Ignite Creation Date:
2025-12-24 @ 9:19 PM
Ignite Modification Date:
2025-12-29 @ 11:01 PM
Study NCT ID:
NCT01639404
Status:
COMPLETED
Last Update Posted:
2013-08-12
First Post:
2012-07-10
Is NOT Gene Therapy:
True
Has Adverse Events:
False
Brief Title:
Umbilical Cord Blood Therapy for Children With Cerebral Palsy
Sponsor:
Organization:
Raw JSON
{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}, 'conditionBrowseModule': {'meshes': [{'id': 'D002547', 'term': 'Cerebral Palsy'}], 'ancestors': [{'id': 'D001925', 'term': 'Brain Damage, Chronic'}, {'id': 'D001927', 'term': 'Brain Diseases'}, {'id': 'D002493', 'term': 'Central Nervous System Diseases'}, {'id': 'D009422', 'term': 'Nervous System Diseases'}]}}, 'protocolSection': {'designModule': {'phases': ['NA'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'allocation': 'NA', 'maskingInfo': {'masking': 'NONE'}, 'primaryPurpose': 'TREATMENT', 'interventionModel': 'SINGLE_GROUP'}, 'enrollmentInfo': {'type': 'ACTUAL', 'count': 17}}, 'statusModule': {'overallStatus': 'COMPLETED', 'startDateStruct': {'date': '2012-07'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2013-08', 'completionDateStruct': {'date': '2013-03', 'type': 'ACTUAL'}, 'lastUpdateSubmitDate': '2013-08-08', 'studyFirstSubmitDate': '2012-07-10', 'studyFirstSubmitQcDate': '2012-07-10', 'lastUpdatePostDateStruct': {'date': '2013-08-12', 'type': 'ESTIMATED'}, 'studyFirstPostDateStruct': {'date': '2012-07-12', 'type': 'ESTIMATED'}, 'primaryCompletionDateStruct': {'date': '2013-03', 'type': 'ACTUAL'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'Changes in Motor Performance', 'timeFrame': 'Baseline - 1 month - 3 months', 'description': 'GMPM (Gross Motor Performance Measure) as a standardized measurement tool for assessing quality of movement regarding 3 properties of 5 ones; alignment, coordination, dissociated movement, stability, and weight shift (range: 0\\~100, Higher value means better motor quality). GMPM scores at each assessment time points will be reported.'}, {'measure': 'Changes in Standardized Gross Motor Function', 'timeFrame': 'Baseline - 1 month - 3 months', 'description': 'GMFM (Gross Motor Function Measure) as a standardized measurement tool for assessing Gross Motor Function consisting of sub-scales; lying \\& rolling, sitting, crawling \\& kneeling, standing, walking, running \\& jumping (range: 0\\~100 , Higher value means better gross motor function). GMFM scores at each assessment time points will be reported.'}], 'secondaryOutcomes': [{'measure': 'Changes in Cognitive Neurodevelopmental Outcome', 'timeFrame': 'Baseline - 1 month - 3 months', 'description': 'Korean version of Bayley Scale of Infant Development-II (K-BSID-II) Mental Scales (higher value means better mental function: 0 - worst, 178 - best). K-BSID-II Mental Scale raw scores at each assessment time points will be reported.'}, {'measure': 'Changes in Motor Neurodevelopmental Outcome', 'timeFrame': 'Baseline - 1 month - 3 months', 'description': 'Korean version of Bayley Scale of Infant Development-II (K-BSID-II) Motor Scales (higher value means better motor function: 0 - worst, 112 - best). K-BSID-II Motor Scale raw scores at each assessment time points will be reported.'}, {'measure': 'Changes in Functional Independence in Daily Activities', 'timeFrame': 'Baseline - 1 month - 3 months', 'description': 'WeeFIM (Functional Independence Measure for Children) measures functional independence in daily activities. WeeFIM contains 18 items and each item is ranked from complete dependence (scored as 1) to complete independence (scored as 7). The range is from 18 to 126 and higher scores mean more independent performance in daily activities. Total WeeFIM scores measured at each assessment time points will be reported.'}, {'measure': 'Changes in Visual Perception Test', 'timeFrame': 'Baseline - 1 month - 3 months', 'description': 'Visual perception function will be evaluated with one of three measures: DTVP (Developmental Test of Visual Perception), MVPT (Motor-free Visual Perception Test), and VMI (Visual-Motor Integration, Visual Perception and Motor Coordination). All can be scored as percentile rank from 0 to 100. Higher values mean better visual perception ability.'}, {'measure': 'Changes in Muscle Strength', 'timeFrame': 'Baseline - 1 month - 3 months', 'description': 'Summation of MMT (manual muscle strength test score): summated scores of the manual muscle strength test (zero=0, trace=1, poor=2, fair=3, good=4, normal=5) for flexors, extensors, abductors, and adductors of bilateral shoulder and hip joints; flexors and extensors of bilateral elbow, wrist, and knee; dorsiflexors and plantar flexors of the ankles (range: 0 \\~ 160) Higher scores mean better muscle strength. Categories of outcome table will be summation of MMT scores measured at each assessment time point.'