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NCT00206297 · ClinicalTrials.gov registry record · Phase 3

The Effect of Prolonged Pramlintide Infusion in Pediatric Diabetes

A Phase 3 study of Type 1 Diabetes, sponsored by Baylor College of Medicine.

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

NCT00206297 is a Phase 3 study of Type 1 Diabetes that has completed, run by Baylor College of Medicine. The registered enrollment target is 20 participants, below the 824-participant average among 178 other Type 1 Diabetes trials with a reported enrollment target (98% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT00206297, a Phase 3 study of Type 1 Diabetes, has completed, sponsored by Baylor College of Medicine.

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

Study Summary

The purpose of this study is to see if reducing the dose of insulin before a meal and giving both pramlintide and insulin as dual wave infusions will lower the chance of low blood sugars after a meal. In addition, the study will look at giving pramlintide as a basal infusion (a very low steady dose) for several hours

Conditions Studied

Interventions

  • DRUG Pramlintide

Study Locations (1)

Texas

  • Baylor College of Medicine - Houston

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2003-10
Est. Completion 2006-02
Phase Phase 3

Sponsor

Baylor College of Medicine

616 total trials

What the Registry Record Tells You About NCT00206297

The ClinicalTrials.gov registry entry for NCT00206297 describes a study currently listed as completed, categorized as Phase 3. The registered enrollment target is 20 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 824-participant average among 178 other Type 1 Diabetes trials with a reported enrollment target (98% lower). The listed sponsor is Baylor College of Medicine, which has 616 total studies on file at ClinicalTrials.gov.

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

NCT00206297 reports 1 study location spanning 1 distinct geographic area - top geographies include Texas.

Frequently Asked Questions

What is clinical trial NCT00206297 about?

NCT00206297 is a clinical study titled "The Effect of Prolonged Pramlintide Infusion in Pediatric Diabetes". The purpose of this study is to see if reducing the dose of insulin before a meal and giving both pramlintide and insulin as dual wave infusions will lower the chance of low blood sugars after a meal. In addition, the study will look at giving pramlintide as a basal infusion (a very low steady dose)...

What is the current status of trial NCT00206297?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 20 participants. The study started on 2003-10. Estimated completion is 2006-02.

What conditions does trial NCT00206297 study?

This clinical trial studies the following conditions: Type 1 Diabetes.

What interventions are being tested in trial NCT00206297?

The interventions under investigation include: Pramlintide (DRUG).

Who is sponsoring clinical trial NCT00206297?

This trial is sponsored by Baylor College of Medicine, which has 616 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00206297 being conducted?

This trial has 1 study location across Texas. 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.