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Found 39 clinical trials
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Primordial Dwarfism Registry

The goal of this registry is to collect information on individuals with Microcephalic Osteodysplastic Primordial Dwarfism Type II (also called MOPDII) and other forms of microcephalic primordial

  • 0 views
  • 26 Jan, 2021
  • 1 location
None
Web-based Adherence Information Integrated Nurse-led Monitoring Clinic

Non-adherence is a recognized problem with growth hormone treatment in children. In this study, we aim to utilize web-based information derived from easypod growth hormone injection devices and easypod connect devices in a nurse-led telephone clinic to improve adherence and therefore optimize growth. Our primary aim is to test height …

hormone deficiency
somatotropin
turner syndrome
growth hormone
growth hormone treatment
  • 11 views
  • 08 Oct, 2021
  • 1 location
None
Hypo-mineralization of Primary and Permanent Teeth in a Group of Children With Stunted Growth.A Cross Sectional Study.

The second primary molar (SPM) development start at the same time as development of the first permanent molars (FPM) and permanent incisors so any systemic disturbance - causing stunted growth -occur , will result in hypo-mineralization of SPM as well as FPM and permanent incisors (Butler 1967, Weerheijm and Mejre …

  • 0 views
  • 10 Mar, 2021
  • 1 location
None
Genetic Causes of Growth Disorders

Background Some growth disorders are caused by a change in genes. Genes are the instructions the body uses to function. Changes in genes often cause them not to work correctly. Researchers want to use a new technology called exome sequencing, to look at many genes at once. This is done …

hormone deficiency
somatotropin
Accepts healthy volunteers
growth hormone treatment
growth hormone
  • 70 views
  • 10 Oct, 2021
  • 3 locations
None
Natural History of the Collagen-Related Disorder Osteogenesis Imperfecta and Genotype Phenotype Correlation

, short stature, and bowing of the long bones. There is no known cure for OI so researchers want to learn more about it. Objectives To obtain a natural history of the

autosomal dominant
probe
hearing test
col1a2
col1a1
  • 10 views
  • 10 Oct, 2021
  • 1 location
None
Skeletal Muscle Effects of GH in Boys

deficiency or idiopathic short stature. Patients will be similarly short. The investigators will also compare these values in the short stature cohort to those obtained in testing performed in normally

hormone deficiency
somatotropin
GH deficiency
short stature
somatropin
  • 0 views
  • 26 Jan, 2021
  • 1 location
None
AVAST Anomalies Vasculaires Associ es au Syndrome de Turner (Vascular Abnormalities Associated With Turner Syndrome)

Turner syndrome is a genetic condition, rare, due to the total or partial absence of one X chromosome, affecting 1/2500 newborn female. It combines almost constantly short stature and ovarian

heart disease
arteriopathy
stenosis
vascular complications
short stature
  • 164 views
  • 24 Jan, 2021
  • 11 locations
None
Iodine Status in Pregnant Women and Their Newborns: is Congenital Hypothyroidism Related to Iodine Deficiency in Pregnancy?

Iodine is an essential component of thyroid hormone, which is necessary for many metabolic processes as well as the maturation of the CNS. Deficiencies of iodine have deleterious effects on both pregnant women and infants. The iodine status of the population after implementation of the universal salt iodization program in …

thyroid function test
  • 3 views
  • 07 Nov, 2020
  • 1 location
None
An Observational/Natural History Study of Cockayne Syndrome

This is an Observational Study of pediatric patients diagnosed with Cockayne Syndrome (CS) to assess the natural progression of that disease, with special attention to hearing and physical changes in length or height, weight, head circumference, and arm span during "standard-of-care" treatment. A portion of this information will be collected …

  • 20 views
  • 08 Nov, 2020