Evaluating the efficacy of rTMS in managing somatosensory deficits post ischemic stroke: a randomised and sham-controlled study

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2200059098

Enrollment

Unknown

Registered

2022-04-24

Start date

2022-04-11

Completion date

Unknown

Last updated

2024-02-11

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

Conditions

somatosensory deficits post stroke

Interventions

10 Hz:10 Hz rTMS over lesioned S1

1 Hz:1 Hz rTMS over ipsilateral S1

Eligibility

Sex/Gender

All

Age

18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: a. unilateral ischemic stroke. b. somatosensory deficits caused by ischemic stroke c. 18-80 years old. d. regular stroke medicines. e. rTMS illegible f. capable of fulfilling assessments

Exclusion criteria

Exclusion criteria: Exclusion criteria: a. not able to receive rTMS. b. severe mental disorders: HAMD = 35 or HAMA = 29. c. aphasia or cognitive disorders: MMSE = 24. d. not able to fulfil assessments e. severe disorders caused by others, e.g. tumour. f. mRS > 2. g. severe heart or lung misfunctioning or extremely weak h. somatosensory deficits not caused by ischemic stroke, e.g. diabetes pain

Design outcomes

Primary

Measure	Time frame
Fugl-Meyer and Lindmark Assessment;	—

Countries

China

Contacts

Public ContactXianwei Che

Affiliated Hospital of Hangzhou Normal University

xwcheswu@gmail.com+86 18072852895

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 5, 2026