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Assessment of change in pain relief in subjects with neuropathic pain due to diabetes using magnetic stimulation applied across the scalp

Effect of repetitive Transcranial magnetic stimulation for resistant diabetic neuropathic pain: A pilot study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/12/099801
Enrollment
10
Registered
2025-12-24
Start date
Unknown
Completion date
Unknown
Last updated
2026-01-12

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

Conditions

Health Condition 1: G64- Other disorders of peripheral nervous system

Interventions

Intervention1: Transcranial Magnetic Stimulation: Repetitive pulse mode, Frequency 10Hz, Pulse per train 50, Number of trains 15, Pulse duration 5seconds, Interpulse duration 30seconds, Test duration

Sponsors

Dr Rajeswari Aghoram
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Type 2 diabetic patients with diabetic neuropathy as defined by toronto clinical neuropathy score more than 9 and resistant pain defined as visual analogue score in the last one week more than 4 while being on at least one pain relief medication.

Exclusion criteria

Exclusion criteria: a) Any active ulcer or inflammation b) Any other cause that can explain the pain like fractures c) Past history of seizure or epilepsy in self or family.

Design outcomes

Primary

MeasureTime frame
To estimate the change in Visual analogue score (VAS) Timepoint: It will be estimated following 5 sessions of Repetitive Transcranial Magnetic Stimulation and also at the end of 2 weeks.

Secondary

MeasureTime frame
To estimate the change in visual analogue score at the end of 5 sessions, and at the end of 1 month and 2 month Timepoint: Visual analogue score is estimated at end of 5 sessions, 1 month and 2 months;To evaluate safety and tolerability of repetitive transcranial magnetic stimulation in this patient populationTimepoint: It will be estimated at end of 1 month;To evaluate its effect on nerve conduction parameters, Patient global impression of change and DN4 scale.Timepoint: Effect on Nerve conduction parameters will be estimated at end of 2 weeks, Patient global impression of change at end of 1 month and DN4 scale at end of 5 sessions, 2 weeks, 1 month and 2 months

Countries

India

Contacts

Public ContactDr Rajeswari Aghoram

Jawaharlal Institute of Postgraduate Medical Education and Research

balakumarjayavel011@gmail.com7339316222

Outcome results

None listed

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