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NCT05989880 · ClinicalTrials.gov registry record · NA

Pilot Feasibility Trial of the SafeLM Supraglottic Airway (SGA)

A NA study of Anesthesia, sponsored by The University of Texas Health Science Center, Houston.

Recruiting
Registry status
NA
Development phase
60
Enrollment target
1
Study location

NCT05989880 is a NA study of Anesthesia that is actively recruiting participants, run by The University of Texas Health Science Center, Houston. The registered enrollment target is 60 participants, below the 109,409-participant average among 57 other Anesthesia trials with a reported enrollment target (100% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT05989880, a NA study of Anesthesia, is actively recruiting participants, sponsored by The University of Texas Health Science Center, Houston.

RECRUITING
Registry status
NA
Development phase
60 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to assess the feasibility of SafeLM as a primary airway device and as a conduit for intubation with and without the use of a bougie

Conditions Studied

Interventions

  • DEVICE SafeLM as a supraglottic airway device with video capability
  • DEVICE SafeLM as a supraglottic airway device without video capability
  • DEVICE SafeLM as a conduit for intubation using an endotracheal tube with video capability
  • DEVICE SafeLM as a conduit for intubation using a bougie with video capability

Study Locations (1)

Texas

  • The University of Texas Health Science Center at Houston - Houston

Trial Details

FieldValue
Enrollment Target 60 participants
Start Date 2023-09-19
Est. Completion 2025-12-02
Phase NA

What the Registry Record Tells You About NCT05989880

The ClinicalTrials.gov registry entry for NCT05989880 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 60 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 109,409-participant average among 57 other Anesthesia trials with a reported enrollment target (100% lower). The listed sponsor is The University of Texas Health Science Center, Houston, which has 732 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Anesthesia appearing as the primary indexed condition, and to 4 interventions - of which SafeLM as a supraglottic airway device with video capability is the first listed.

NCT05989880 reports 1 study location spanning 1 distinct geographic area - top geographies include Texas.

Frequently Asked Questions

What is clinical trial NCT05989880 about?

NCT05989880 is a clinical study titled "Pilot Feasibility Trial of the SafeLM Supraglottic Airway (SGA)". The purpose of this study is to assess the feasibility of SafeLM as a primary airway device and as a conduit for intubation with and without the use of a bougie

What is the current status of trial NCT05989880?

This trial is currently recruiting. It is a NA study. The enrollment target is 60 participants. The study started on 2023-09-19. Estimated completion is 2025-12-02.

What conditions does trial NCT05989880 study?

This clinical trial studies the following conditions: Anesthesia.

What interventions are being tested in trial NCT05989880?

The interventions under investigation include: SafeLM as a supraglottic airway device with video capability (DEVICE), SafeLM as a supraglottic airway device without video capability (DEVICE), SafeLM as a conduit for intubation using an endotracheal tube with video capability (DEVICE), SafeLM as a conduit for intubation using a bougie with video capability (DEVICE).

Who is sponsoring clinical trial NCT05989880?

This trial is sponsored by The University of Texas Health Science Center, Houston, which has 732 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05989880 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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