Skip to content

Studying the effect of transcutaneous spinal cord stimulation in patients with neurogenic shock caused by trauma to sub-axial cervical spine.

Role of transcutaneous spinal cord stimulation (TSCS) in neurogenic shock in sub-axial cervical spinal cord injury - NIL

Status
Active, not recruiting
Phases
Phase 1Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/08/057094
Enrollment
10
Registered
2023-08-30
Start date
Unknown
Completion date
Unknown
Last updated
2023-09-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: G89-G99- Other disorders of the nervous system

Interventions

Intervention1: Transcutaneous spinal cord stimulation (procedure): frequency – 30 Hz to 10KHz
Stimulus – Monophasic/biphasic stimulation, starting with low stimulation intensity, pulse width and frequency and titrating upwards till maximum tolerable threshold or till favourable clinical improv
if desirable clinical improvement/intolerable side effects (pain, arrhythmia, breathlessness) – whichever is earlier Control Intervention1: NA: NA

Sponsors

Priyadharshan KP
Lead Sponsor
Kodeeswaran M
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: Patients of all age groups presenting with sub-axial spinal cord injury with neurogenic shock

Exclusion criteria

Exclusion criteria: 1) Presence of other factors contributing to shock (hypovolemic, septic, distributive), till appropriate correction 2) Co-morbidities like diabetes mellitus, hypertension, coronary artery disease, COPD, Asthma, endocrine abnormalities, congenital disorders, epilepsy, neurological conditions 3) Patient under the influence of drugs/alcohol intoxication etc.. 4) Pregnancy 5) Loss of skin at the site of electrode application 6) Associated other system injuries– (till addressed – example: Pneumothorax- till ICD insertion and lung expansion, etc.) 7) Presence of other implants – pacemakers, cochlear implants etc…

Design outcomes

Primary

MeasureTime frame
Heart rate Systolic & Diastolic blood pressure Electrocardiogram Echocardiography Bilateral lower limb arterial & venous doppler EMG bilateral upper & lower limb Ventilatory parameters, Total respiratory cycle time, Tidal volume, FVC Timepoint: At the time of diagnosis of neurogenic shock in patient included in the study

Secondary

MeasureTime frame
Motor/Sensory/Autonomic clinical examinationTimepoint: At the time of diagnosis of neurogenic shock in patient included in the study

Countries

India

Contacts

Public ContactPriyadharshan KP

Government Kilpauk Medical College

jerryno2@gmail.com08056452431

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026