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NCT00935909 · ClinicalTrials.gov registry record

Use of Vein Viewer for Insertion of Peripheral Venous Cannula in Pediatric Patients With Difficult Intravenous Access

A clinical trial of IV Cannulation, sponsored by Peter Szmuk.

Completed
Registry status
603
Enrollment target
1
Study location

NCT00935909 is a study of IV Cannulation that has completed, run by Peter Szmuk. The registered enrollment target is 603 participants. The trial reports 1 study location across 1 state.

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The verdict

NCT00935909, a study of IV Cannulation, has completed, sponsored by Peter Szmuk.

COMPLETED
Registry status
603 participants
Enrollment target
1
Study location

Study Summary

The primary purpose of this prospective, randomized trial is successful intravenous (IV) cannulation on first attempt with the use of either the Vein Viewer (VV) or standard cannulation method. The secondary purpose is to find out if there is a difference in the total time to successful cannulation.

Conditions Studied

Study Locations (1)

Texas

  • Children's Medical Center Dallas - Dallas

Trial Details

FieldValue
Enrollment Target 603 participants
Start Date 2009-01
Est. Completion 2010-07

Sponsor

Peter Szmuk

1 total trials

What the Registry Record Tells You About NCT00935909

The ClinicalTrials.gov registry entry for NCT00935909 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 603 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Peter Szmuk, which has 1 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with IV Cannulation appearing as the primary indexed condition, and to 0 interventions.

NCT00935909 reports 1 study location spanning 1 distinct geographic area - top geographies include Texas.

Frequently Asked Questions

What is clinical trial NCT00935909 about?

NCT00935909 is a clinical study titled "Use of Vein Viewer for Insertion of Peripheral Venous Cannula in Pediatric Patients With Difficult Intravenous Access". The primary purpose of this prospective, randomized trial is successful intravenous (IV) cannulation on first attempt with the use of either the Vein Viewer (VV) or standard cannulation method. The secondary purpose is to find out if there is a difference in the total time to successful cannulation.

What is the current status of trial NCT00935909?

This trial is currently completed. The enrollment target is 603 participants. The study started on 2009-01. Estimated completion is 2010-07.

What conditions does trial NCT00935909 study?

This clinical trial studies the following conditions: IV Cannulation.

Who is sponsoring clinical trial NCT00935909?

This trial is sponsored by Peter Szmuk, which has 1 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00935909 being conducted?

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

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.