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No Post Intubation Laryngeal Symptoms

NCT05383417 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 100

Last updated 2025-09-10

Study results available
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Summary

The purpose of the study is to test a novel endotracheal tube support device that reduces pressure of the tube on the voice box for prevention of post intubation laryngeal symptoms including sore throat, change in voice and trouble swallowing.

Conditions

  • Sore-throat
  • Dysphonia
  • Dysphagia
  • Intubation Complication
  • Anesthesia Intubation Complication
  • Anesthesia Morbidity
  • Anesthesia Complication
  • Anesthesia; Adverse Effect
  • Anesthesia; Reaction
  • Throat Disorder
  • Throat; Wound
  • Throat Injury

Interventions

DEVICE

EndoClip

Clip attached to mid portion of the endotracheal tube.

Sponsors & Collaborators

Principal Investigators

  • Andrew Vahabzadeh-Hagh, MD · UC San Diego Health

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-11-08
Primary Completion
2023-09-21
Completion
2023-09-21
FDA Device
Yes

Countries

  • United States

Study Locations

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Entities

Diseases
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 NCT05383417 on ClinicalTrials.gov