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NCT00920725 · ClinicalTrials.gov registry record · NA

Subcutaneous Aspart Insulin to Treat Diabetic Ketoacidosis (DKA) and Beta-Hydroxybutyrate Testing in DKA

A NA study, sponsored by Rush University Medical Center.

Completed
Registry status
NA
Development phase
50
Enrollment target

NCT00920725: Completed NA study, sponsored by Rush University Medical Center.

NCT00920725 is a NA study that has completed, run by Rush University Medical Center. The registered enrollment target is 50 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00920725, a NA study, has completed, sponsored by Rush University Medical Center.

COMPLETED
Registry status
NA
Development phase
50 participants
Enrollment target

Study Summary

The purpose of this study is to determine whether insulin administered by a subcutaneous injection is effective in the treatment of a diabetic crisis and to determine if beta-hydroxybutyrate is useful to monitor during treatment of a diabetic crisis.

Interventions

  • DRUG Insulin (Aspart Insulin [Novolog], Regular Insulin)

Trial Details

FieldValue
Enrollment Target 50 participants
Start Date 2005-01
Est. Completion 2007-12
Phase NA
Rush University Medical Center

320 total trials

What the finished NCT00920725 record still lists

NCT00920725 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 50 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower).

The record links to 0 conditions, and to 1 intervention - of which Insulin (Aspart Insulin [Novolog], Regular Insulin) is the first listed.

NCT00920725 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00920725 about?

NCT00920725 is a clinical study titled "Subcutaneous Aspart Insulin to Treat Diabetic Ketoacidosis (DKA) and Beta-Hydroxybutyrate Testing in DKA". The purpose of this study is to determine whether insulin administered by a subcutaneous injection is effective in the treatment of a diabetic crisis and to determine if beta-hydroxybutyrate is useful to monitor during treatment of a diabetic crisis.

What is the current status of trial NCT00920725?

This trial is currently completed. It is a NA study. The enrollment target is 50 participants. The study started on 2005-01. Estimated completion is 2007-12.

What interventions are being tested in trial NCT00920725?

The interventions under investigation include: Insulin (Aspart Insulin [Novolog], Regular Insulin) (DRUG).

Who is sponsoring clinical trial NCT00920725?

This trial is sponsored by Rush University Medical Center, which has 320 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00920725's enrollment target sits among peer trials

50 1279th of 2000 higher than 622 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA 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 NCT00920725, the US trial registry maintained by the National Library of Medicine. NCT00920725 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.