Umbilical Cord Blood Therapy for Global Developmental Delay

Sponsor
MinYoung Kim, M.D. (Other)
Overall Status
Completed
CT.gov ID
NCT01769716
Collaborator
CHA University (Other)
14
1
1
60
0.2

Study Details

Study Description

Brief Summary

This open-label study aims to evaluate the safety and efficacy of autologous or allogeneic umbilical cord blood therapy for children with global developmental delay.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Umbilical cord blood transplantation
N/A

Detailed Description

Global developmental delay is 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 Design

Study Type:
Interventional
Actual Enrollment :
14 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Intervention Model Description:
allogeneic cord blood transplantation for children with developmental delayallogeneic cord blood transplantation for children with developmental delay
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Umbilical Cord Blood Therapy for Children With Global Developmental Delay
Study Start Date :
Dec 1, 2012
Actual Primary Completion Date :
Dec 1, 2017
Actual Study Completion Date :
Dec 1, 2017

Arms and Interventions

Arm Intervention/Treatment
Experimental: Umbilical cord blood transplantation

Allogeneic umbilical cord blood will be administered intravenously or intraarterially under non-myeloablative immunosuppression. In case of autologous umbilical cord blood, immunosuppression is not required.

Procedure: Umbilical cord blood transplantation
Other Names:
  • Autologous or Allogeneic Umbilical Cord Blood
  • Outcome Measures

    Primary Outcome Measures

    1. Changes in Cognition [Baseline - 6 months - 12 months]

      Korean Wechsler Preschool and Primary Scale of Intelligence (K-WPPSI) (Higher value means better cognitive function (K-WPPSI: below 70 - worst, over 130 - best)

    2. Changes in Cognitive Neurodevelopmental Outcome [Baseline - 1 month - 3 months - 6 months - 12 months]

      Korean version of Bayley Scale of Infant Development-II Mental Scales (Higher value means better cognitive function: raw score 0 - worst, 178 - best.)

    Secondary Outcome Measures

    1. Changes in Motor Performance [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.)

    2. Changes in Standardized Gross Motor Function [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.)

    3. Changes in Motor Neurodevelopmental Outcome [Baseline - 1 month - 3 months - 6 months - 12 months]

      Korean version of Bayley Scale of Infant Development-II Motor Scales (Higher value means better motor function: raw score 0 - worst, 112 - best)

    4. Changes in Functional Independence in Daily Activities [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.

    5. Changes in Visual Perception Test [Baseline - 1 month - 3 months - 6 months - 12 months]

      Visual perception function is evaluated with one of three measures: DTVP (Developmental Test of Visual Perception), MVPT (Motor-free Visual Perception Test), and VMI (Visual-Motor Integration). All can be scored as percentile rank from 0 to 100. Higher values mean better visual perception ability.

    6. Changes in Muscle Strength [Baseline - 1 month - 3 months - 6 months - 12 months]

      Summation of MMT (manual muscle testing): 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.

    7. Changes in Functional Performance in Daily Activities [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.)

    8. Changes in Language Evaluation [Baseline - 6 months - 12 months]

      Sequenced Language Scale for Infant (SELSI), Preschool Receptive-Expressive Language Scale (PRES) or Korean Western Aphasia Battery (K-WAB)

    9. Changes in Brain glucose metabolism [Baseline - 12 months]

      FDG-PET

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    6 Months to 15 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    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

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 CHA Bundang Medical Center, CHA University Seongnam-si Gyeonggi-do Korea, Republic of 463-712

    Sponsors and Collaborators

    • MinYoung Kim, M.D.
    • CHA University

    Investigators

    • Principal Investigator: MinYoung Kim, M.D., Ph.D., CHA University

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    MinYoung Kim, M.D., Associate Professor, Bundang CHA Hospital
    ClinicalTrials.gov Identifier:
    NCT01769716
    Other Study ID Numbers:
    • UCBGDD
    First Posted:
    Jan 17, 2013
    Last Update Posted:
    Jan 23, 2018
    Last Verified:
    Jan 1, 2018
    Keywords provided by MinYoung Kim, M.D., Associate Professor, Bundang CHA Hospital

    Study Results

    No Results Posted as of Jan 23, 2018