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COMPLETED NA

Assessment of an Oral Endotracheal Subglottic Tube Holder

NCT03328182 · View on ClinicalTrials.gov ↗

Study Summary

This study is designed to assess the acceptability and usability of a new Endotracheal Tube (ET) holding device for an orally intubated patient.

Conditions Studied

Interventions

  • DEVICE New oral endotracheal tube holder

Study Locations (4)

Oregon

  • Legacy Mount Hood Medical Center — Gresham
  • Legacy Good Samaritan Medical Center — Portland
  • Legacy Emanuel Hospital & Health Center — Portland

California

  • Community Regional Medical Center — Fresno

Trial Details

FieldValue
Enrollment Target 34 participants
Start Date 2017-10-23
Est. Completion 2018-06-15
Phase NA

Sponsor

Hollister Incorporated

3 total trials

Interested in This Trial?

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT03328182

The ClinicalTrials.gov registry entry for NCT03328182 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 34 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Hollister Incorporated, which has 3 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 Intubation appearing as the primary indexed condition, and to 1 intervention — of which New oral endotracheal tube holder 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: NCT03328182 reports 4 study locations spanning 2 distinct geographic areas — top geographies include Oregon, California. 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 NCT03328182 about?

NCT03328182 is a clinical study titled "Assessment of an Oral Endotracheal Subglottic Tube Holder". This study is designed to assess the acceptability and usability of a new Endotracheal Tube (ET) holding device for an orally intubated patient.

What is the current status of trial NCT03328182?

This trial is currently completed. It is a NA study. The enrollment target is 34 participants. The study started on 2017-10-23. Estimated completion is 2018-06-15.

What conditions does trial NCT03328182 study?

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

What interventions are being tested in trial NCT03328182?

The interventions under investigation include: New oral endotracheal tube holder (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT03328182?

This trial is sponsored by Hollister Incorporated, which has 3 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT03328182 being conducted?

This trial has 4 study locations across California, Oregon. 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