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Sex Differences in Statural Growth Impairment in Pediatric Crohn's Disease (Growth Study)

Published: 09/24/2018

General Information:

National Institutes of Health (NIH) - Turning Discovery into Health
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Study Objective

To investigate the underlying mechanisms of sex differences in statural growth impairment and to develop a predictive model to identify patients at highest risk for developing growth impairment refractory to standard therapeutic approaches

Phase of study
Other
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Eligibility:

Age
Pediatric (under 18)
Gender
Female
Male
Disease Type
crohns-disease
Severity
Mild
Moderate
Severe
Eligibility Criteria

 

Eligibility:

  • Crohn’s disease
  • Males ages 6 to 15 years
  • Females ages 5 to 13 years

Detailed eligibility reviewed when patient contacts the Study Team

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Study Details:

Study Description

 

If the patient is eligible to participate after the Screening Visit, she/he will meet with the Growth Study Team five times over two years (approximately once every 6 months) and do the following:

  • Answer questions about her/his medical history and physical development
  • Get up to 2 more x-rays of her/his left hand to determine her/his bone age (skeletal maturation)
  • Have her/his height and weight measured
  • Have blood drawn
  • Record what she/he eats and drinks (undergo nutrient intake assessment)

OPTIONAL procedures include allowing a doctor to perform a physical exam to stage her/his physical development and allow storage of blood for future testing.

Description of Treatment or Intervention (Mechanism of Action)

 

This is an observational study. No treatment/intervention is involved in this study.

Patient Participation Requirements

Prospective participants are screened for study eligibility. Screening will include answering questions about the participant's medical history and physical development and obtaining an x-ray of her/his left hand to determine bone age. Height and weight measurements will also be obtained. If eligible to participate after the Screening Visit, participants will meet with the Growth Study Team five more times over two years (approximately once every 6 months) and answer questions about her/his medical history and physical development, get up to 2 more x-rays of her/his hand to determine her/his bone age, have her/his height and weight measured, have blood drawn, and record what she/he eats and drinks (undergo nutrient intake assessment). Optional procedures will include allowing a doctor to perform a physical exam to stage her/his physical development and allow storage of blood for future testing and genetic testing. Biological parents will be asked if Study Team can measure their heights once during the study.

Possible Risks & Side Effects

There are no major risks associated with the study.

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Contact Information:

Site Locations

Weill Cornell Medicine 505 E. 70th Street New York, New York 10021
Christina Edwards
646-962-4968
[email protected]
Goryeb Children's Hospital 100 Madison Avenue Morristown, New Jersey 07962
Christina Edwards
646-962-4968
[email protected]
University of North Carolina 333 S. Columbia Street Chapel Hill, North Carolina 27599
Christina Edwards
646-962-4968
[email protected]
University of Chicago Medicine 5841 S. Maryland Avenue Chicago, Illinois 60637
Christina Edwards
646-962-4968
[email protected]
University of Texas Southwestern 1935 Medical District Drive Dallas, Texas 75235
Christina Edwards
646-962-4968
[email protected]
Children's Mercy Hospital in Kansas City 2401 Gillham Road Kansas City, Missouri 64108
Christina Edwards
646-962-4968
[email protected]
Children's Hospital of Pittsburgh of UPM 4401 Penn Avenue Pittsburgh, Pennsylvania 15224
Christina Edwards
646-962-4968
[email protected]
Primary Children's Hospital at Salt Lake City 417 Wakara Way Salt Lake City, Utah 84108
Christina Edwards
646-962-4968
[email protected]
Click Here to Learn More »
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