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NCT02785133 · ClinicalTrials.gov registry record · NA

Safety and Feasibility of Polychromatic Light Emitting Diode for Peripheral Catheter Illumination During Peripheral Intravenous Delivery of Normal Saline

A NA study of Fatigue and Quality of Life, sponsored by UVLrx Therapeutics.

Completed
Registry status
NA
Development phase
3,063
Enrollment target
1
Study location

NCT02785133 is a NA study of Fatigue and Quality of Life that has completed, run by UVLrx Therapeutics. The registered enrollment target is 3,063 participants, above the 190-participant average among 109 other Fatigue trials with a reported enrollment target (1512% higher). The trial reports 1 study location across 1 state.

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The verdict

NCT02785133, a NA study of Fatigue and Quality of Life, has completed, sponsored by UVLrx Therapeutics.

COMPLETED
Registry status
NA
Development phase
3,063 participants
Enrollment target
1
Study location

Study Summary

This study uses a prospective non-randomized, non-controlled design. Five-hundred (500) subjects having previously received a peripheral intravenous therapy will be enrolled into a single treatment group. The purpose of the study is to evaluate the safety, feasibility, and improved energy levels following treatment with a low-light source integrated into an existing peripheral intravascular catheter. The absence of a control group is based on the following reason:This is a pilot investigation to establish a baseline understanding of the safety, feasibility, and cursory utility of polychromatic light emitting diodes integrated into an existing 20-gauge 1.0 inch intravenous catheter to improve self-reported overall subject energy levels.

Conditions Studied

Interventions

  • DEVICE UVL1000 Treatment Station
  • DRUG Normal Saline Solution
  • DEVICE Peripheral Catheterization

Study Locations (1)

Texas

  • Lozano Medical Clinic - Dallas

Trial Details

FieldValue
Enrollment Target 3,063 participants
Start Date 2014-12
Est. Completion 2016-10
Phase NA

Sponsor

UVLrx Therapeutics

1 total trials

What the Registry Record Tells You About NCT02785133

The ClinicalTrials.gov registry entry for NCT02785133 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 3,063 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 190-participant average among 109 other Fatigue trials with a reported enrollment target (1512% higher). The listed sponsor is UVLrx Therapeutics, which has 1 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Fatigue appearing as the primary indexed condition, and to 3 interventions - of which UVL1000 Treatment Station is the first listed.

NCT02785133 reports 1 study location spanning 1 distinct geographic area - top geographies include Texas.

Frequently Asked Questions

What is clinical trial NCT02785133 about?

NCT02785133 is a clinical study titled "Safety and Feasibility of Polychromatic Light Emitting Diode for Peripheral Catheter Illumination During Peripheral Intravenous Delivery of Normal Saline". This study uses a prospective non-randomized, non-controlled design. Five-hundred (500) subjects having previously received a peripheral intravenous therapy will be enrolled into a single treatment group. The purpose of the study is to evaluate the safety, feasibility, and improved energy levels fol...

What is the current status of trial NCT02785133?

This trial is currently completed. It is a NA study. The enrollment target is 3,063 participants. The study started on 2014-12. Estimated completion is 2016-10.

What conditions does trial NCT02785133 study?

This clinical trial studies the following conditions: Fatigue, Quality of Life.

What interventions are being tested in trial NCT02785133?

The interventions under investigation include: UVL1000 Treatment Station (DEVICE), Normal Saline Solution (DRUG), Peripheral Catheterization (DEVICE).

Who is sponsoring clinical trial NCT02785133?

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

Where is trial NCT02785133 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

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