Clinical Trials Directory

Trials / Completed

CompletedNCT02198131

Pulsed Dye Laser in Treating Patients With Post Radiation Dysphonia

Pulsed Dye Laser for Treatment of Post Radiation Dysphonia

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
9 (actual)
Sponsor
Wake Forest University Health Sciences · Academic / Other
Sex
All
Age
Healthy volunteers
Not accepted

Summary

This pilot trial studies pulsed dye laser in treating patients with post radiation dysphonia. Dysphonia, or vocal cord scarring, can include trouble with the voice when trying to talk, such as hoarseness, change in voice pitch, and poor voice quality, and it commonly happens after radiation therapy for laryngeal cancer. Pulsed dye laser may improve post radiation dysphonia.

Detailed description

PRIMARY OBJECTIVES: I. To evaluate the use of pulsed dye laser in treatment of the dysphonia that commonly results after radiation therapy for laryngeal carcinoma. OUTLINE: Patients undergo pulsed dye laser monthly for three months. After completion of study treatment, patients are followed up at 1, 3, and 6 months.

Conditions

Interventions

TypeNameDescription
PROCEDURElaser therapyUndergo pulsed dye laser
OTHERquestionnaire administrationAncillary studies

Timeline

Start date
2009-10-01
Primary completion
2016-06-01
Completion
2016-06-01
First posted
2014-07-23
Last updated
2023-04-26

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT02198131. Inclusion in this directory is not an endorsement.