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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03143413
Other study ID # CHU-323
Secondary ID 2016-A01256-45
Status Recruiting
Phase
First received
Last updated
Start date March 24, 2017
Est. completion date May 2019

Study information

Verified date April 2018
Source University Hospital, Clermont-Ferrand
Contact Patrick LACARIN
Phone 04 73 75 11 95
Email placarin@chu-clermontferrand.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Systemic sclerosis is an autoimmune connective tissue disease with undefined etiology and characterized by progressive fibrosis of the skin and major organs. Dry eyes and / or buccal syndrome is commonly reported in patients with systemic sclerosis. Goujerot-Sjogren syndrome is a chronic autoimmune disorder that is characterized by dryness of the eyes (xerophthalmia) and / or mouth (xerostomia). It may be primary or secondary to another connective tissue disease (such as lupus, rheumatoid arthritis or other). Several criteria have been validated to classify the SS but require a labial salivary gland biopsy, invasive act which complications can sometimes be reported (hematoma, lip sensory defect).

Several scores based on the evaluation of the ultrasound homogeneity of the salivary glands were developed but no studies have evaluated ultrasound abnormalities of salivary glands in patients with systemic sclerosis.


Description:

Descriptive explorative study of three population showing sicca symptoms (Systemic sclerosis, Gougerot-Sjogren syndrome, Sicca-Asthenia-Polyalgia syndrome).

Patient will be enrolled in the rheumatology department of University hospital of Clermont-Ferrand (France).

Salivary glands ultrasonography will be performed on all patients enrolled by the same expert and blinded to the diagnosis of the patient. Echostructure of the two salivary glands will be graded 0 to 4 and the size calculated.


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date May 2019
Est. primary completion date March 2019
Accepts healthy volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Systemic sclerosis diagnosis established by a rheumatologist and met ACR 2012 criteria

- Or primary Gougerot-Sjogren patient who met American-European Consensus Group (AECG) classification criteria.

- Or patient presenting a sicca syndrome but not met Gougerot-Sjogren criteria

Exclusion Criteria:

- History of radiotherapy on face and neck

- Infection such as VIH or Hepatitis C

- Sarcoidosis

- Amylosis

- Wearing contact lenses

- Hyper IgG4 syndrome

Study Design


Intervention

Other:
Ultrasonography
Patient will be enrolled in the rheumatology department of University hospital of Clermont-Ferrand (France). Salivary glands ultrasonography will be performed on all patients enrolled by the same expert and blinded to the diagnosis of the patient. Echostructure of the two salivary glands will be graded 0 to 4 and the size calculated.

Locations

Country Name City State
France CHU Clermont-Ferrand Clermont-Ferrand Auvergne

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Clermont-Ferrand

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Jousse-Joulin ultrasonography score Echostructure of the two salivary glands will be graded 0 to 4 and the size calculated. the day of inclusion
Secondary Ultrasonography score equal or higher than 2 on at least one salivary gland the day of inclusion
Secondary Ultrasonography score equal or higher than 3 on at least one salivary gland the day of inclusion
Secondary Global ultrasonography score higher than 6/16 the day of inclusion
Secondary Salivary glands area the day of inclusion
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