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The efficacy of high-frequency repetitive transcranial magnetic stimulation on The efficacy of high-frequency repetitive transcranial magnetic stimulation on central post stroke pain

The efficacy of high-frequency repetitive transcranial magnetic stimulation on The efficacy of high-frequency repetitive transcranial magnetic stimulation on central post stroke pain

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500113081
Enrollment
Unknown
Registered
2025-11-24
Start date
2024-11-29
Completion date
Unknown
Last updated
2025-12-01

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

Conditions

Central post stroke pain

Interventions

Group A:Sham rTMS stimulation
Group B:5HzrTMS
Group C:10HzrTMS
Group D:20HzrTMS

Sponsors

Tangdu Hospital, the Fourth Military Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to No maximum

Inclusion criteria

Inclusion criteria: 1 Meeting the diagnostic criteria of central pain after stroke; 2 Age >= 45 years old, both sexes; 3 Stroke duration 1 week to 6 months (hemorrhagic stroke 2 weeks to 6 months); The duration of central pain was = 4; Montreal Cognitive Assessment score >= 26; ? All cases were the first onset. ? understanding and willing to participate in the clinical trial and provide signed informed consent.

Exclusion criteria

Exclusion criteria: 1. Excluding pain or paresthesia caused by other than central pain after stroke; 2. patients with cardiac pacemaker or other metal implants in the body; 3. acute stage of cerebral hemorrhage (< 2 weeks); The patients with intracranial space occupying or craniocerebral trauma 4. had a history of seizures, 6. serious lesions in liver, kidney and other organs, complicated with cardiovascular diseases or intracranial tumors, 6. abnormal consciousness or complicated with or complicated with mental diseases, 7. used analgesics, anti-anxiety and depression drugs within the past 1 month.

Design outcomes

Primary

MeasureTime frame
Short-Form McGill Pain Questionnaire, SF-MPQ;Pittsburgh Sleep Quality Index, PSQI;

Secondary

MeasureTime frame
Hamilton Anxiety Rating Scale, HAMA;Hamilton Depression Rating Scale - 17 items, HAMD-17;

Countries

China

Contacts

Public ContactLiu Rui

Tangdu Hospital, the Fourth Military Medical University

speciallr@163.com+86 150 0299 5399

Outcome results

None listed

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