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NCT06174831 Clinical Trial

Study of a Series of Patients Treated for Retrograde Cricopharyngeal Muscle Dysfunction Syndrome

Deglutition Disorders Clinical Trial

— R-CPD-Syndrome  

Official title:
Study of a Series of Patients Treated for Retrograde Cricopharyngeal Muscle Dysfunction Syndrome

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT06174831
Other study ID # 8782
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date February 1, 2023
Est. completion date January 19, 2024

Study information
Verified date October 2023
Source University Hospital, Strasbourg, France
Contact Christian DEBRY, MD, PhD
Phone 33 3 88 12 76 44
Email christian.debry@chru-strasbourg.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

R-CPD syndrome (Retrograde Cricopharyngeal Dysfunction syndrome) is an inability to burp. It is a syndrome whose diagnosis is clinical, and for which there is effective treatment. Recently treated in the United States (first publication in 2019), this syndrome affects many patients in France and is currently unknown. This study concerns a series of patients treated at the University Hospitals of Strasbourg for a syndrome of retrograde dysfunction of the cricopharyngeus muscle having been treated by injection of botulinum toxin into the cricopharyngeus muscle.

Recruitment information / eligibility
Status Recruiting
Enrollment 30
Est. completion date January 19, 2024
Est. primary completion date January 2024
Accepts healthy volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Major subject (=18 years old) - Subject treated by injection of botulinum toxin into the cricopharyngeal muscle after having had a diagnosis of R-CPD in consultation between January 1, 2022 and December 31, 2022 - Subject not opposing the reuse of their data for the purposes of this research. Exclusion Criteria: - Subject having expressed opposition to participating in the study, - Subject under judicial protection - Subject under guardianship or curatorship

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
France Service d'ORL et de Chirurgie Cervico-faciale - CHU de Strasbourg - France Strasbourg

Sponsors (1)
Lead Sponsor Collaborator
University Hospital, Strasbourg, France

Country where clinical trial is conducted

France, 

Outcome
Type Measure Description Time frame Safety issue
Primary Retrospective description of the characteristics of a series of patients treated for dysphagia syndrome Retrospective study of medical files of patients treated in HUS between January 1, 2022 and December 31, 2022 Through study completion, an average of 2 months
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