Clinical Trials Directory

Trials / Terminated

TerminatedNCT04658342

Effects of Oral Cancer Treatments on Upper Esophageal Opening During Swallowing

Status
Terminated
Phase
Study type
Observational
Enrollment
5 (actual)
Sponsor
University of Wisconsin, Madison · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

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.

Conditions

Interventions

TypeNameDescription
DIAGNOSTIC_TESTVideofluoroscopic imaging (VFSS) with high-resolution manometry (HRM)The Videofluoroscopic Imaging (VFSS) is done by inserting a small catheter into the nose and down the throat. The catheter is approximately .4 millimeters in diameter. A trained speech-language pathologist will insert the catheter after applying numbing medicine, or topical anesthetic, inside the nose. The high-resolution manometry (HRM) is a swallowing pressure test done at the same time as the VFSS. The HRM will measure how strong the throat muscle squeeze the liquids and foods that a person swallows. The VFSS and HRM will occur about one month after surgery and three months after the completion of the radiation treatment.

Timeline

Start date
2021-04-16
Primary completion
2023-03-25
Completion
2023-03-25
First posted
2020-12-08
Last updated
2024-12-18

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT04658342. Inclusion in this directory is not an endorsement.