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Effects of Oral Cancer Treatments on Upper Esophageal Opening During Swallowing

University of Wisconsin (UW) logo

University of Wisconsin (UW)

Status

Terminated

Conditions

Cancer of Head and Neck

Treatments

Diagnostic Test: Videofluoroscopic imaging (VFSS) with high-resolution manometry (HRM)

Study type

Observational

Funder types

Other

Identifiers

NCT04658342
2020-0495 (Other Identifier)
Protocol Version 4/26/2022 (Other Identifier)
UW20051 (Other Identifier)
A539770 (Other Identifier)
SMPH/SURGERY/OTOLARYNGOLOGY (Other Identifier)

Details and patient eligibility

About

The purpose of this study is to investigate post-operative and post-radiation upper esophageal sphincter opening measures in oral cancer patients, compare measures to age- and gender-matched healthy adults, and determine relationships with patient swallowing outcomes and quality of life.

Enrollment

5 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Oral cancer that includes tongue or floor of mouth clinical stage T1 or higher
  • May have disease that extends to base of tongue or other site as long as floor of mouth or tongue are involved
  • Adults at least 18 years of age

Exclusion criteria

  • Oral cancer of the lip, cheek, palate or other site not impacting tongue or floor of mouth musculature
  • History of floor of mouth, tongue base, pharyngeal or laryngeal surgical resection
  • History of radiation treatment to the head and neck
  • History of dysphagia prior to onset of oral cancer symptoms
  • Allergy to lidocaine, barium, adhesive tape or apple flavoring
  • Woman of childbearing years who are pregnant

Trial design

5 participants in 1 patient group

Oral Cancer Patients
Treatment:
Diagnostic Test: Videofluoroscopic imaging (VFSS) with high-resolution manometry (HRM)

Trial contacts and locations

1

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Central trial contact

Molly Knigge, MS, CCC-SLP; Mary Lynch

Data sourced from clinicaltrials.gov

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