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Insulin Sensitivity and Substrate Metabolism Before and After Treatment in Patients With Growth Hormone Deficiency

Insulin Sensitivity and Substrate Metabolism Before and After Treatment in Patients With Growth Hormone Deficiency

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00646815
Enrollment
24
Registered
2008-03-31
Start date
2008-03-31
Completion date
2009-09-30
Last updated
2009-10-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Growth Hormone Deficiency

Keywords

insulin sensitivity, substrate metabolism, fatty liver, intramyocellular lipids, growth hormone deficiency, Growth hormone deficiency (Adult)

Brief summary

The purpose of this study is to further characterize the treatment related changes in insulin sensitivity, substrate metabolism and intrahepatic-intramyocellular lipids in patients with growth hormone deficiency (GHD).

Interventions

Dosage regulation will follow the local recommendations of GHD treatment

Sponsors

Aarhus University Hospital
CollaboratorOTHER
University of Aarhus
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* Written informed consent * Must be of legal age and competent * Age: \>18 and \<60 years old * Presently diagnosed with growth hormone deficiency; if panhypopituitary, the patient must be sufficiently substituted in the other axis´s, for at least 3 months before inclusion in the study

Exclusion criteria

* Alcohol consumption \>21 units per week * Malignant disease * Pregnancy * Magnetic implants or material in the body * Claustrophobia * BMI \>30 * Heart disease (NYHA \>2) * Uncontrolled hypertension * Manifest diabetes mellitus * Change in medication, with any influence on glucose metabolism, 2 months prior to and until the end of the trial. Controls are matched on age, gender and BMI Inclusion Criteria: * Written informed consent * Must be of legal age and competent

Design outcomes

Primary

MeasureTime frame
insulin sensitivitybefore and after 3 months treatment with growth hormone

Secondary

MeasureTime frame
substrate metabolismbefore and after 3 months of growth hormone treatment
intrahepatic lipid contentbefore and after 3 months of growth hormone treatment
intramyocellular lipid contentbefore and after 3 months of growth hormone treatment

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026