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NCT00574912 · ClinicalTrials.gov registry record · Phase 1

Characteristics of Glargine in Type 2 Diabetics

A Phase 1 study, sponsored by Vanderbilt University Medical Center.

Completed
Registry status
Phase 1
Development phase
20
Enrollment target

NCT00574912: Completed Phase 1 study, sponsored by Vanderbilt University Medical Center.

NCT00574912 is a Phase 1 study that has completed, run by Vanderbilt University Medical Center. The registered enrollment target is 20 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (67% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00574912, a Phase 1 study, has completed, sponsored by Vanderbilt University Medical Center.

COMPLETED
Registry status
Phase 1
Development phase
20 participants
Enrollment target

Study Summary

The study is to determine the dose response relationship of insulin glargine in type 2 diabetes over a 24-hour period and measuring the differences in glucose production among the differing doses of glargine. Hypothesis: Differing doses of insulin glargine over a 24-hour period in type 2 diabetes will show differing effects on endogenous glucose production, glucose disposal and carbohydrate and lipid flux.

Primary Outcome

measuring the changes in glucose infusion rate during the 24 hour experimental period.

Interventions

  • DRUG Placebo
  • DRUG Insulin Glargine 0.5 u/kg body wt SC
  • DRUG Insulin Glargine 1.0 u/kg body wt SC
  • DRUG Insulin Glargine 1.5 u/kg body wt SC
  • DRUG Insulin Glargine 2.0 u/kg body wt SC

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2007-03
Est. Completion 2010-01
Phase Phase 1

What the finished NCT00574912 record still lists

NCT00574912 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 20 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (67% lower).

The record links to 0 conditions, and to 5 interventions - of which Placebo is the first listed.

NCT00574912 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00574912 about?

NCT00574912 is a clinical study titled "Characteristics of Glargine in Type 2 Diabetics". The study is to determine the dose response relationship of insulin glargine in type 2 diabetes over a 24-hour period and measuring the differences in glucose production among the differing doses of glargine. Hypothesis: Differing doses of insulin glargine over a 24-hour period in type 2 diabetes w...

What is the current status of trial NCT00574912?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 20 participants. The study started on 2007-03. Estimated completion is 2010-01.

What interventions are being tested in trial NCT00574912?

The interventions under investigation include: Placebo (DRUG), Insulin Glargine 0.5 u/kg body wt SC (DRUG), Insulin Glargine 1.0 u/kg body wt SC (DRUG), Insulin Glargine 1.5 u/kg body wt SC (DRUG), Insulin Glargine 2.0 u/kg body wt SC (DRUG).

Who is sponsoring clinical trial NCT00574912?

This trial is sponsored by Vanderbilt University Medical Center, which has 677 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00574912's enrollment target sits among peer trials

20 1629th of 2000 higher than 285 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 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 NCT00574912, the US trial registry maintained by the National Library of Medicine. NCT00574912 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.