Oral Health, Saliva Viscosity and Composition in Oculo-Pharyngeal Muscular Dystrophy (OPMD)

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorSheba Medical Center

About this trial

The goal of this observational study is to explore whether oral health and saliva viscosity and composition in Oculopharyngeal Muscular Dystrophy (OPMD) is different from control subjects.

The main questions it aims to answer are:

Do swallowing disturbances in OPMD adversely affect oral health? Is saliva thickness (viscosity) is increased in OPMD? Does saliva in OPMD contains biochemical markers of the disease?

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients with OPMD and their spouses or household members

Disqualifiers

• Pregnancy or presence of any disease that may affect a composition of saliva

Trial population

The Patients group: consisted OPMD patients enrolled in IsrOPMD registry at the multidisciplinary OPMD service at the Sheba Medical Center. The Control group: patients' spouse or household member without OPMD.

Trial design

Design model

Family-based

Time perspective

Cross-sectional

Treatments tested in this trial

Not listed

Trial groups

100 Participants
are grouped into 2 trial groups
Group A: Patients
Group B: Control

Trial outcomes

Primary outcomes

1

Saliva Viscosity

Viscosity of unstimulated whole saliva

Time frame
Upon enrollment in the study

Secondary outcomes

1

Oral health indices

DMFT, presence of tongue coating, clinical appearance of saliva and saliva-related complains

Time frame
Upon enrollment in the study

Other outcomes

1

Concentration of Metabolites in saliva

Differences in concentration of metabolites in unstimulated whole saliva of patients and control groups.

Time frame
Upon enrollment in the study

Sponsors and contacts

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