Ignite Creation Date:
2025-12-25 @ 4:32 AM
Ignite Modification Date:
2026-02-24 @ 11:50 AM
Study NCT ID:
NCT05631418
Status:
WITHDRAWN
Last Update Posted:
2023-02-23
First Post:
2022-10-23
Is Gene Therapy:
True
Has Adverse Events:
False
Brief Title:
Chinese Regional Spinal Muscular Atrophy Patient Registration Study
Sponsor:
Organization:
Raw JSON
{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}, 'conditionBrowseModule': {'meshes': [{'id': 'D009134', 'term': 'Muscular Atrophy, Spinal'}], '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': 'D009468', 'term': 'Neuromuscular Diseases'}]}}, 'protocolSection': {'designModule': {'bioSpec': {'retention': 'SAMPLES_WITH_DNA', 'description': 'Genomic DNA may be extracted from the whole blood samples of the patients to carry out the genetic testing.'}, 'studyType': 'OBSERVATIONAL', 'designInfo': {'timePerspective': 'OTHER', 'observationalModel': 'COHORT'}, 'enrollmentInfo': {'type': 'ACTUAL', 'count': 0}, 'targetDuration': '3 Years', 'patientRegistry': True}, 'statusModule': {'whyStopped': 'Due to the lack of application materials, the normal research can not be carried out for the time being.', 'overallStatus': 'WITHDRAWN', 'startDateStruct': {'date': '2022-11', 'type': 'ESTIMATED'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2023-02', 'completionDateStruct': {'date': '2026-12', 'type': 'ESTIMATED'}, 'lastUpdateSubmitDate': '2023-02-22', 'studyFirstSubmitDate': '2022-10-23', 'studyFirstSubmitQcDate': '2022-11-20', 'lastUpdatePostDateStruct': {'date': '2023-02-23', 'type': 'ACTUAL'}, 'studyFirstPostDateStruct': {'date': '2022-11-30', 'type': 'ACTUAL'}, 'primaryCompletionDateStruct': {'date': '2025-12', 'type': 'ESTIMATED'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'World Health Organization (WHO) motor milestone change', 'timeFrame': 'baseline, 0.5 year, 1 year, 1.5 year, 2 year, 2.5 year, 3 year', 'description': "Treated and untreated patients with SMA Type 1-3: change of WHO motor milestone from baseline to 3 years to track the patients' motor functional development/status. World Health Organization motor milestone score ranges from 0 to 18. The higher the score is, the better the motor function is."}, {'measure': 'Hammersmith Infant Neurological Examination-2 (HINE-2) scale score change', 'timeFrame': 'baseline, 0.5 year, 1 year, 1.5 year, 2 year, 2.5 year, 3 year', 'description': "Treated and untreated patients with SMA Type 1-3: change of HINE-2 scale score from baseline to 3 years to help track the patients' motor functional development/status. The HINE-2 scale score ranges from 0 to 26. The higher the score is, the better the motor function is."}, {'measure': "Self-reporting/Caregivers' reporting collection", 'timeFrame': 'baseline, 0.5 year, 1 year, 1.5 year, 2 year, 2.5 year, 3 year', 'description': 'Treated and untreated patients with SMA Type 1-3: motor function change acquired from patients themselves and their caregivers. (Subjective reports were collected through interviews and no evaluation scale was used here.)'}, {'measure': "Motor function evalution-Children's Hospital of Philadelphia Infant Test of Neuromuscular Disorders(CHOP INTEND) scale", 'timeFrame': 'treated/untreated: baseline, 0.5 year, 1 year, 1.5 year, 2 year, 2.5 year, 3 year', 'description': 'For children ≤ 2 years: change of CHOP INTEND scale score. The CHOP INTEND scale score ranges from 0 to 64. The higher the score is, the better the motor function is.'}, {'measure': 'Motor function evalution-Hammersmith Functional Motor Scale-Expanded(HFMSE) scale', 'timeFrame': 'treated/untreated: baseline, 0.5 year, 1 year, 1.5 year, 2 year, 2.5 year, 3 year', 'description': 'For children older than 2 years, ambulatory or not: Change of HFMSE scale score. The scale score ranges from 0 to 66. The higher the score is, the better the motor function is.'}, {'measure': 'Motor function evalution-Revised Upper Limb Module(RULM) scale', 'timeFrame': 'treated/untreated: baseline, 0.5 year, 1 year, 1.5 year, 2 year, 2.5 year, 3 year', 'description': 'For children children older than 6 years, ambulatory or not: Change of RULM (Revised Upper Limb Module) scale score. The scale score ranges from 0 to 37. The higher the score is, the better the motor function is.'