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Clinical Trials in China / NCT04673643
Recruiting Phase 2

Transcutaneous Auricular Vagus Nerve Stimulation in Dry Eye Disease

NCT04673643 · tracked via the Priya Life Science China tracker
Sponsor
Beijing Tongren Hospital
Phase
Phase 2
Started
2021-07-01
Last updated
2024-09-19

Condition(s) studied

Dry Eye Disease

Investigational drug(s) / intervention(s)

Transcutaneous Auricular Vagus Nerve StimulationHyaluronic acid eye drops

Transcutaneous Auricular Vagus Nerve Stimulation: taVNS device (Elmmedicare, EC100, Shenzhen, China) was used to apply stimulation for patients. Stimulation parameters comprised an electrical current of 1 mA at a frequency of 20 Hz, with a waveform width of 1 ms. Repurposed off-the-shelf devices were utilized for this purpose, with the stimulator generating single square-wave pulses lasting 1 ms each. Enhancing conductivity was achieved by wiping the ear with tap water. The electrodes were placed on the cymba conchae and concha around the affected ear, which is the region of rich vagus nerve branch distribution. Patients in control group were applied using the same stimulator, stimulation parameters and same sessions. However, the electrodes were placed on the antihelix around the affected ear, which is the region of few vagus nerve branch distribution.

Hyaluronic acid eye drops: Participants in both groups received hyaluronic acid eye drops (HYLO COMOD® eye drops, Ursapharm, Ltd., Germany) with the treatment of 3 times a day.

Study summary

Objective: To evaluate the effect of transcutaneous auricular vagus nerve stimulation (taVNS) for the patients with dry eye disease with meibomian gland dysfunction.

Methods: We enrolled 256 patients at Beijing Tongren Hospital. Patients completed questionnaires at baseline, 1 month, 3 months, and 6 months.OSDI score, TBUT, Schirmer I, tCFS, MGD score, and psychological status to evaluate the therapeutic effects. A difference of P \< 0.05 was considered statistically significant.

Eligibility

Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
No
Inclusion Criteria: 1. Age \>=18 and Age \<=75. 2. Clinical diagnosis of dry eye disease. Exclusion Criteria: 1. History of depression, tumors, thyroid disease, diabetes, cardiac diseases. 2. History of phthalmology surgery. 3. Pregnant or lactating women.

Primary outcome measure(s)

Trial sites (2)

FacilityCityRegionStatus
Beijing Tongren Hospital Beijing China Recruiting
Wu Dong Beijing China Completed

More Beijing Tongren Hospital trials in China

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT04673643 on ClinicalTrials.gov ↗ ← All trials in China