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A Study Of T1/Tref Intubating Conditions

NCT07483164 · Status: ENROLLING_BY_INVITATION · Phase: NA · Type: INTERVENTIONAL · Enrollment: 108

Last updated 2026-05-19

No results posted yet for this study

Summary

The purpose of this study is to determine the maximum ratio of the twitch amplitude (T1) to the reference twitch (Tref) amplitude (T1/Tref) that provides excellent intubating conditions.

Conditions

  • Intubation

Interventions

DEVICE

Twitch amplitude <0.1

(T1/Tref) \<0.1

OTHER

Twitch amplitude <0.3

(T1/Tref) \<0.3

OTHER

Twitch amplitude <0.5

(T1/Tref) \<0.5

Sponsors & Collaborators

Principal Investigators

  • J. Ross Renew, MD · Mayo Clinic

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-05-31
Primary Completion
2026-12-31
Completion
2026-12-31
FDA Device
Yes

Countries

  • United States

Study Locations

More Related Trials

Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07483164 on ClinicalTrials.gov