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NCT00590044 · ClinicalTrials.gov registry record · Phase 4

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

A Phase 4 study, sponsored by Emory University.

Completed
Registry status
Phase 4
Development phase
74
Enrollment target

NCT00590044: Completed Phase 4 study, sponsored by Emory University.

NCT00590044 is a Phase 4 study that has completed, run by Emory University. The registered enrollment target is 74 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (86% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00590044, a Phase 4 study, has completed, sponsored by Emory University.

COMPLETED
Registry status
Phase 4
Development phase
74 participants
Enrollment target

Study Summary

The study is a multicenter, randomized controlled trial to compare the safety and efficacy of insulin analogs and human insulins both during acute intravenous treatment and during the transition to subcutaneous insulin in patients with diabetic ketoacidosis (DKA).

Primary Outcome

To determine the safety of the two treatments the number of hypoglycemia episodes that occurred between the 2 groups are measured from the time of transitioning to subcutaneous insulin to day 5. The hypoglycemia events are defined as blood glucose levels \<70 mg/dL. The results were obtained from the citation Umpierrez GE, Jones S, Smiley D, Mulligan P, Keyler T, Temponi A, Semakula C, Umpierrez D, Peng L, Cerón M, Robalino G. Insulin analogs versus human insulin in the treatment of patients wit

Interventions

  • DRUG insulin glargine+ glulisine
  • DRUG NPH + Regular insulin

Trial Details

FieldValue
Enrollment Target 74 participants
Start Date 2007-12
Est. Completion 2008-08
Phase Phase 4
Emory University

1,208 total trials

What the finished NCT00590044 record still lists

NCT00590044 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 74 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (86% lower).

The record links to 0 conditions, and to 2 interventions - of which insulin glargine+ glulisine is the first listed.

NCT00590044 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00590044 about?

NCT00590044 is a clinical study titled "Basal Insulin in the Management of Patients With Diabetic Ketoacidosis (DKA)". The study is a multicenter, randomized controlled trial to compare the safety and efficacy of insulin analogs and human insulins both during acute intravenous treatment and during the transition to subcutaneous insulin in patients with diabetic ketoacidosis (DKA).

What is the current status of trial NCT00590044?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 74 participants. The study started on 2007-12. Estimated completion is 2008-08.

What interventions are being tested in trial NCT00590044?

The interventions under investigation include: insulin glargine+ glulisine (DRUG), NPH + Regular insulin (DRUG).

Who is sponsoring clinical trial NCT00590044?

This trial is sponsored by Emory University, which has 1,208 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00590044's enrollment target sits among peer trials

74 1027th of 2000 higher than 968 of 2,000 other Phase 4 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 4 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00590044, the US trial registry maintained by the National Library of Medicine. NCT00590044 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.