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Voice and Swallow Outcomes After Office-based Injection Laryngoplasty in Patients With Glottal Insufficiency

NCT06161064 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 10

Last updated 2023-12-07

No results posted yet for this study

Summary

The purpose of this study is to evaluate voice quality and swallow outcomes of office-based injection laryngoplasty using hyaluronic acid in patients with Glottal insufficiency and assess all cases after 1, 3 and 6 months.

Conditions

  • Voice and Swallow Outcomes After Injection Laryngoplasty in Patients With Glottal Insufficiency

Interventions

DRUG

Hyaluronic acid

hyaluronic acid is temporary material using for augmentation of vocal folds in patients with glottal insufficiency

Sponsors & Collaborators

  • Sohag University

    lead OTHER

Principal Investigators

  • ayaa bakhet · Sohag University

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

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

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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 NCT06161064 on ClinicalTrials.gov