Personalizing treatment targets for IGF-1 in Pediatric Growth Hormone Deficient Patients
Summary
Understanding how individual patients respond to treatment is the heart of personalized medicine. This study aims to understand how Insulin-like Growth Factor 1 (IGF-1), a marker of Growth Hormone function in the body, may be used to help determine how patients with Growth Hormone Deficiency are responding to treatment early on.
Eligibility
Eligible ages: 1 to 18
Inclusion criteria:
This study is open to any patients from ages 1 to 18 who are diagnosed with Growth Hormone Deficiency or short stature.
Exclusion criteria:
1) Patients with kidney failure
2) Liver disease
3) Growth hormone resistance
4) Genetic syndromes that are known to be associated with short stature (e.g. Prader Willi or Turner Syndrome)
Participate
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Additional information
Contact information
Dennis Orton, PhD FCACB Clinical Assistant Professor | University of Calgary
Principal investigator:
Dennis Orton
Clinical trial:
No
REB-ID:
REB21-0109