- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01601158
Umbilical Cord Blood Therapy for Children With Global Developmental Delay
Safety and Efficacy of Allogeneic Umbilical Cord Blood Therapy for Children With Global Developmental Delay
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Global developmental delay (GDD) is a subset of developmental disabilities defined as significant delay in two or more of the following developmental domains: gross/fine motor, speech/language, cognition, social/personal, and activities of daily living.
Umbilical cord blood has been used for inherited metabolic diseases that feature global developmental delay and many experimental animal studies have revealed umbilical cord blood is useful to repair neurological impairments in brain.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
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Gyeonggi-do
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Seongnam-si, Gyeonggi-do, Korea, Republic of, 463-712
- Cha Bundang Medical Center, Cha University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Global developmental delay
- Willing to comply with all study procedure
Exclusion Criteria:
- Medical instability including pneumonia or renal function at enrollment
- Poor cooperation of guardian,including inactive attitude for rehabilitation and visits for follow-up
- Uncontrolled persistent epilepsy
- Not eligible according to the principal investigator
Study Plan
How is the study designed?
Design Details
- Primary Purpose: TREATMENT
- Allocation: NA
- Interventional Model: SINGLE_GROUP
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
EXPERIMENTAL: Umbilical Cord Blood and Rehabilitation
Allogeneic Umbilical Cord Blood infusion and Active Rehabilitation
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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.
The subjects will be undertaken allogeneic umbilical cord blood infusion intravenously or intraarterially under non-myeloablative immunosuppression.
Other Names:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Changes in Cognition
Time Frame: Baseline - 6 months - 12 months
|
Korean Wechsler Preschool and Primay Scale of Intelligence (K-WPPSI) (Higher value means better cognitive function (K-WPPSI: below 70 - worst, over 130 - best).
The investigators will report K-WPPSI at each assessment time points.
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Baseline - 6 months - 12 months
|
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Changes in Cognitive Neurodevelopmental Outcome
Time Frame: Baseline - 1 month - 3 months - 6 months - 12 months
|
Korean version of Bayley Scale of Infant Development-II (K-BSID-II) Mental Scales (Higher value means better cognitive function, K-BSID-II mental scale raw score: 0 - worst, 178 - best).
The investigators will report K-BSID-II Mental Scale raw scores at each assessment time points.
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Baseline - 1 month - 3 months - 6 months - 12 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Changes in Motor Performance
Time Frame: Baseline - 1 month - 3 months - 6 months - 12 months
|
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).
The investigators will report GMPM scores at each assessment time points.
|
Baseline - 1 month - 3 months - 6 months - 12 months
|
|
Changes in Standardized Gross Motor Function
Time Frame: Baseline - 1 month - 3 months - 6 months - 12 months
|
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).
The investigators will report GMFM scores at each assessment time points.
|
Baseline - 1 month - 3 months - 6 months - 12 months
|
|
Changes in Motor Neurodevelopmental Outcome
Time Frame: Baseline - 1 month - 3 months - 6 months - 12 months
|
Korean version of Bayley Scale of Infant Development-II (K-BSID-II) Motor Scales (higher value means better motor function: 0 - worst, 111 - best).
The investigators will report K-BSID-II Motor Scale raw scores at each assessment time points.
|
Baseline - 1 month - 3 months - 6 months - 12 months
|
|
Changes in Functional Independence in Daily Activities
Time Frame: Baseline - 1 month - 3 months - 6 months - 12 months
|
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.
The investigators will report total WeeFIM scores measured at each assessment time points.
|
Baseline - 1 month - 3 months - 6 months - 12 months
|
|
Changes in Visual Perception Test
Time Frame: Baseline - 1 month - 3 months - 6 months - 12 months
|
We will evaluate visual perception function 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
|
Baseline - 1 month - 3 months - 6 months - 12 months
|
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Changes in Muscle Strength
Time Frame: Baseline - 1 month - 3 months - 6 months - 12 months
|
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.
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Baseline - 1 month - 3 months - 6 months - 12 months
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Changes in Functional Performance in Daily Activities
Time Frame: Baseline - 1 month - 3 months - 6 months - 12 months
|
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.
|
Baseline - 1 month - 3 months - 6 months - 12 months
|
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Changes in Language Evaluation
Time Frame: Baseline - 6 months - 12 months
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Sequenced Language Scale for Infant (SELSI), Preschool Receptive-Expressive Language Scale (PRES) or Korean Western Aphasia Battery (K-WAB) will be used depending on age and function.
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Baseline - 6 months - 12 months
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ESTIMATE)
Study Record Updates
Last Update Posted (ESTIMATE)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- GDDUCB
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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