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NOT YET RECRUITING
NCT07077135
NA

Vagal Nerve Stimulation to Treat Disorders of Consciousness

Sponsor: Fondazione IRCCS San Gerardo dei Tintori

View on ClinicalTrials.gov

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

Interventions

DEVICE

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).

DEVICE

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