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
| Type | Name | Description |
|---|---|---|
| PROCEDURE | laser therapy | Undergo pulsed dye laser |
| OTHER | questionnaire administration | Ancillary 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.