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NCT00065130 · ClinicalTrials.gov registry record · Phase 3

Safety and Efficacy of Insulin Aspart vs. Regular Human Insulin in Gestational Diabetes

A Phase 3 study of Diabetes and Gestational Diabetes, sponsored by Novo Nordisk A/S.

Completed
Registry status
Phase 3
Development phase
27
Enrollment target
1
Study location

NCT00065130 is a Phase 3 study of Diabetes and Gestational Diabetes that has completed, run by Novo Nordisk A/S. The registered enrollment target is 27 participants, below the 3,028-participant average among 338 other Diabetes trials with a reported enrollment target (99% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT00065130, a Phase 3 study of Diabetes and Gestational Diabetes, has completed, sponsored by Novo Nordisk A/S.

COMPLETED
Registry status
Phase 3
Development phase
27 participants
Enrollment target
1
Study location

Study Summary

This trial is conducted in the United States of America (USA). The purpose of this study is to test whether NovoLog (insulin aspart) is a safe and at least as effective alternative to regular human insulin for the control of blood glucose after meals in women who develop diabetes during pregnancy.

Interventions

  • DRUG insulin aspart
  • DRUG insulin NPH
  • DRUG human insulin

Study Locations (1)

California

  • Novo Nordisk Investigational Site - Santa Barbara

Trial Details

FieldValue
Enrollment Target 27 participants
Start Date 2000-04
Est. Completion 2003-12
Phase Phase 3

Sponsor

Novo Nordisk A/S

431 total trials

What the Registry Record Tells You About NCT00065130

The ClinicalTrials.gov registry entry for NCT00065130 describes a study currently listed as completed, categorized as Phase 3. The registered enrollment target is 27 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 3,028-participant average among 338 other Diabetes trials with a reported enrollment target (99% lower). The listed sponsor is Novo Nordisk A/S, which has 431 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Diabetes appearing as the primary indexed condition, and to 3 interventions - of which insulin aspart is the first listed.

NCT00065130 reports 1 study location spanning 1 distinct geographic area - top geographies include California.

Frequently Asked Questions

What is clinical trial NCT00065130 about?

NCT00065130 is a clinical study titled "Safety and Efficacy of Insulin Aspart vs. Regular Human Insulin in Gestational Diabetes". This trial is conducted in the United States of America (USA). The purpose of this study is to test whether NovoLog (insulin aspart) is a safe and at least as effective alternative to regular human insulin for the control of blood glucose after meals in women who develop diabetes during pregnancy.

What is the current status of trial NCT00065130?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 27 participants. The study started on 2000-04. Estimated completion is 2003-12.

What conditions does trial NCT00065130 study?

This clinical trial studies the following conditions: Diabetes, Gestational Diabetes.

What interventions are being tested in trial NCT00065130?

The interventions under investigation include: insulin aspart (DRUG), insulin NPH (DRUG), human insulin (DRUG).

Who is sponsoring clinical trial NCT00065130?

This trial is sponsored by Novo Nordisk A/S, which has 431 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00065130 being conducted?

This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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

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.