Rigshospitalet
Copenhagen, 2100, Denmark
Location status: Recruiting
Location contact
Joachim Hansen, M.D PhD-fellow
CONTACT
Joachim Hansen, M.D PhD-fellow
PRINCIPAL_INVESTIGATOR
NCT Number: NCT06805448
Living with dry mouth significantly impacts daily life, causing constant discomfort. It makes it harder to talk, eat solid food (increasing the risk of malnutrition), swallow, and sleep well. It also raises the risk of tooth decay. One common cause of dry mouth is Sjögren's Syndrome.
Sjögren's Syndrome is a common chronic autoimmune disease. In this disease, the immune system attacks the body's own saliva glands, reducing saliva production and leading to severe dry mouth and its associated symptoms.
Current treatments for dry mouth are temporary and only last a short time (from a few minutes to a few hours). Therefore, new treatment options are needed.
Research has shown that mesenchymal stem cells can be used to treat dry mouth with promising results. These stem cells can be injected into a vein or directly into the saliva glands. Although the exact mechanism is not fully understood, studies suggest that stem cells can positively affect the immune system, reduce inflammation, regenerate tissue, and reverse scarring.
This research group has been studying stem cell treatment for dry mouth for over 10 years and is internationally recognized. The group have conducted three studies where we injected stem cells into the saliva glands of patients with dry mouth due to radiation therapy for head or neck cancer. Results showed a 30%-50% increase in saliva production and a significant reduction in dry mouth symptoms. No studies have yet investigated injecting stem cells into the saliva glands of patients with dry mouth due to Sjögren's Syndrome. One study did inject stem cells into tear glands with promising results. Therefore, this study aim to investigate injecting stem cells into the saliva glands of patients with dry mouth due to Sjögren's Syndrome.
For this study, mesenchymal stem cells harvested from the fat tissue of healthy adult donors is used. This type of stem cell is better at reversing scarring and forming new blood vessels. The procedure is quick and has few side effects, and donors benefit from the fat removal. The fat is typically taken from the abdominal area. Donors are tested for various diseases to ensure they are healthy. Previous studies have shown that the treatment is safe with only a few temporary side effects.
The hypothesis is that injecting stem cells into the saliva glands of patients with dry mouth due to Sjögren's Syndrome will improve saliva production and reduce dry mouth symptoms. The study aims to determine if this treatment increases saliva production and reduces symptoms caused by dry mouth.
To test these hypotheses, the study will include:
1. The treatment itself with either stem cells or a placebo (sterile saline). 2. Multiple saliva tests to measure saliva production. 3. Saliva samples stored for later analysis to see if the saliva's ability to protect teeth and aid digestion changes after stem cell treatment. 4. A blood test to examine the immune system's response to the stem cell treatment. 5. A clinical examination to see if the stem cell treatment affects Sjögren's Syndrome symptoms elsewhere in the body. 6. Questionnaires to assess participants' perceptions of changes in dry mouth symptoms after treatment.
The treatment involves injecting either stem cells or a placebo into the two saliva glands near the jaw, guided by an ultrasound scan. The procedure takes 10 minutes.
Although stem cell treatment has been shown to be safe, safety will be monitored in this study. At all three visits, participants will be asked about any side effects, which will be categorized as serious or mild, and as treatment-related or not. Follow-up and treatment plans will be made for any side effects. Participants will also always have direct access to the treating doctor.
The study will be monitored by the Danish Medicines Agency and the GCP unit, which ensures that all rules and laws are followed.
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Phase 1 / Phase 2
Copenhagen, 2100, Denmark
Location status: Recruiting
Joachim Hansen, M.D PhD-fellow
CONTACT
Joachim Hansen, M.D PhD-fellow
PRINCIPAL_INVESTIGATOR
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Allogeneic adipose-derived mesenchymal stromal / stem cells in 10% DMSO
Isotonic sterile saline water
Time frame: From baseline to 4 months after treatment
Time frame: From baseline to 4 and 12 months after treatment
Time frame: From baseline to 4 and 12 months after treatment
Time frame: From baseline to 4 and 12 months after treatment
The concentrations of the specific electrolyte, total protein and IgA will be compared to reference values.
Time frame: From baseline to 4 and 12 months after treatment
Serum will be frozen until the end of the trial and all samples will be analyzed together. The blood samples will be analyzed for HLA class I and class II antibodies with the Luminex platform (Luminex 200 system or LABScan3D) and will be reported as HLA antibodies present/not present in the samples.
Time frame: From baseline to 4 and 12 months after treatment
Time frame: From baseline to 4 and 12 months after treatment
Measured as changes in the OMERACT US system
Time frame: From baseline to 4 and 12 months after treatment
Time frame: From baseline to 4 and 12 months after treatment
Time frame: From baseline to 4 and 12 months after treatment
This PROM will be compared by converting to summary-scores ranging from 0-100.
Time frame: From baseline to 4 and 12 months after treatment
This outcome will be compared by converting to summary-scores ranging from 0-100
Time frame: From baseline to 4 and 12 months after treatment
This outcome will be compared by converting to summary-scores ranging from 0-100
Contact information is provided by the study sponsor or research team.
Rigshospitalet, Denmark
Other
Intraglandular Treatment With Adipose-derived Mesenchymal Stem Cells in Patients With Xerostomia Due to Sjögrens Disease
Acronym: ASSIX
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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