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Voice Rest and Injection Laryngoplasty

NCT05542550 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 150

Last updated 2024-01-19

No results posted yet for this study

Summary

The purpose of this study is to evaluate the subjective, objective, and aerodynamic impact of voice rest following injection augmentation and compare the outcomes to patients with no post-procedure voice restrictions.

Conditions

  • Vocal Cord Paralysis

Interventions

BEHAVIORAL

Voice Rest

Voice rest restricting patient phonation

BEHAVIORAL

No Voice Rest

No Voice rest

Sponsors & Collaborators

  • University of Colorado, Denver

    collaborator OTHER

  • University of Virginia

    lead OTHER

Principal Investigators

  • James J Daniero, MD · University of Virginia

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
89 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-08-01
Primary Completion
2024-12-31
Completion
2024-12-31

Countries

  • United States

Study Locations

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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 NCT05542550 on ClinicalTrials.gov