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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 is a Phase 1 study that has completed, run by Vanderbilt University Medical Center. The registered enrollment target is 20 participants.

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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.

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 Registry Record Tells You About NCT00574912

The ClinicalTrials.gov registry entry for NCT00574912 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 20 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Vanderbilt University Medical Center, which has 677 total studies on file at ClinicalTrials.gov.

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

NCT00574912 reports 0 study locations.

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.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.