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Clinical Trials/NCT00711061
NCT00711061
Completed
Not Applicable

Cardiovascular Risk in Growth Hormone Deficient Young Adult Males After Completing Growth Hormone Therapy.

Children's Mercy Hospital Kansas City1 site in 1 country24 target enrollmentJune 2008

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Growth Hormone Deficiency
Sponsor
Children's Mercy Hospital Kansas City
Enrollment
24
Locations
1
Primary Endpoint
Compare carotid artery intima medial thickness
Status
Completed
Last Updated
17 years ago

Overview

Brief Summary

The purpose of this study is to compare the cardiovascular risks of growth hormone deficient young adult males who have completed growth hormone therapy to healthy young adult males.

Detailed Description

Adults with growth hormone deficiency are at risk for cardiovascular disease. What age this begins is not known. The objectives of this study are to compare the following measurements between growth hormone deficient young males 3-7 years post completion of growth hormone treatment and age related healthy controls: 1. Carotid artery imaging 2. Metabolic and cardiac parameters 3. Body composition measurements

Registry
clinicaltrials.gov
Start Date
June 2008
End Date
February 2009
Last Updated
17 years ago
Study Type
Observational
Sex
Male

Investigators

Sponsor
Children's Mercy Hospital Kansas City

Eligibility Criteria

Inclusion Criteria

  • Males, 18-25 years old
  • Completed growth hormone therapy approximately 3-5 years prior to study enrollment
  • History of multiple pituitary hormone deficiencies or growth hormone stimulation test \<7 at initiation of growth hormone therapy
  • Healthy Control Inclusion Criteria:
  • Males, 18-25 years old
  • No confirmed endocrine diagnosis including Diabetes and thyroid disorders
  • BMI - z-score within 2 SD of mean

Exclusion Criteria

  • Known risk factors for cardiovascular disease (eg tobacco use, hypertension, diabetes)
  • Family history of early cardiovascular disease (myocardial infarction or stroke \<55years of age) in first degree family members
  • Any implanted device
  • Medication known to interfere with glucose or lipid metabolism or to influence blood pressure
  • Chronic organ illness (eg severe asthma, hepatic or nephritic conditions)

Outcomes

Primary Outcomes

Compare carotid artery intima medial thickness

Time Frame: During study visit

Secondary Outcomes

  • Compare metabolic parameters and body composition measurements(During study visit)

Study Sites (1)

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