Twitch Amplitude for Intubation

Age: 18+
Sex: Any
Trial Phase: Academic
Sponsor: Mayo Clinic
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

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.

Who Is on the Research Team?

JR

J. Ross Renew, MD

Principal Investigator

Mayo Clinic

Are You a Good Fit for This Trial?

This trial is for adults aged 18 or older who are willing to participate and can give informed consent. It is intended for people undergoing procedures that require intubation.

Inclusion Criteria

I am 18 years old or older.
I am willing to join the study and give my informed consent.

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

1-2 weeks

Treatment

Participants are intubated based on the T1/Tref ratio to determine intubating conditions

Baseline
1 visit (in-person)

Follow-up

Participants are monitored for intubating conditions and neuromuscular block levels

1 week

What Are the Treatments Tested in This Trial?

Trial Overview

The study tests different levels of muscle response (twitch amplitude ratios: <0.1, <0.3, <0.5) to find which provides the best conditions for safely inserting a breathing tube during anesthesia.

How Is the Trial Designed?

3

Treatment groups

Experimental Treatment

Group I: T1/Tref <0.5Experimental Treatment1 Intervention
Group II: T1/Tref <0.3Experimental Treatment1 Intervention
Group III: T1/Tref <0.1Experimental Treatment1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Mayo Clinic

Lead Sponsor

Trials
3,427
Recruited
3,221,000+