}, {'measure': 'Motor function evalution change-6 minutes walking test(6MWT)', 'timeFrame': 'treated/untreated: baseline, 0.5 year, 1 year, 1.5 year, 2 year, 2.5 year, 3 year', 'description': "For ambulatory individuals: added the change of 6MWT from baseline to 3 years to test exercise endurance. (The walking distance within 6 minutes is taken as the evaluation index, and there's no specific score range.)"}, {'measure': 'Yearly changes of incidence and morbi-mortality-vital events', 'timeFrame': 'every year for 3 years', 'description': 'Events of newly diagnosis, hospitalizations, recurrent infections, fractures, complications and death.'}, {'measure': 'Change from baseline respiratory function', 'timeFrame': 'baseline(before treatment), 1 year, 2 year, 3 year', 'description': 'Onset of respiratory support or change in the mode and time (including intubations).'}, {'measure': 'Change from baseline digestive-nutritional function', 'timeFrame': 'baseline(before treatment), 0.5 year, 1 year, 1.5 year, 2 year, 2.5 year, 3 year', 'description': 'Digestive events, onset of nutritional support or change in the mode and time and special intervention.'}, {'measure': 'Change from baseline spinal scoliosis Cobb angle', 'timeFrame': 'baseline(before treatment), 1 year, 2 year, 3 year', 'description': 'Onset of spinal deformity, or increment of over 5° in the Cobb angle (examination in supine position or in the upright position, with or without brace, with or without implant (surgery), and the change of the bone mineral density in lumbar.'}], 'secondaryOutcomes': [{'measure': 'Pulmonary function', 'timeFrame': 'baseline(before treatment), 1 year, 2 year, 3 year', 'description': 'Pulmonary Function Test （PFT）will be evaluated at least once per year for children \\> 5 years, by specifying the posture of realization of the test, lying vs sitting.'}, {'measure': 'Cardiological function monitoring', 'timeFrame': 'baseline(before treatment), 1 year, 2 year, 3 year', 'description': "Conventional echocardiography will be evaluated to monitor the patients' cardiac function."}, {'measure': 'Body composition measurement-Lean body mass', 'timeFrame': 'baseline(before treatment), 1 year, 2 year, 3 year', 'description': 'Lean body mass will be measured in patients older than three years by DXA or Inbody device at least once a year.'}, {'measure': 'Body composition measurement-Fat mass', 'timeFrame': 'baseline(before treatment), 1 year, 2 year, 3 year', 'description': 'Fat mass will be measured in patients older than three years by DXA or Inbody device at least once a year.'}, {'measure': 'Biomarkers', 'timeFrame': 'baseline(before treatment), 0.5 year, 1 year, 1.5 year, 2 year, 2.5 year, 3 year', 'description': 'Change of biomarkers: such as Neurofilaments.'}, {'measure': "Patients and caregivers' quality of life", 'timeFrame': 'baseline(before treatment), 1 year, 2 year, 3 year', 'description': 'Questionary as the "PedsQL Child report/PedsQL parent report concerning child" will be used to evaluate patient\'s quality of life. The Pediatric Quality of Life Inventory Measurement Models (PedsQLTM) is used for this evalution. The minimum score is 0 and no specific maximum score of this scale. The higher the score is, the higher the quality of life is.'}]}, 'oversightModule': {'oversightHasDmc': False, 'isFdaRegulatedDrug': False, 'isFdaRegulatedDevice': False}, 'conditionsModule': {'keywords': ['Spinal Muscular Atrophy', 'long-term follow-up', 'quality of life', 'disease-modifying treatment', 'clinical efficacy', 'disease prognosis', 'newborn screening'], 'conditions': ['Recruitment']}, 'descriptionModule': {'briefSummary': "The primary objectives of this study are to obtain clinically meaningful data on the survival, outcomes, prognosis and treatment effect of all the patients with spinal muscular atrophy (SMA) 5q types 1 to 3 (according to international classification), being followed in the Children's Hospital, Zhejiang University School of Medicine since October 2019. The registry will collect