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Laser Treatment Of Vascular Lesions On Vocal Cords

Laser Atraumatic Treatment Of Ectasias On Vocal Cords

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00592644
Enrollment
7
Registered
2008-01-14
Start date
2005-03-31
Completion date
2008-10-31
Last updated
2011-03-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Ectasia

Keywords

ectasia, vascular lesions, vocal cords, voice, pulsed dye laser

Brief summary

Small vascular malformations (SVM) on the vocal fold is a common problem that can disturb the voice. The pulsed dye laser (PDL) has been successfully used for treatment of blood vessel abnormalities in surface tissue, through its high selectivity for destroying targeted blood vessels while sparing normal tissue. However, there is no study to determine its clinical benefit for treatment of SVMs on vocal fords. In this proposed study, we plan to make such a determination.We will determine whether PDL will produce better and quicker voice improvement than the conventional surgeries, in 20 patients (10 cases of each group) with vocal fold SVM. We expect that this less invasive laser treatment will provide an ideal and excellent option for this disease.

Detailed description

Clinically, small vascular malformations (SVM) on the vocal fold is a common problem that can disturb the voice. Currently, this problem is treated with endoscopic microsurgery with the use of a Carbon dioxide (CO2) laser or other microsurgeries. However, those treatments are unsatisfactory because of their invasive nature. The pulsed dye laser (PDL) has been successfully used for treatment of blood vessel abnormalities in surface tissue, through its high selectivity for destroying targeted blood vessels while sparing normal tissue. Even thought this process has been in use clinically for the past 5 years, there is no study to determine its clinical benefit for treatment of SVMs on vocal fords, by comparing it with routine surgeries. In this proposed study, we plan to make such a determination, by comparing the voice recovery and voice improvement between this laser and those routine surgeries (with CO2 laser or cold instrument). Our specific aim is to determine whether PDL will produce better and quicker voice improvement than the conventional surgeries, in 20 patients (10 cases of each group) with vocal fold SVM. This is the first study to determine clinical benefit of the microvascular targeting (MVT) technique of laser to treat vocal fold SVMs, by a comparison of the voice results between these two groups. We expect that this less invasive laser treatment will provide an ideal and excellent alternative to current surgical approaches for treatment of this disease.

Interventions

PROCEDUREPulse Dye laser (PDL)

one-time PDL, in 10 subjects

PROCEDURECO2 laser or other traditional surgeries

once-time CO2 laser or other conventional surgeries, in other 10 subjects

Sponsors

National Institute on Deafness and Other Communication Disorders (NIDCD)
CollaboratorNIH
Boston University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 64 Years
Healthy volunteers
No

Inclusion criteria

1. have SVMs or other small (2.0 mm diameter or less) vasculature-related lesions on vocal fold 2. Hoarseness or other symptoms of alteration in phonation is persistent least for 3 months 3. have (or have a high risk of) recurrent vocal fold hemorrhage, SVM enlargement or persistent fold vibratory abnormality 4. 18 years of age or older 5. Failure to response to voice training or other non-surgical treatments 6. Require CO2 laser ablation or other surgical removal of the lesion 7. Willingness to participate in a 6-month study and adhere to the follow-up schedule 8. A signed informed consent form

Exclusion criteria

1. Age less than 18 years, or older than 64 2. Any evidence of mental impairment such that the patient cannot understand the protocol or be in a position to sign the informed consent form 3. Clinical or histological evidence of malignant conversion 4. Lesion to be larger than 2.00 mm diameter or those non-vascular lesions 5. Pregnant women 6. Severity of disease such that airway patency is in immediate danger 7. Patients for whom the voice quality is particularly important: including signers, actors, or other similar professions or person who requires a very high voice quality

Design outcomes

Primary

MeasureTime frame
Recovery of Voice5 months

Secondary

MeasureTime frame
clearance of lesion5 months

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026