Early hGH Treatment of SGA Infants to Prevent Irreversible Neurologic and Psychological Damage and Sequelae (hGH)
Primary Purpose
Infant, Small for Gestational Age, Growth Hormone Treatment, Infant, Premature, Diseases
Status
Unknown status
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
Human growth hormone,ZOMACTON® (somatropin)
Sponsored by
About this trial
This is an interventional treatment trial for Infant, Small for Gestational Age focused on measuring Small for gestational age (SGA), Human growth hormone (hGH)
Eligibility Criteria
Inclusion Criteria:
- Symmetrical small for gestational age at birth: weight + length+ head circumference below -2 SD for gestational age.
- Birth weight of 1200-2200 gr
- Follow-up of growth until age of 6-12 months
- Growth parameters below -2 SD at age of 6-12 months and absence of sufficient catch-up.
- Low growth hormone levels.
Exclusion Criteria:
- Chromosomal aberration
- Any congenital syndrome and any syndrome that shows a tendency to uncontrolled cell growth and to develop tumors
- Major congenital malformation (affecting growth or development)
- Congenital infection
- Exposure to teratogenic drugs or drugs affecting development during pregnancy
- Maternal drug or alcohol abuse.
- Maternal cancer as well as cancer in 1st degree relatives.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
No Intervention
Arm Label
hGH, ZOMACTON® (somatropin)
No human growth hormone
Arm Description
For infants in the treatment group receiving ZOMACTON® (somatropin) growth hormone by injection
No growth hormone is given.
Outcomes
Primary Outcome Measures
Changes in Cognitive assessments (using the Bayley Scales of Infant Development (BSID-III)
using the Bayley Scales of Infant Development (BSID-III)
Changes in Neurological status (formal neurological examination)
using formal neurological examination
Secondary Outcome Measures
Changes in X-ray of the hand and wrist
Pediatric Quality of life Inventory: the PedsQL measure
Achenbach Child Behavior Checklist (CBCL)
Full Information
NCT ID
NCT02326610
First Posted
November 26, 2014
Last Updated
December 26, 2014
Sponsor
Tel-Aviv Sourasky Medical Center
1. Study Identification
Unique Protocol Identification Number
NCT02326610
Brief Title
Early hGH Treatment of SGA Infants to Prevent Irreversible Neurologic and Psychological Damage and Sequelae
Acronym
hGH
Official Title
Early hGH Treatment of Symmetrically Born Small for Gestational Age Infants to Prevent Irreversible Neurologic and Psychological Damage and Sequelae
Study Type
Interventional
2. Study Status
Record Verification Date
December 2014
Overall Recruitment Status
Unknown status
Study Start Date
December 2014 (undefined)
Primary Completion Date
December 2017 (Anticipated)
Study Completion Date
December 2018 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Tel-Aviv Sourasky Medical Center
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
SGA Infants who do not show a developmental catch-up growth within the first 6 months of life fall in the category of SGA children shown to have defects in the GH/IGF-I axis, resulting in partial hGH/IGF-I deficiency.
Up to 1/4 of children born SGA have neurodevelopmental deficits. The partial hGH/IGF-I deficiency in SGA children can be the major or contributory cause of to their neurodevelopmental deficits
To assess the effect of early growth hormone treatment given to symmetrical small for gestational age (SGA) infants not demonstrating catch-up growth on neurodevelopment and growth between birth and 6-12 months.
The study is an innovative research not previously performed for improving neurodevelopmental outcome of SGA infants. As this is the first study of its kind, the safety of use of GH has not been reported, however based on multiple studies assessing use of GH in infants and young children, it is reasonable to similarly expect no short and long-term adverse effects.
The study will take place at the Tel Aviv Medical Center only.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Infant, Small for Gestational Age, Growth Hormone Treatment, Infant, Premature, Diseases
Keywords
Small for gestational age (SGA), Human growth hormone (hGH)
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
20 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
hGH, ZOMACTON® (somatropin)
Arm Type
Active Comparator
Arm Description
For infants in the treatment group receiving ZOMACTON® (somatropin) growth hormone by injection
Arm Title
No human growth hormone
Arm Type
No Intervention
Arm Description
No growth hormone is given.
Intervention Type
Drug
Intervention Name(s)
Human growth hormone,ZOMACTON® (somatropin)
Intervention Description
The initial dose will be 30µg/kg/day. The maximal dose will be 40µg/kg/day. The dose will be adjusted by monitoring the serum IGF-I level. Growth hormone will be delivered by injection.
Primary Outcome Measure Information:
Title
Changes in Cognitive assessments (using the Bayley Scales of Infant Development (BSID-III)
Description
using the Bayley Scales of Infant Development (BSID-III)
Time Frame
Before treatment and 1 year later
Title
Changes in Neurological status (formal neurological examination)
Description
using formal neurological examination
Time Frame
Before treatment and 1 year later
Secondary Outcome Measure Information:
Title
Changes in X-ray of the hand and wrist
Time Frame
Before treatment and 1 year later
Title
Pediatric Quality of life Inventory: the PedsQL measure
Time Frame
after 1 year of treatment
Title
Achenbach Child Behavior Checklist (CBCL)
Time Frame
at the end of study after 1 year of treatment
10. Eligibility
Sex
All
Minimum Age & Unit of Time
6 Months
Maximum Age & Unit of Time
12 Months
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Symmetrical small for gestational age at birth: weight + length+ head circumference below -2 SD for gestational age.
Birth weight of 1200-2200 gr
Follow-up of growth until age of 6-12 months
Growth parameters below -2 SD at age of 6-12 months and absence of sufficient catch-up.
Low growth hormone levels.
Exclusion Criteria:
Chromosomal aberration
Any congenital syndrome and any syndrome that shows a tendency to uncontrolled cell growth and to develop tumors
Major congenital malformation (affecting growth or development)
Congenital infection
Exposure to teratogenic drugs or drugs affecting development during pregnancy
Maternal drug or alcohol abuse.
Maternal cancer as well as cancer in 1st degree relatives.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Dror Mandel, MD
Phone
+97236925690
Email
drorm@tlvmc.gov.il
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dror Mandel, MD
Organizational Affiliation
Department of Neonatology, Tel Aviv Medical Center, 64239 Tel Aviv, Israel
Official's Role
Principal Investigator
12. IPD Sharing Statement
Learn more about this trial
Early hGH Treatment of SGA Infants to Prevent Irreversible Neurologic and Psychological Damage and Sequelae
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