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Vagal Nerve Stimulation to Treat Disorders of Consciousness
Sponsor: Fondazione IRCCS San Gerardo dei Tintori
Summary
This interventional study aims to assess the clinical efficacy of transcutaneous auricular vagal nerve stimulation (taVNS) against sham stimulation on the recovery of consciousness in patients with disorders of consciousness. The main question it aims to answer is: will taVNS improve patients' behavioral scores or will it produce an improvement in the diagnosed level of consciousness? Researchers will compare the results with non-stimulated unconscious patients to see if the re-gain of consciousness is faster in the treated group. Participants will undergo taVNS stimulation using the Parasym device or sham stimulation will be applied from the time of enrolment. Active stimulations will be carried out for 60 minutes twice daily during the acute phase and daily during the rehabilitation phase.
Official title: Transcutaneous Vagal Nerve Stimulation to Treat Disorders of Consciousness
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
106
Start Date
2025-09-01
Completion Date
2028-09-01
Last Updated
2025-07-22
Healthy Volunteers
No
Conditions
Interventions
stimulated group
Participants will be randomly assigned to receive either taVNS applied to the tragus of the ear or a sham stimulation from the time of randomization for 90 days. Active simulations will be carried out daily using the Parasym device for 60 minutes twice daily during the acute phase (two sessions, one in the morning and one in the afternoon), and once daily (single session) during the rehabilitation phase. The stimulation waveform includes trains of pulses with widths of 200 µs and repetition rate of 20 Hz (Nurosym proprietary waveform); current delivery will be set at a predefined therapeutic level below 0.25 W/cm² (Watts per centimeter squared), that being the defined risk threshold for a thermal burn. The device adjusts stimulation intensity at 0.8 mA steps; the starting intensity will be set at 16 mA (level 20).
Sham (No Treatment)
The sham stimulation involves placing the electrode on the same site without delivering any electrical current. The device will be applied to the tragus without electrical current delivered from the time of randomization for 90 days (i.e., the time of randomization coincides with the first stimulation session).
Locations (11)
ASST degli Spedali Civili di Brescia
Brescia, BS, Italy
Fondazione IRCCS San Gerardo dei Tintori
Monza, MB, Italy
ASST Papa Giovanni XXIII
Bergamo, Italy
ASST Lariana Ospedale S. Anna
Como, Italy
Ospedale Policlinico San Martino IRCCS
Genova, Italy
ASST Grande Ospedale Metropolitano Niguarda
Milan, Italy
Azienda Ospedaliera Università di Padova
Padova, Italy
Azienda Ospedaliera Universitaria di Parma
Parma, Italy
Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Roma, Italy
Humanitas Research Hospital
Rozzano, Italy
ASST Sette Laghi Ospedale di Circolo e Fondazione Macchi
Varese, Italy