}, {'measure': 'Changes in Functional Performance in Daily Activities', 'timeFrame': 'Baseline - 1 month - 3 months', 'description': 'Pediatric Evaluation of Disability Inventory (PEDI) for assessing functional performance in daily activities in children (All values are adjusted and higher value means better functional performance, 0 - worst, 100 - best). We will report 2 scales and 3 domains of each scale: a Functional Skill Scale (FSS) and a Caregiver Assistance Scale (CAS) which are divided respectively into 3 domains: self care, mobility, and social function. Categories of outcome table will be each domain scores measured at each assessment time point.'}]}, 'oversightModule': {'oversightHasDmc': False}, 'conditionsModule': {'keywords': ['Cerebral Palsy', 'Umbilical Cord Blood', 'Rehabilitation'], 'conditions': ['Cerebral Palsy']}, 'descriptionModule': {'briefSummary': 'This study aims to evaluate the efficacy of umbilical cord blood therapy for children with cerebral palsy.', 'detailedDescription': 'Cerebral palsy is a disorder of movement and posture resulted from a non-progressive lesion or injury of the immature brain. It is a leading cause of childhood onset disability.\n\nMany experimental animal studies have revealed that umbilical cord blood is useful to repair neurological injury in brain.\n\nOn the basis of many experimental studies, umbilical cord blood is suggested as a potential therapy for cerebral palsy.'}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['CHILD', 'ADULT'], 'maximumAge': '20 Years', 'minimumAge': '6 Months', 'healthyVolunteers': False, 'eligibilityCriteria': 'Inclusion Criteria:\n\n* Cerebral Palsy with abnormal muscle tone\n* Gross Motor Function Classification System (GMFCS): I, II, III, IV, V\n* Willing to comply with all study procedure\n\nExclusion Criteria:\n\n* Medical illnesses including pneumonia or renal function at enrollment\n* Presence of known genetic disease\n* Presence of drug hypersensitivity which is related to this study remedy\n* Poor cooperation of guardian,including inactive attitude for rehabilitation and visits for follow-up\n* Decision by the principal investigator when there are unexpected events that may affect the outcomes'}, 'identificationModule': {'nctId': 'NCT01639404', 'briefTitle': 'Umbilical Cord Blood Therapy for Children With Cerebral Palsy', 'organization': {'class': 'OTHER', 'fullName': 'Bundang CHA Hospital'}, 'officialTitle': 'Allogeneic Umbilical Cord Blood Therapy for Children With Cerebral Palsy', 'orgStudyIdInfo': {'id': 'CPUCB'}}, 'armsInterventionsModule': {'armGroups': [{'type': 'EXPERIMENTAL', 'label': 'Umbilical Cord Blood and Rehabilitation', 'description': 'Allogeneic Umbilical Cord Blood Administration and Active Rehabilitation', 'interventionNames': ['Procedure: Umbilical Cord Blood Administration', 'Other: Active Rehabilitation']}], 'interventions': [{'name': 'Umbilical Cord Blood Administration', 'type': 'PROCEDURE', 'otherNames': ['Donated Umbilical Cord Blood Units from Affiliated Cord Blood Bank'], 'description': 'The subjects will be undertaken allogeneic umbilical cord blood infusion intravenously or intraarterially under non-myeloablative immunosuppression.', 'armGroupLabels': ['Umbilical Cord Blood and Rehabilitation']}, {'name': 'Active Rehabilitation', 'type': 'OTHER', 'description': 'All subjects should participate in active rehabilitation. They will receive two physical and occupational therapy sessions per day. Post discharge, each participant should continue to receive rehabilitation therapy at least 3 days per week until the study completion.', 'armGroupLabels': ['Umbilical Cord Blood and Rehabilitation']}]}, 'contactsLocationsModule': {'locations': [{'zip': '463-712', 'city': 'Seongnam-si', 'state': 'Gyeonggi-do', 'country': 'South Korea', 'facility': 'CHA Bundang Medical Center, CHA University', 'geoPoint': {'lat': 37.43861, 'lon': 127.13778}}], 'overallOfficials': [{'name': 'MinYoung Kim, M.D., Ph.D.', 'role': 'PRINCIPAL_INVESTIGATOR', 'affiliation': 'CHA University'}]}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': 'MinYoung Kim, M.D.', 'class': 'OTHER'}, 'responsibleParty': {'type': 'SPONSOR_INVESTIGATOR', 'investigatorTitle': 'Associate Professor', 'investigatorFullName': 'MinYoung Kim, M.D.', 'investigatorAffiliation': 'Bundang CHA Hospital'}}}}