NCT06987565RecruitingPhase 2
Transcutaneous Vagus Nerve Stimulation in SLE
Transcutaneous Vagus Nerve Stimulation in SLE (TvSSLE)
Source: ClinicalTrials.gov · Last updated 17 Sept 2026
Brief summary (registry, in English)
Systemic lupus erythematosus (SLE) is a chronic autoimmune inflammatory disease. Joint and muscle pain and fatigue are extremely common among patients and contribute to a reduced quality of life. Available therapies may be associated with significant side effects and many patients do not achieve an adequate response to these treatments. Therefore, there is an unmet need to develop new strategies to reduce pain and fatigue. Filling this need would significantly improve patients' quality of life. This trial will evaluate the effects of a novel approach, stimulating the vagus nerve, a nerve originating in the brain as a potential therapeutic intervention for treatment of musculoskeletal pain and fatigue. Vagus nerve stimulation has multiple beneficial effects and is one of the body's own ways to modulate the immune system. One can stimulate the vagus nerve via the skin at the neck or at specific locations in the ear, (transcutaneous vagus nerve stimulation: tcVNS). We recently completed a short, small scale randomized, placebo controlled trial of tcVNS in patients with SLE and observed dramatic benefits on musculoskeletal pain and fatigue. The treatment was safe without side effects. We are therefore proposing a longer trial to validate our initial findings and to look at durability. In this study, 18 patients with musculoskeletal pain will be followed for 2 months and will receive tcVNS or placebo (sham stimulation) for 5 minutes/day for 28 days. Patients will have a 1 out of 3 chance of receiving sham stimulation and neither the patient nor the evaluating investigator will know the actual treatment. The stimulations are self-administered, are non-painful and have not been associated with serious risks. After 28 days of stimulation, treatment will be discontinued and patients will be monitored for an additional 28 days to evaluate durability. Pain, fatigue and disease activity will be evaluated as well as possible side effects will be monitored throughout the trial. This study will also explore biologic mechanisms that may be responsible for the potential clinical effects. This will include possible effects of stimulation on gut permeability and the stool microbiome, areas that may play a significant role contributing to SLE disease and its manifestations. The development of an effective treatment without significant side effects would be extremely valuable and a significant advance for patients with SLE. If efficacious, tcVNS offers a non-toxic, non-immunosuppressive strategy to control two of the most common symptoms of this disease.
- Status (registry)
- Recruiting
- Phase (registry)
- Phase 2
- Study type
- Interventional
- Enrollment
- 18 (estimated)
- First submitted
- 23 Apr 2025
- Start date
- 25 Jul 2025
- Primary completion date
- Feb 2027
- Lead sponsor
- Northwell Health
- Diseases
- Lupus (SLE)
- NCT number
- NCT06987565
What you commit to
- Study type: Interventional · Phase 2
- Planned participants: 18
- From 25 Jul 2025 to the primary completion date, Feb 2027
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Treatment with cyclophosphamide within 2 months of baseline,
- Expectation to increase steroids and/or immunosuppressive treatment,
- Treatment with an anti-cholinergic medication, including over the counter medications,
- Any implantable electronic devices including pacemakers, defibrillators, hearing aids, cochlear implants or deep brain stimulators,
- Joint replacement within 60 days prior to study enrollment or planned within the course of the study,
- Any planned surgical procedure requiring general anesthesia within the course of the study,
- Investigational drug and/or treatment during the 28 days or seven half-lives of the investigational drug prior to the start of study drug dosing (Day 0), whichever is the greater length of time,
- Comorbid disease that has previously required administration of corticosteroid use,
- Chronic treatment with narcotic medication,
- Prior receipt of transauricular vagus nerve stimulation in a clinical trial,
Other illness
- Anti-phospholipid syndrome,
- Chronic inflammatory disorders apart from SLE affecting the joints,
- Active infection including hepatitis B or hepatitis C at baseline,
- Any condition which, in the opinion of the investigator, would jeopardize the subject's safety following exposure to a study intervention,
- Known allergy to mannitol or lactulose,
Lab values
- Pregnancy or lactation (Pregnancy status will be determined via serum blood test \& lactation will be determined via self-report),
Other
- Initiation of immunosuppressive or antimalarial treatment within 3 months of baseline,
- Initiation of anifrolumab within 3 months of baseline
- Initiation of belimumab within 6 months of baseline,
- Fibromyalgia,
- Current tobacco or nicotine user (to limit potential confounding effects of exposure to nicotine),
- Intra-articular cortisone injections within 28 days of the start of study,
- Inability to comply with study and follow-up procedures.
Who the study is looking for
- SLE (defined by the ACR or SLICC criteria),
- Musculoskeletal pain ≥ 4 on a non-anchored VAS 10 cm scale,
- BILAG C or greater on the Musculoskeletal Domain of the BILAG 2004,
- If on corticosteroids, the dose must be stable and ≤ 10 mg/day (prednisone or equivalent) for at least 14 days before baseline,
- If on background immunosuppressive treatment the dose must be stable for at least 28 days before baseline,
- If on NSAIDS, the dose must be stable for at least 7 days before baseline and the subject must be willing not to change the dose during the trial (except for toxicity),
- Able and willing to give written informed consent and comply with the requirements of the study protocol.
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Feinstein Institutes for Medical Research Coordinator of this site? Confirm its status | Manhasset | United States | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.