Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

COMPLETED NA

Evaluation Of The Total Face Mask For Emergency Application In Acute Respiratory Failure

NCT00686257 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this study is to compare the Total Face Mask™ (Respironics, Inc., Pittsburgh, PA) (covering whole face) and the standard oronasal facemask (covering nose and mouth) for the emergency treatment of patients with acute respiratory failure with the machine blowing air into the mask placed on the face (noninvasive positive pressure ventilation) (NPPV).

Interventions

  • DEVICE Total face mask (interface for NPPV)
  • DEVICE Comfort full or RT040 oronasal mask (interface for NPPV)

Study Locations (2)

Massachusetts

  • Tufts Medical Center — Boston

Rhode Island

  • Rhode Island Hospital — Providence

Trial Details

FieldValue
Enrollment Target 60 participants
Start Date 2003-01
Est. Completion 2008-06
Phase NA

Sponsor

Tufts Medical Center

132 total trials

Interested in This Trial?

Always speak with your doctor before enrolling in a clinical trial.

Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00686257

The ClinicalTrials.gov registry entry for NCT00686257 describes a study currently listed as completed. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 60 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Tufts Medical Center, which has 132 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Acute Respiratory Insufficiency appearing as the primary indexed condition, and to 2 interventions — of which Total face mask (interface for NPPV) is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT00686257 reports 2 study locations spanning 2 distinct geographic areas — top geographies include Massachusetts, Rhode Island. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT00686257 about?

NCT00686257 is a clinical study titled "Evaluation Of The Total Face Mask For Emergency Application In Acute Respiratory Failure". The purpose of this study is to compare the Total Face Mask™ (Respironics, Inc., Pittsburgh, PA) (covering whole face) and the standard oronasal facemask (covering nose and mouth) for the emergency treatment of patients with acute respiratory failure with the machine blowing air into the mask placed...

What is the current status of trial NCT00686257?

This trial is currently completed. It is a NA study. The enrollment target is 60 participants. The study started on 2003-01. Estimated completion is 2008-06.

What conditions does trial NCT00686257 study?

This clinical trial studies the following conditions: Acute Respiratory Insufficiency. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT00686257?

The interventions under investigation include: Total face mask (interface for NPPV) (DEVICE), Comfort full or RT040 oronasal mask (interface for NPPV) (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT00686257?

This trial is sponsored by Tufts Medical Center, which has 132 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT00686257 being conducted?

This trial has 2 study locations across Massachusetts, Rhode Island. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial