Completed

Assessment of Hippocampal Volume and Memory Function in Cushing's Syndrome

0 criteria met from your profileSee at a glance how your profile meets each eligibility criteria.
Study Aim

This study aims to observe and understand the relationship between hippocampal volume and memory function in individuals diagnosed with Cushing's Syndrome.

What is being collected

Data Collection

Who is being recruted

Adrenal Gland Diseases+5

+ Adrenocortical Hyperfunction

+ Pathologic Processes

From 15 to 80 Years
See all eligibility criteria
How is the trial designed

Observational
Study Start: August 1994
See protocol details

Summary

Principal SponsorNational Center for Research Resources (NCRR)
Last updated: June 24, 2005
Sourced from a government-validated database.Claim as a partner

Study start date: August 1, 1994

Actual date on which the first participant was enrolled.

PROTOCOL OUTLINE: Patients undergo a psychiatric evaluation for mood and cognition during confirmation of diagnosis. Neuropsychologic exams include pencil and paper test and a cognitive assessment. Endocrine studies include dexamethasone and corticotropin-releasing hormone stimulation tests. The hippocampal complex volume is assessed with coronal magnetic resonance imaging. There is a follow-up 1 year after the initiation of treatment.

NCT00004326
Principal SponsorNational Center for Research Resources (NCRR)
Last updated: June 24, 2005
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

12 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

From 15 to 80 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Adrenal Gland DiseasesAdrenocortical HyperfunctionPathologic ProcessesPathological Conditions, Signs and SymptomsDisease AttributesCushing SyndromeEndocrine System DiseasesRare Diseases

Criteria

PROTOCOL ENTRY CRITERIA: Adults and teenagers with untreated, spontaneous active Cushing's syndrome Diagnosis verified at the University of Michigan Medical Center, including the following: Excessive cortisol secretion measured by urinary-free cortisol, cortisol secretion rate, and plasma cortisol level Lack of normal circadian cortisol secretion and failure to suppress following 2 mg of dexamethasone

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

University of Michigan Health Systems

Ann Arbor, United StatesOpen University of Michigan Health Systems in Google Maps
CompletedOne Study Center