Diagnostic Performance of Screening Tests for Cushing s Syndrome
NCT00361777 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 471
Last updated 2019-12-16
Summary
This study will test the accuracy of screening tests for Cushing s syndrome in overweight people with signs of the disorder. Cushing s syndrome is a rare disorder caused by excess production of the hormone cortisol. Patients may have various problems, such as weight gain, high blood pressure, diabetes, infections, mood problems, trouble concentrating, and increased blood clotting. These symptoms are seen in many other disorders as well, complicating the diagnosis. The reliability of tests currently used to diagnose Cushing s syndrome is not known. To test their accuracy, subjects in this study who test positive for Cushing s syndrome will be evaluated at NIH for 2 years to either confirm or refute the laboratory results.
Patients between 18 and 75 years of age who are being treated at the George Washington University Weight Management Program (GWUWMP) may participate in this study. Candidates will be screened with a medical history, physical examination, measurement of body fat, blood tests, and oral glucose tolerance test. They will also complete a symptoms checklist and quality of life questionnaire.
Participants will be tested for Cushing s syndrome with a saliva collection, 24-hour urine collection, and dexamethasone suppression test (DST). For the DST they will take 1 mg of dexamethasone at night and report to GWUWMP the next morning for a blood draw. All specimens blood, saliva, and urine will be tested for cortisol levels.
People whose test results are abnormal will be seen at the NIH outpatient clinic for a medical history, physical examination, and blood tests; bedtime saliva collection; two 24-hour urine collections; and a 2-day 2-mg DST, followed by administration of corticotropin-releasing hormone (CRH). CRH is a naturally occurring hormone that causes cortisol levels to rise. Pre-treatment with dexamethasone prevents CRH from causing an increase in cortisol in healthy people, but not in patients with Cushing s syndrome. For the 2-day DST, the subject takes 0.5 mg dexamethasone every 6 hours for eight doses. Two hours after the last dose, CRH is injected through a catheter (thin plastic tube) inserted into an arm vein. Blood is drawn just before giving CRH to measure dexamethasone and cortisol levels and after giving CRH to measure cortisol levels.
People whose test results are normal will not be seen further at NIH. Those with high cortisol levels will have repeat urine and saliva tests every 2 to 8 weeks for up to 24 months, and a 1-mg DST every 3 months during routine clinic visits at GWUWMP. People whose increased cortisol is found to be due to another condition besides Cushing s syndrome will be referred for evaluation and possible treatment. Those diagnosed with Cushing s syndrome will have standard tests to identify the tumor causing the disorder, followed by standard medical and surgical treatment.
Conditions
Sponsors & Collaborators
-
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
lead NIH
Principal Investigators
-
Lynnette K Nieman, M.D. · National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Eligibility
- Min Age
- 18 Years
- Max Age
- 100 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2002-09-19
- Completion
- 2019-10-30
Countries
- United States
Study Locations
More Related Trials
-
Study of Adrenal Gland Tumors
NCT00005927 ·Status: COMPLETED
-
Steroid Panel for One-step Diagnosis of Adrenal Diseases
NCT04948970 ·Status: COMPLETED
-
Cortisol Activity in Patients With Prader-Willi Syndrome and Healthy Controls
NCT00932932 ·Status: COMPLETED
-
Adrenocorticotropic Hormone Stimulation in Postural Orthostatic Tachycardia Syndrome (POTS)
NCT01764711 ·Status: COMPLETED ·Phase: NA
-
Study of UK Adults With Congenital Adrenal Hyperplasia.
NCT00749593 ·Status: COMPLETED
-
Corticosteroids in Postoperative Critically Ill Neonates With Low Cardiac Output Syndrome With Congenital Heart Disease
NCT00590018 ·Status: COMPLETED ·Phase: PHASE2
-
Diagnosis of Central Adrenal Insufficiency in Patients With Prader-Willi Syndrome
NCT02368379 ·Status: COMPLETED ·Phase: NA
-
Diagnosis of Pheochromocytoma
NCT00004847 ·Status: RECRUITING ·Phase: PHASE1
-
Comparison of Continuous Non-Invasive and Invasive Intracranial Pressure Measurement
NCT01863381 ·Status: TERMINATED ·Phase: NA
-
Detecting Mild Autonomous Cortisol Secretion in Patients With Adrenal Incidentaloma
NCT06344143 ·Status: RECRUITING
-
Use of Copeptin in Diabetes Insipidus
NCT01940614 ·Status: COMPLETED
-
Examining Genetic Differences Among People With 21-Hydroxylase Deficiency
NCT00542841 ·Status: COMPLETED ·Phase: NA
-
Diet as a Potential Treatment for Autosomal Dominant Polycystic Kidney Disease
NCT02225860 ·Status: COMPLETED ·Phase: PHASE2/PHASE3
-
Tilt Table With Suspected Postural Orthostatic Tachycardia Syndrome (POTS) Subjects
NCT01617616 ·Status: COMPLETED
-
Study of Alpha-blockers Alone During Preoperative Preparation in Patients With Pheochromocytoma
NCT05803330 ·Status: COMPLETED ·Phase: NA
-
Assessment of ShuntCheck Performance Characteristics in Asymptomatic Patients With Normal Pressure Hydrocephalus
NCT04011566 ·Status: RECRUITING
-
Extreme Morphology and Metabolic Health
NCT05991609 ·Status: ACTIVE_NOT_RECRUITING
-
Study of Skeletal Disorders
NCT05031507 ·Status: RECRUITING
-
Biomarkers for Feeding Intolerance in Infants With Complex Congenital Heart Defects Undergoing Single Ventricle Staged Palliation
NCT02995577 ·Status: UNKNOWN
-
Incidence of cCPHD in Denmark - a National Observational Study
NCT05334563 ·Status: UNKNOWN
-
Implementation of a Diagnostic Workflow for Personalized Diagnosis of Nephrotic Syndrome
NCT06325098 ·Status: RECRUITING ·Phase: NA
-
Cardiac Function and Morphology Evaluated by Magnetic Resonance Imaging in Growth Hormone Deficiency and Acromegaly
NCT00970463 ·Status: COMPLETED
-
Metabolic Derangements in Acute Heart Failure Syndrome
NCT00682175 ·Status: TERMINATED
-
Early-onset Obesity and Cognitive Impairment in Children With Pseudohypoparathyroidism
NCT02411461 ·Status: COMPLETED
-
Prognostic Value of Transforming Growth Factor-Beta 1 in Normal Pressure Hydrocephalus
NCT00600795 ·Status: COMPLETED