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CompletedNCT05689749SMIUpdated Jun 26, 2023

Superb Microvascular Imaging Ultrasonography of Lacrimal Gland in Patients With Sjögren Syndrome

An observational study in Inflammation, Sjogren's Syndrome and Gland; Inflammation, sponsored by Nigde Omer Halisdemir University. Completed at 1 site in Turkey. Open to participants aged 18 Years to 65 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2023-06-26.

Sponsored by Nigde Omer Halisdemir University · Observational

Study type
Observational
Model
Case-control
Time perspective
Prospective
Enrollment
42
Ages
18 Years to 65 Years
Sex
All
01

Study summary

A prospective study will be conducted to evaluate inflammatory activity in lacrimal glands due to Sjögren's syndrome on Superb Microvascular Imaging (SMI), gray scale ultrasound (US), color Doppler US and Power Doppler US.

Read the detailed description

In the disease activity index recommended by EULAR, the European Rheumatology Association, to evaluate the disease activity of patients with Sjögren's syndrome, it is recommended to measure the swelling in the gland by performing a clinical examination for glandular activity. However, it is not practical to measure the size of these glands due to their location.

In studies in which lacrimal glands were evaluated by ultrasonographic methods, parameters such as gland size measurement, gland heterogeneity and Doppler activity were reported to be very successful in differentiating patients from healthy controls.

Determining the presence and characteristics of vascular flow is an important part of ultrasonographic examinations. However, small vessels and low velocities are not always possible to detect with conventional color and power Doppler ultrasound. Sonographic examination will be inconclusive, especially if the presence of vascular flow or activity needs to be addressed as a basis for diagnosis and follow-up. Superb Microvascular Imaging (SMI) is a new vascular imaging mode that provides low speed and visualization of microvascular flow. SMI uses an algorithm that can suppress parasitic reverberations to extract flow signals and displays this information as a color overlay image or a monochromatic or color flow map.There are studies that report that Superb Microvascular Imaging (SMI), a new and up-to-date Ultrasonography technology, is more sensitive in detecting the activity of Rheumatic diseases. In this respect, there are no studies evaluating the inflammatory activity of lacrimal glands with SMI method.

Therefore, a prospective study will be conducted to evaluate the inflammation detecting performance of SMI, gray scale US, color Doppler US and Power Doppler US. The null hypothesis that there is no difference between Doppler US and SMI methods in the detection of increased inflammatory activity in Sjögren's syndrome patients.

02

Conditions studied

  • Inflammation
  • Sjogren's Syndrome
  • Gland; Inflammation

Keywords

  • superb microvascular imaging
  • microvascularization
  • Sjogren's syndrome
  • disease activitiy
03

In context

Sjogren's Syndrome

371 studies on the registry are indexed under Sjogren's Syndrome; 104 are open to participants now.

This study's enrollment of 42 is below the median of 114 across 113 observational studies indexed under Sjogren's Syndrome.

Browse Sjogren's Syndrome studies →

Lead sponsor

Nigde Omer Halisdemir University is the lead sponsor of 89 studies on the registry; 30 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

  • Patients who diagnosed as Sjögren's syndrome as the first group.
  • Healthy participants as the second group

Eligibility criteria

For the first group:

Inclusion Criteria:

  • Patients diagnosed with Sjögren's syndrome
  • Age between 18-65

Exclusion Criteria:

  • History of eye or face trauma or surgery
  • Diabetes mellitus
  • Pregnancy

For the second group:

Inclusion Criteria:

  • asymptomatic eye (no dry eye or dry mouth),
  • no previous trauma or surgery on face or eye,
  • no history of systemic inflammatory disorders.

Exclusion Criteria:

  • History of eye or face trauma or surgery
  • Diabetes mellitus
  • Pregnancy
  • Rheumatological diseases
05

Study design

Observational model
Case-control
Time perspective
Prospective
Enrollment
42 participants (actual)
Patient registry
No

Groups and cohorts

  • Participants with Sjögren's syndrome

    Participants with the diagnose of Sjögren's syndrome; Patients with a confirmed diagnosis who are being followed and treated by a rheumatologist.

    Device: Superb Microvascular Imaging (SMI) (Toshiba)

  • Volunteers who has not dry eye complaints and Sjögren's syndrome diagnosis.

    Voluntary participants without any rheumatic disease diagnosis, without Sjögren's syndrome diagnosis, without dry eye complaints will constitute the other group.

    Device: Superb Microvascular Imaging (SMI) (Toshiba)

Interventions

  • DeviceSuperb Microvascular Imaging (SMI) (Toshiba)

    To determine whether SMI has diagnostic value for detecting the inflammatory state in the lacrimal glands in Sjögren's syndrome and whether it has any superiority compared to Power Doppler and Color Doppler modalities.

06

What researchers measure

Primary outcomes

  1. Schirmer's test

    The tip of a special paper strip is placed inside the lower eyelid of each eye. During the test on both eyes, the eyes are asked to remain closed for 5 minutes. After 5 minutes the doctor removes the paper and measures how much is moistened.

    Time frame: 1 year

  2. Ocular Surface Disease Index (OSDI)

    Participants will be asked to answer a 12-question questionnaire asking about various conditions and symptoms related to dry eye.It is a 12-item questionnaire designed to provide a rapid assessment of the symptoms of ocular irritation consistent with dry eye disease and their impact on vision-related functioning. The 12 items of the OSDI questionnaire were graded on a scale of 0 to 4, where 0 indicates none of the time; 1, some of the time; 2, half of the time; 3, most of the time; and 4, all of the time. The total OSDI score was then calculated on the basis of the following formula: OSDI=\[(sum of scores for all questions answered) × 100\]/\[(total number of questions answered) × 4\].

    Time frame: 1 year

  3. McMonnies Dry Eye Questionnaire

    Participants will be asked to answer a 12-question questionnaire asking about various conditions and symptoms related to dry eye. It is presented on a single page and includes 12 questions that focus on clinical risk factors for DES. The questions employ polytomous response options that vary in number and type. For example, question 1 has three response categories consisting of yes (2), no (0), and uncertain (1), whereas question 9 has four response categories, consisting of never (0), sometimes (1), often (2), and constantly (3).

    Time frame: 1 year

  4. Ultrasonographic Evaluation; Superb Microvascular Imaging, GrayScale Imaging, Color Doppler Imaging, Power Doppler Imaging

    Four-stage classify will be use for grading these images; Grade 0: No vascularity in lacrimal and parotid gland, Grade 1: One or two focal color-encoded spots in lacrimal and parotid gland, Grade 2: One linear color-encoded line or more than two focal colorencoded spots in lacrimal and parotid gland, Grade 3: More than one linear color-encoded line in lacrimal and parotid gland

    Time frame: 1 year

07

Study locations

1 site
  • Nigde Omer Halisdemir University
    Niğde, 51700, Turkey
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 26, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT05689749
Lead sponsor
Nigde Omer Halisdemir University
Responsible party
Ender Salbaş (Physical Medicine & Rehabilitation Specialist, MD, Nigde Omer Halisdemir University) — Principal investigator
First posted
Jan 19, 2023
Start date
Apr 1, 2021
Primary completion
Jan 3, 2023
Completion
Jun 1, 2023
Last update
Jun 26, 2023

Study contacts

Ender Salbas, MD
study director · Nigde Omer Halisdemir University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Jun 2023. You cannot join it, but the record below documents what was studied.

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