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Counterregulatory Hormone Production in Adrenal Insufficiency and Diabetes Type I

Counterregulatory Hormone Production and Cognitive Function in Patients With Adrenal Insufficiency and Diabetes Mellitus Type I

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01452893
Acronym
CANDI
Enrollment
40
Registered
2011-10-17
Start date
2011-03-31
Completion date
2013-12-31
Last updated
2014-01-06

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

Conditions

Addison's Disease, Adrenal Insufficiency, Diabetes Mellitus Type I

Brief summary

Patients with adrenal insufficiency also exhibit an adrenomedullary dysfunction. Furthermore, patients who suffer from both, adrenal insufficiency and type I diabetes more frequently report hypoglycemia, particularly after strenuous activities. The study investigates the counter regulatory hormonal response to physical stress and the impact on cognitive function in subjects with and without Addison's disease, type I diabetes and healthy subjects.

Detailed description

As patients with adrenal insufficiency also exhibit an adrenomedullary dysfunction and patients who suffer from both, adrenal insufficiency and type I diabetes more frequently report hypoglycemia, particularly after strenuous activities this study investigates the counter-regulatory hormonal response to physical stress and the impact on cognitive function in subjects with and without Addison's disease, type I diabetes and healthy subjects. Patients will perform ergometer training with an individualized intensity and fulfill cognitive function testing (stroop test and fatigue inventories) before and after strenuous activity.

Interventions

At visit 1 determination of the individual VO2max (maximal oxygen uptake) by spiroergometry after first testing of cognitive function. At visit 2: Spiroergometry with 3 min warm up followed by 5 min 50% VO2max and 15 min at the individual respiratory compensation point (RCP).

Sponsors

University of Wuerzburg
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Diagnosis of Addison's disease and/or diabetes mellitus type I or healthy control with normal adrenal function and normal glucose regulation * Age ≥ 18 years * Ability to comply with the study protocol * Capability to perform spiroergometry

Exclusion criteria

* Any contraindication for performing spiroergometry according to the guidelines of the German Cardiac Society: * acute myocardial infarction * instable angina pectoris * symptomatic arrhythmia * severe and symptomatic stenosis of the aortic valve * decompensated heart failure * acute pulmonary embolism * Acute myocarditis * Acute pericarditis * Acute aortic dissection * main coronary artery disease * valvulopathies * electrolyte disturbance * arterial hypertension (systolic blood pressure \> 200 mm Hg, diastolic BP \> 110 mm Hg) * Tachyarrhythmia or Bradyarrhythmia * Hypertrophic cardiomyopathy and other forms of obstructive heart disease * second or third degree atrioventricular block * Fever * Diabetes mellitus Type 2 * Diseases or medication influencing the endogenous levels of plasma catecholamines(e. g. pheochromocytoma, paraganglioma, antidepressants, levodopa) * Glucocorticoid-pharmacotherapy

Design outcomes

Primary

MeasureTime frameDescription
difference in cognitive function before and after physical stresstesting is performed at first visit (baseline, duration 5 min) and second visit (at least 48 hours after visit1). The second test is performed 5 min after strenous activity of 23 min duration, test duration again 5 min)study participants are tested with three standardized tests: stroop-task, symptom rating scale and a short term memory test. First testing is performed at visit 1 at rest, the second test at visit 2 after strenuous activity at a bicycle ergometer.

Secondary

MeasureTime frameDescription
differences in counterregulatory hormonal response to physical stressat visit 2, blood sampling over 180 min starting 10 min before spiroergometryblood samples for determination of blood glucose, catecholamines and other counterregulatory hormones (cortisol, growth hormone) are collected before, during and after physical activity.

Countries

Germany

Outcome results

None listed

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