Vitamin A Status in Patients With Vocal Fold Leukoplakia

University of Wisconsin (UW)

Status: Invitation-only

Conditions: Leukoplakia; Vitamin A Deficiency; Vocal Cord Neoplasm; Vitamin A

Study type: Observational

Funder types: Other; NIH

Identifiers

NCT05323292

07/01/2021 (Other Identifier)

2021-1045 (Other Identifier)

R01DC019357 (U.S. NIH Grant/Contract)

SMPH/SURGERY/SURGERY*OT (Other Identifier)

A539770 (Other Identifier)

Details and patient eligibility

About

This study will determine systemic vitamin A status and lesion histopathology of participants with vocal fold hyperkeratosis resulting in clinical leukoplakia.

Full description

The investigator's overarching goal is to determine if there is a pathophysiologic rationale for vitamin A supplementation in the treatment of vocal fold hyperkeratosis. Vocal fold hyperkeratosis is an accumulation of epithelial surface keratin resulting in clinical leukoplakia. It is primarily managed using destructive techniques that risk iatrogenic injury, fibrosis, and voice impairment. Given the potential morbidity of biopsy and lesion removal, there is a need for new approaches to the prevention and treatment of vocal fold leukoplakic disorders that are non-destructive. Vitamin A is a key regulator of epithelial health and systemic vitamin A deficiency could directly contribute to hyperkeratosis. Based on vitamin A's importance to vocal fold stellate and epithelial cell biology and its direct relevance to vocal fold hyperkeratosis, this study will assess vitamin A status in participants with vocal fold hyperkeratosis. An association would suggest further study on the effects of vitamin A optimization and/or supplementation in patients with leukoplakia, as well as an adjuvant therapy in participants for whom surgical treatment is indicated.

Enrollment: 90 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Willing to provide informed consent.

2. Willing to comply with all study procedures and be available for the duration of the study.

3. Ability to take oral medication.

4. At least 18 years of age.

5. Leukoplakia study groups:

   1. Leukoplakia due to hyperkeratosis with dysplasia: biopsy-confirmed diagnosis of hyperkeratosis with dysplasia.
   2. Leukoplakia due to hyperkeratosis with no dysplasia: biopsy-confirmed diagnosis of hyperkeratosis with no dysplasia.

6. Control group: Laryngoscopy showing no evidence of vocal fold epithelial disease.

Exclusion criteria

1. History of malignant vocal fold epithelial pathology.
2. History of metabolic or liver disorder.
3. History of anorexia or bulimia.
4. Pregnant, lactating, or planning on becoming pregnant during the study period.
5. History of >4.5 kg weight loss in the past 90 days.
6. Medical or other inability to complete an 8 hour fast.
7. Acute respiratory or gastrointestinal illness.
8. Currently incarcerated.
9. Impaired decision-making capacity.
10. No or limited English speaking ability; illiterate or low-literacy ability.
11. Profound visual or hearing impairment that limits written or verbal communication.
12. Status relationship with a member of the study team.
13. Not suitable for study participation due to other reasons at the discretion of the investigators.

Trial design

90 participants in 3 patient groups

Leukoplakia due to hyperkeratosis with dysplasia

Description:

Biopsy-confirmed diagnosis of hyperkeratosis with dysplasia.

Leukoplakia due to hyperkeratosis with no dysplasia

Description:

Biopsy-confirmed diagnosis of hyperkeratosis with no dysplasia.

Control group

Description:

Laryngoscopy showing no evidence of vocal fold epithelial disease.