freedom by judicial or administrative decision, hospitalized without their consent or for other reasons than the research, under legal protection or unable to express their consent'}, 'identificationModule': {'nctId': 'NCT02424669', 'briefTitle': 'Neuroinflammation in Amyotrophic Lateral Sclerosis - Mechanisms and Therapeutic Perspectives: a Translational Pilot Study Among ALS Patients', 'organization': {'class': 'OTHER', 'fullName': 'Assistance Publique Hopitaux De Marseille'}, 'officialTitle': 'Neuroinflammation in Amyotrophic Lateral Sclerosis - Mechanisms and Therapeutic Perspectives: a Translational Pilot Study Among ALS Patients', 'orgStudyIdInfo': {'id': '2014-19'}, 'secondaryIdInfos': [{'id': 'RCAPHM15_0132', 'type': 'REGISTRY', 'domain': 'Assistance Publique Hôpitaux Marseille'}]}, 'armsInterventionsModule': {'armGroups': [{'type': 'EXPERIMENTAL', 'label': 'recently diagnosed ALS patients', 'interventionNames': ['Other: ALS Functional rating Scale-revised (ALS FRS-R)', 'Other: slow vital capacity', 'Other: Blood sample', 'Other: Cerebrospinal Fluid (CSF) sample']}, {'type': 'EXPERIMENTAL', 'label': 'not recently diagnosed ALS patients', 'interventionNames': ['Other: ALS Functional rating Scale-revised (ALS FRS-R)', 'Other: slow vital capacity', 'Other: Blood sample', 'Other: Cerebrospinal Fluid (CSF) sample']}, {'type': 'ACTIVE_COMPARATOR', 'label': 'patients with peripheral neuropathy, recently diagnosed', 'interventionNames': ['Other: Blood sample']}], 'interventions': [{'name': 'ALS Functional rating Scale-revised (ALS FRS-R)', 'type': 'OTHER', 'armGroupLabels': ['not recently diagnosed ALS patients', 'recently diagnosed ALS patients']}, {'name': 'slow vital capacity', 'type': 'OTHER', 'armGroupLabels': ['not recently diagnosed ALS patients', 'recently diagnosed ALS patients']}, {'name': 'Blood sample', 'type': 'OTHER', 'armGroupLabels': ['not recently diagnosed ALS patients', 'patients with peripheral neuropathy, recently diagnosed', 'recently diagnosed ALS patients']}, {'name': 'Cerebrospinal Fluid (CSF) sample', 'type': 'OTHER', 'armGroupLabels': ['not recently diagnosed ALS patients', 'recently diagnosed ALS patients']}]}, 'contactsLocationsModule': {'locations': [{'zip': '13005', 'city': 'Marseille', 'status': 'RECRUITING', 'country': 'France', 'contacts': [{'name': 'Joelle Micallef', 'role': 'CONTACT', 'email': 'joelle.micallef@ap-hm.fr'}], 'facility': 'Assistance Publique Hôpitaux de Marseille', 'geoPoint': {'lat': 43.29695, 'lon': 5.38107}}], 'centralContacts': [{'name': 'Joelle Micallef', 'role': 'CONTACT', 'email': 'joelle.micallef@ap-hm.fr'}], 'overallOfficials': [{'name': 'Urielle Desalbres', 'role': 'STUDY_DIRECTOR', 'affiliation': 'Assistance Publique Hôpitaux de Marseille'}]}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': 'Assistance Publique Hopitaux De Marseille', 'class': 'OTHER'}, 'responsibleParty': {'type': 'SPONSOR'}}}}