Natural History of Salivary Gland Dysfunction and Sjogren's Syndrome
Completed
Conditions studied: Lymphoma, Salivary Gland Disease, Sjogren's Syndrome, Xerostomia
In brief
This study will follow patients with salivary gland dysfunction to identify the long-term course of this disorder and its effects on the mouth, oral function, and overall health. Saliva is important in maintaining oral health and comfort. It moistens the mouth, lubricates food for easier swallowing, provides enzymes needed to begin the digestive process and promotes repair and cleansing of soft tissues of the mouth. Decreased salivary production or changes in salivary composition may affect oral and systemic health and cause an increase in tooth decay. Patients 4 years of age and older with dry mouth symptoms and a diagnosis of primary, secondary or incomplete Sj(SqrRoot)(Delta)gren s syndrome or salivary gland dysfunction due to radiation may be eligible for this study. Candidates will be screened with a complete medical and dental history and blood and saliva tests. Some patients will have a biopsy of the minor salivary glands, usually from the lower lip, to confirm or rule out the diagnosis of Sj(SqrRoot)(Delta)gren s syndrome and determine the extent of changes in the salivary glands. (A biopsy is the surgical removal of a small piece of tissue for laboratory examination.) The ability to taste and smell may also be evaluated, and patients may have an ultrasound examination of their swallowing function. Participants will have a general oral examination of the teeth and soft tissues of the mouth, general physical examination, eye examination and blood tests and will fill out a questionnaire on oral health and function. In addition, they will have the following tests and procedures: * Identification of possible fungal infection Patients rinse their mouth with 2 teaspoons of a salt-water solution and spit it in a sterile container for laboratory examination. If a fungal infection is detected, treatment will be offered. * Unstimulated salivary function assessment Saliva production is measured by collecting saliva samples through small suction cups connected to collection tubes over the salivary gland ducts in the mouth. * Stimulated salivary function assessment A sour-tasting liquid (2% citric acid) is applied to the top and sides of the tongue at 30-second intervals to stimulation saliva production while saliva is collected using the procedure described above. * Identification of markers of precancerous lesions The salivary gland biopsy done at the screening evaluation (or from outside sources) is examined for markers of precancerous lesions, as about 5 percent of patients with Sj(SqrRoot)(Delta)gren's syndrome develop a tumor called Non-Hodgkin s lymphoma. In some cases, the minor salivary glands may be re-biopsied a few years after the screening biopsy. Patients will be followed once a year with a comprehensive history and physical examination, eye examination, full oral examination, salivary function assessment and questionnaires about signs and symptoms of salivary gland dysfunction.
Key facts
- Study ID
- NCT00001852
- Run by
- National Institute of Dental and Craniofacial Research (NIDCR)
- People needed
- 560
- Starts
- 1999-04-09
- Expected to finish
- 2017-11-29
- Last updated by the study team
- 2019-12-17
Who can join
Age: 4 and older. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Age 18 years or older.
- Ability to give informed consent.
- EXCLUSION CRITERIA:
- History of bleeding diathesis or the current use of anticoagulants.
- Any uncontrolled or severe chronic disease.
You may not qualify if…
- Failure to complete evaluation procedures as specified in 84-D-0056.
- Diagnosis of drug-related xerostomia.
- Age less than 4 years.
- There are no exclusions based on gender, race, or ethnicity. Salivary gland dysfunction is uncommon in children and exceedingly rare in those less than 4 years old. Additionally, the evaluation method described in the protocol cannot be used in this age group.
- ULTRASOUND GUIDED CORE NEEDLE BIOPSY OF THE PAROTID GLAND
- Adult subjects already enrolled in this protocol and healthy volunteers will be eligible for this research procedure if they fulfill the criteria below and sign the parotid biopsy consent form. Healthy volunteers will be recruited only for the ultrasound guided core needle biospy of the parotid gland. They will sign the parotid biopsy consent form only.
- INCLUSION CRITERIA:
- Age 18 years or older.
- Ability to give informed consent.
- EXCLUSION CRITERIA:
- History of bleeding diathesis or the current use of anticoagulants.
- Any uncontrolled or severe chronic disease.
Where it is running
- National Institutes of Health Clinical Center, 9000 Rockville Pike — Bethesda, Maryland, United States
Full record on ClinicalTrials.gov
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