Disorders of Systemic Glucose Balance - Tabular View

This Tabular View shows the required WHO registration data elements as marked by ^†

Tracking Information
First Received Date ^†	November 18, 2000
Last Updated Date	June 23, 2005
Start Date ^†
Current Primary Outcome Measures ^†
Original Primary Outcome Measures ^†
Change History	Complete list of historical versions of study NCT00006508 on ClinicalTrials.gov Archive Site
Current Secondary Outcome Measures ^†
Original Secondary Outcome Measures ^†

Descriptive Information
Brief Title ^†	Disorders of Systemic Glucose Balance
Official Title ^†
Brief Summary	We wish to identify people with hypoglycemia (low blood sugar) and ultimately determine why the blood sugar levels are so low. To do so, we will contrast the responses of patients suspected to have hypoglycemia with those of healthy subjects during standardized tests. Those tests may include: 1) a controlled hypoglycemia produced by administration of insulin, a blood sugar-lowering hormone, and sugar, 2) a formula meal, and 3) a period of up to 72 hours without food.
Detailed Description
Study Phase
Study Type ^†	Interventional
Study Design ^†	Diagnostic
Condition ^†	Hypoglycemia
Intervention ^†	Procedure: Controlled hypoglycemia using insulin Procedure: formula meal
Study Arms / Comparison Groups
Publications *
* Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.

Recruitment Information
Recruitment Status ^†	Completed
Enrollment ^†
Completion Date
Primary Completion Date
Eligibility Criteria ^†	Inclusion Criteria: Patients with suspected hypoglycemia Healthy subjects (controls) Absence of known macrovascular disease or of known CNS disease by medical history, physical examination or ECG (exclusions for induced hypoglycemia) Ability to give informed consent
Gender	Both
Ages	18 Years and older
Accepts Healthy Volunteers	Yes
Contacts ^††
Location Countries ^†	United States
Expanded Access Status

Administrative Information
NCT ID ^†	NCT00006508
Responsible Party
Secondary IDs ^††	M01RR00036
Study Sponsor ^†	National Center for Research Resources (NCRR)
Collaborators ^††
Investigators ^†
Information Provided By	National Center for Research Resources (NCRR)
Verification Date	December 2003
^† Required WHO trial registration data element. ^†† WHO trial registration data element that is required only if it exists.