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NCT02198131 · ClinicalTrials.gov registry record · NA
Pulsed Dye Laser in Treating Patients With Post Radiation Dysphonia
A NA study of Oral Complications of Radiation Therapy and Stage I Laryngeal Cancer, sponsored by Wake Forest University Health Sciences.
- Completed
- Registry status
- NA
- Development phase
- 9
- Enrollment target
- 1
- Study location
NCT02198131 is a NA study of Oral Complications of Radiation Therapy and Stage I Laryngeal Cancer that has completed, run by Wake Forest University Health Sciences. The registered enrollment target is 9 participants. The trial reports 1 study location across 1 state.
The verdict
NCT02198131, a NA study of Oral Complications of Radiation Therapy and Stage I Laryngeal Cancer, has completed, sponsored by Wake Forest University Health Sciences.
- COMPLETED
- Registry status
- NA
- Development phase
- 9 participants
- Enrollment target
- 1
- Study location
Study 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.
Conditions Studied
Interventions
- OTHER questionnaire administration
- PROCEDURE laser therapy
Study Locations (1)
North Carolina
- Comprehensive Cancer Center of Wake Forest University - Winston-Salem
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 9 participants |
| Start Date | 2009-10 |
| Est. Completion | 2016-06 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02198131
The ClinicalTrials.gov registry entry for NCT02198131 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 9 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Wake Forest University Health Sciences, which has 1,140 total studies on file at ClinicalTrials.gov.
The record links to 3 conditions, with Oral Complications of Radiation Therapy appearing as the primary indexed condition, and to 2 interventions - of which questionnaire administration is the first listed.
NCT02198131 reports 1 study location spanning 1 distinct geographic area - top geographies include North Carolina.
Frequently Asked Questions
What is clinical trial NCT02198131 about?
NCT02198131 is a clinical study titled "Pulsed Dye Laser in Treating Patients With Post Radiation Dysphonia". 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 ...
What is the current status of trial NCT02198131?
This trial is currently completed. It is a NA study. The enrollment target is 9 participants. The study started on 2009-10. Estimated completion is 2016-06.
What conditions does trial NCT02198131 study?
This clinical trial studies the following conditions: Oral Complications of Radiation Therapy, Stage I Laryngeal Cancer, Stage II Laryngeal Cancer.
What interventions are being tested in trial NCT02198131?
The interventions under investigation include: questionnaire administration (OTHER), laser therapy (PROCEDURE).
Who is sponsoring clinical trial NCT02198131?
This trial is sponsored by Wake Forest University Health Sciences, which has 1,140 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT02198131 being conducted?
This trial has 1 study location across North Carolina. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Oral Complications of Radiation Therapy
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