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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02647931
Other study ID # 15-006933
Secondary ID
Status Completed
Phase N/A
First received November 13, 2015
Last updated March 12, 2018
Start date November 2015
Est. completion date March 2018

Study information

Verified date March 2018
Source Mayo Clinic
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Muscle tension dysphagia is a novel diagnostic taxonomy describing a subset of patient population with reported dysphagia who exhibit normal oropharyngeal and esophageal swallowing function as evidenced by videofluoroscopic swallow study. These patients also demonstrate abnormal supraglottic muscle tension during laryngoscopy as well as signs of laryngeal hypersensitivity and laryngopharyngeal reflux. Treatment of these patients with Proton Pump Inhibitor (PPI) therapy is a common practice however voice therapy invention targeting the unloading of the supraglottic muscle tension has been shown to be highly effective in symptom resolution per the investigators' clinical experience. The study is designed to answer efficacy of treatment being offered to patients with muscle tension dysphagia.


Recruitment information / eligibility

Status Completed
Enrollment 22
Est. completion date March 2018
Est. primary completion date March 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria

- Age 18-99

- Diagnosed with Muscle Tension Dysphagia

Exclusion Criteria

- Physical or emotional disorder preventing the completion of therapy

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Voice therapy for Muscle Tension Dysphagia
Voice therapy for Muscle Tension Dysphagia

Locations

Country Name City State
United States Mayo Clinic in Arizona Scottsdale Arizona

Sponsors (1)

Lead Sponsor Collaborator
Mayo Clinic

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Improvement of dysphagia measured via patient self-report measures Number of participants who report improvement of dysphagia symptoms following therapy. Duration of therapy, approximately 2 months