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NCT00312130 · ClinicalTrials.gov registry record · Phase 3

A Study to Evaluate the Effects of Vildagliptin on the Insulin Response to Glucose in Subjects With Pre-diabetes

A Phase 3 study of PreDiabetes, sponsored by Novartis.

Completed
Registry status
Phase 3
Development phase
20
Enrollment target
1
Study location

NCT00312130: Completed Phase 3 study of PreDiabetes, sponsored by Novartis.

NCT00312130 is a Phase 3 study of PreDiabetes that has completed, run by Novartis. The registered enrollment target is 20 participants, below the 701-participant average among 149 other PreDiabetes trials with a reported enrollment target (97% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00312130, a Phase 3 study of PreDiabetes, has completed, sponsored by Novartis.

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

Study Summary

This is an exploratory study to assess whether vildagliptin, an unapproved drug, can increase insulin secretion in subjects with pre-diabetes who have a defect in the insulin response and elevated levels of fasting glucose.

Conditions Studied

Interventions

  • DRUG Vildagliptin

Study Locations (1)

Washington

  • University of Washington - Seattle

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2005-04
Est. Completion 2006-11
Phase Phase 3
Novartis

265 total trials

What the finished NCT00312130 record still lists

NCT00312130 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 701-participant average among 149 other PreDiabetes trials with a reported enrollment target (97% lower).

The record links to 1 condition, with PreDiabetes appearing as the primary indexed condition, and to 1 intervention - of which Vildagliptin is the first listed.

NCT00312130 reports a single indexed study location in Washington.

Frequently Asked Questions

What is clinical trial NCT00312130 about?

NCT00312130 is a clinical study titled "A Study to Evaluate the Effects of Vildagliptin on the Insulin Response to Glucose in Subjects With Pre-diabetes". This is an exploratory study to assess whether vildagliptin, an unapproved drug, can increase insulin secretion in subjects with pre-diabetes who have a defect in the insulin response and elevated levels of fasting glucose.

What is the current status of trial NCT00312130?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 20 participants. The study started on 2005-04. Estimated completion is 2006-11.

What conditions does trial NCT00312130 study?

This clinical trial studies the following conditions: PreDiabetes.

What interventions are being tested in trial NCT00312130?

The interventions under investigation include: Vildagliptin (DRUG).

Who is sponsoring clinical trial NCT00312130?

This trial is sponsored by Novartis, which has 265 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00312130 being conducted?

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

Similar trials for PreDiabetes

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT00312130's enrollment target sits among peer trials

20 133rd of 149 higher than 10 of 149 other PreDiabetes trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other PreDiabetes 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 NCT00312130, the US trial registry maintained by the National Library of Medicine. NCT00312130 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.