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NCT Number: NCT00562705

Effects of Growth Hormone (GH) Treatment on Eating Regulation

This is a two arm, randomized, prospective, intervention study in order to determine the effects of growth hormone treatment on eating regulation and to compare between the growth responses with or without nutritional intervention in short stature children.

The study will include 30 short stature children that are about to initiate growth hormone treatment and will last for one year. After 4 months of treatment, children will be randomized into two groups:

1. Control group that will continue with growth hormone treatment without any other intervention. 2. Study group that will be a given a nutritional intervention in addition to growth hormone treatment.

At screening visit and during the study the following parameters will be evaluated: height, weight, growth markers in the blood and urine, child eating behavior questionnaire, blood tests, hormonal tests and resting energy expenditure measurements.

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Key information

Age range

2 year–18 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Schneider Children's Medical Center

Petah Tikva, Israel

About this study

This is a two arm, randomized, prospective, intervention study in order to determine the effects of growth hormone treatment on eating regulation and to compare between the growth responses with or without nutritional intervention in short stature children.

Background:

In the last three decades children with different kinds of short stature pathologies were treated with growth hormone. Most of the attention in growth hormone studies is focused on the effect of the treatment on growth. Today there are very few studies that are focused on the effect of growth hormone on eating regulations and the connection between eating regulations and growth improvement in growth hormone treatment.

Objectives:

  • To evaluate the effect of short term growth hormone treatment on the following parameters:
  • Appetite, food preference, amount of food and ingredients.
  • Changes in food regulations.
  • Changes in body composition.
  • Changes in resting energy expenditure.
  • Changes in hormones that are associated with appetite and with energy balance: IGF-1,IGFBP1&3 and Ghrelin.
  • Changes in metabolic and nutritional measurements: glucose, insulin, lipid profile, total proteins, albumin, liver functions, alkaline-phosphatase, hemoglobin, transferrin, iron, B12, folic acid.
  • To evaluate the effect of nutritional support on growth rate in one year growth hormone treatment.
  • To evaluate changes in growth markers in the serum and urine during growth hormone treatment.

Methods:

The study will include 30 short stature children that are about to initiate growth hormone treatment and will last for one year. After 4 months of treatment children will be randomized into two groups:

  • Control group that will continue with growth hormone treatment without any other intervention.
  • Study group that will be given a nutritional intervention In addition to growth hormone treatment.

The nutritional intervention will include nutritional consultation and applying a personal dietetic menu. At screening visit and during the study the following parameters will be evaluated: height, weight, growth markers in the blood and urine, food diary, child eating behavior questionnaire, resting energy expenditure measurements, blood tests, hormonal tests and fasting and post-prandial levels of leptin, ghrelin, GLP-1, insulin and glucose.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Height of at least 2.0 standard deviations below the mean height for chronological age and sex according to the 2000 standards from the Centers for Disease Control and Prevention (CDC).
  • Children that have one of the following short stature pathologies:
  • IGHD or MPHD
  • ISS
  • SGA
  • Proper function of thyroid gland, kidney and liver
  • Prior to initiating growth hormone treatment

Exclusion criteria

  • Chronic diseases
  • Diseases in the digestive system.
  • Neurological diseases.
  • Malignant diseases in the past or in the present. Treated with chemotherapy or radiation.
  • Genetic syndromes
  • Bone diseases
  • Taking chronic medicine, SSRI type, that effect the appetite and the growth hormone signal transduction.

Treatment and study plan

growth hormone- Genotropin or NorditropinSimplex and nutritional intervention

Behavioral

A combined treatment of growth hormone (Genotropin or NorditropinSimplex or "Biotropin") and nutritional intervention

growth hormone-Genotropin or NorditropinSimplex or "Biotropin"

Behavioral

Growth hormone treatment (Genotropin, or NorditropinSimplex or "Biotropin").

Primary outcomes

  1. height and weight

    Time frame: every visit until the end of study

  2. Growth markers

    Time frame: At screening visit, baseline and at the end of the visit

Secondary outcomes

  1. Safety laboratory parameters

    Time frame: at screening, baseline and at the end of the study

  2. food diary

    Time frame: every visit until the end of the study

  3. Resting energy expenditure measurements

    Time frame: Every visit other than visit number 4

Sponsors and collaborators

Lead sponsor

Rabin Medical Center

Other

Registry information

Official study title

Effects of Growth Hormone Treatment on Eating Regulation and Comparison Between the Growth Responses With or Without Nutritional Intervention in Short Stature Children

Important dates

Study start
2008
Primary completion
2012
Study completion
2012
First posted
Nov 22, 2007
Registry last updated
Jul 16, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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