Basal Insulin in the Management of Patients With Diabetic Ketoacidosis (DKA)

This study has been completed.

Study NCT00590044 Information provided by Emory University

First Received: December 28, 2007 Last Updated: May 18, 2009 History of Changes

Study Type:	Interventional
Study Design:	Randomized, Open Label, Parallel Assignment
Condition:	Diabetic Ketoacidosis
Interventions:	Drug: insulin glargine+ glulisine Drug: NPH + Regular insulin

Participant Flow

Show Participant Flow

Baseline Characteristics

Hide Baseline Characteristics

Reporting Groups

	Description
1	Daily insulin glargine (Lantus) + glulisine (Apidra) before meals
2	Split-mixed NPH + Regular insulin twice daily

Baseline Measures

	1	2	Total
Number of Participants [units: participants]	38	36	74
Age [units: participants]
<=18 years	0	0	0
Between 18 and 65 years	38	36	74
>=65 years	0	0	0
Age [units: years] Mean ± Standard Deviation	39 ± 12	38 ± 12	38.5 ± 12
Gender [units: participants]
Female	14	12	26
Male	24	24	48
Region of Enrollment [units: participants]
United States	38	36	74

Outcome Measures

1. Primary:

Mean Daily Blood Glucose Concentration After the Resolution of DKA [ 1 year ]

Show Outcome Measure 1

Serious Adverse Events

Show Serious Adverse Events

Other Adverse Events

Show Other Adverse Events

More Information

Hide More Information

Certain Agreements:

Principal Investigators are NOT employed by the organization sponsoring the study.

There is NOT an agreement between Principal Investigators and the Sponsor (or its agents) that restricts the PI's rights to discuss or publish trial results after the trial is completed.

Limitations and Caveats

Limitations of the study, such as early termination leading to small numbers of participants analyzed and technical problems with measurement leading to unreliable or uninterpretable data
No text entered.

Results Point of Contact:

Name/Title: Guillermo Umpierrez
Organization: Emory University SOM
phone: 4047781663
e-mail: geumpie@emory.edu

No publications provided

Responsible Party:	Emory Univ SOM ( Guillermo Umpierrez, MD/Principal Investigator )
Study ID Numbers:	790-2006
Study First Received:	December 28, 2007
Results First Received:	January 30, 2009
Last Updated:	May 18, 2009
ClinicalTrials.gov Identifier:	NCT00590044 History of Changes
Health Authority:	United States: Institutional Review Board