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NCT01714063 · ClinicalTrials.gov registry record

Drug Delivery Via Pressurized Metered-dose Inhaler and Valved Holding Chamber in Asthmatic Children: Determination of Delivered Dose Following Coordinated and Uncoordinated Use

A clinical trial, sponsored by Philips Respironics.

Completed
Registry status
34
Enrollment target

NCT01714063: Completed study, sponsored by Philips Respironics.

NCT01714063 is a clinical trial that has completed, run by Philips Respironics. The registered enrollment target is 34 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01714063 has completed, sponsored by Philips Respironics.

COMPLETED
Registry status
34 participants
Enrollment target

Study Summary

The primary objective of this study is to determine ex vivo the amount of fluticasone deposited onto a filter (delivered dose) interposed between the OptiChamber Diamond Valved Holding Chamber (VHC) mouthpiece and the subject's mouth during coordinated and uncoordinated actuation/inhalation maneuver.

Primary Outcome

This is a measure of the the amount of fluticasone deposited onto a filter (delivered dose) during coordinated and uncoordinated actuation/inhalation maneuver. The coordinated maneuver occurs when the firing of the fluticasone is coordinated with the inhalation of the patient . An uncoordinated maneuver occurs when the firing of the fluticasone is coordinated with the exhalation of the patient.

Interventions

  • DEVICE Pressurized Metered-Dose Inhaler

Trial Details

FieldValue
Enrollment Target 34 participants
Start Date 2012-12
Est. Completion 2014-07
Philips Respironics

35 total trials

What the finished NCT01714063 record still lists

NCT01714063 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 34 participants, a relatively small participant target.

The record links to 0 conditions, and to 1 intervention - of which Pressurized Metered-Dose Inhaler is the first listed.

NCT01714063 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01714063 about?

NCT01714063 is a clinical study titled "Drug Delivery Via Pressurized Metered-dose Inhaler and Valved Holding Chamber in Asthmatic Children: Determination of Delivered Dose Following Coordinated and Uncoordinated Use". The primary objective of this study is to determine ex vivo the amount of fluticasone deposited onto a filter (delivered dose) interposed between the OptiChamber Diamond Valved Holding Chamber (VHC) mouthpiece and the subject's mouth during coordinated and uncoordinated actuation/inhalation maneuver...

What is the current status of trial NCT01714063?

This trial is currently completed. The enrollment target is 34 participants. The study started on 2012-12. Estimated completion is 2014-07.

What interventions are being tested in trial NCT01714063?

The interventions under investigation include: Pressurized Metered-Dose Inhaler (DEVICE).

Who is sponsoring clinical trial NCT01714063?

This trial is sponsored by Philips Respironics, which has 35 total clinical trials registered on ClinicalTrials.gov.

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Source: ClinicalTrials.gov NCT01714063, the US trial registry maintained by the National Library of Medicine. NCT01714063 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.