retrospectively and prospectively the longitudinal data of the long-term follow-up for children patients, under real life conditions of current medical practice, in order to document the clinical evolution of patients (survival, motor, respiratory, orthopedic and nutritional and so on), the conditions of use of the treatments, the mortality rates of treated and untreated patients, the tolerance of the treatments, adverse events.", 'detailedDescription': "The detailed objectives of this study included but not be limited to the following aspects:\n\n1. to collect and describe overall demographic, familial, clinical, biological, and genetic characteristics of patients with 5qSMA diagnosed and treated in regions of China, by the type of SMA (type 1,2, and 3);\n2. to study the impact of proactive and symptomatic medical interventions (such as bracing) and medications (disease-modifying treatment, anti-infectious, digestive, nutritional supplements, ect.) in the evolution of patients;\n3. to study the long-term evolution (survival, motor and respiratory functions, spinal shape, growth and nutritional function) of 5qSMA in treated and untreated populations, by new available therapies;\n4. to study the incidence and mortality rate of 5qSMA in treated and untreated populations;\n5. to identify and document the different therapeutic strategies by sub-populations and by discontinuation or follow-up of treatments;\n6. to evaluate prognostic factors of responses to different drug therapies;\n7. to study the tolerance of treatments by type of treatments, by type of SMA and overall tolerance (including adverse events);\n8. to help popularize newborn screening for SMA and pre-symptom treatment among Chinese population;\n9. to get knowledge of the probable costs of care for 5qSMA patients in different groups (disease types, ages);\n10. to provide needful elements to evaluate the health care costs for the disease;\n11. to study the autonomy and the quality of life of patients depending on different therapies and the impact on patients' caregivers;\n12. to help facilitate development of basic research on SMA in the conduct of trials on new treatment."}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['CHILD', 'ADULT'], 'maximumAge': '18 Years', 'samplingMethod': 'PROBABILITY_SAMPLE', 'studyPopulation': 'Genetically confirmed 5qSMA patients through 1 to 3 types younger than 18 years old followed in our hospital since October 2019 with or without disease-modifying treatment.', 'healthyVolunteers': False, 'eligibilityCriteria': 'Inclusion Criteria:\n\n1. Genetically confirmed 5qSMA patients through 1 to 3 types younger than 18 years old followed in our hospital since October 2019;\n2. For prospective study: inform consent form signed by patient;\n3. Not combined with any other genetic and metabolic diseases;\n\nExclusion Criteria:\n\n1. Other type of SMA (not 5q).\n2. Under guardianship or curatorship.\n3. Unable to understand or cooperate with the study.'}, 'identificationModule': {'nctId': 'NCT05631418', 'briefTitle': 'Chinese Regional Spinal Muscular Atrophy Patient Registration Study', 'organization': {'class': 'OTHER', 'fullName': "The Children's Hospital of Zhejiang University School of Medicine"}, 'officialTitle': "The Children's Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child Health", 'orgStudyIdInfo': {'id': 'CHZhejiang'}}, 'contactsLocationsModule': {'locations': [{'zip': '310052', 'city': 'Hangzhou', 'country': 'China', 'facility': "The Children's Hospital, Zhejiang University School of Medicine", 'geoPoint': {'lat': 30.29365, 'lon': 120.16142}}], 'overallOfficials': [{'name': 'Shanshan Mao, MD', 'role': 'PRINCIPAL_INVESTIGATOR', 'affiliation': "The Children's Hospital of Zhejiang University School of Medicine"}]}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': "The Children's Hospital of Zhejiang University School of Medicine", 'class': 'OTHER'}, 'responsibleParty': {'type': 'PRINCIPAL_INVESTIGATOR', 'investigatorTitle': 'Director', 'investigatorFullName': 'Shanshan Mao', 'investigatorAffiliation': "The Children's Hospital of Zhejiang University School of Medicine"}}}}