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TCM Clinical Practice Rehabilitation of Post-stroke Spasticity

Traditional Chinese Medicine Clinical Practice Rehabilitation of Post-stroke Spasticity

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03054974
Enrollment
1208
Registered
2017-02-16
Start date
2013-01-31
Completion date
2018-12-31
Last updated
2017-02-16

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

Conditions

Stroke

Keywords

Stroke, Traditional Chinese Medicine, Rehabilitation

Brief summary

The purpose of this study is to determine the effectiveness,safety and Input-output ratio of chinese traditional treatment in spasm after stroke,both in massage and herbal medicine bathing.

Detailed description

A Muti-center randomized controlled study with large samples to observe improvement of motor function,severity of spasm,ADL(activity of daily lives),by standardized protocols of TCM techniques(massage and herbal bathing) combined with conventional rehabilitation on spasm after stroke in 1 month.Modified Ashworth scale,Fugl-Meyer Index and Modified barthel Index were used for spasm,motor function and ADL.And also the follow up research within 3 months and 6 months focus on the efficacy duration of TCM on spasm.Try to find suitable timing for intervention on spasm by CTM(Massage and herbal medicine bathing)and the connection between spasm severity and treatment efficacy.

Interventions

OTHERModern rehabilitation treatment

PT 1 hour per day and OT 30min per day

OTHERModern rehabilitation &TCM

Traditional Chinese Medicine, including massage and medicated bath

OTHERmodern rehabilitation &Baimai Ruangao

modern rehabilitation treatment with Baimai Ruangao and massage

OTHERmodern rehabilitation &Tibetan medicine

modern rehabilitation treatment and Tibetan medicine(medicated bath with wuweiganlu and rub with baimairuangao)

Sponsors

The First Affiliated Hospital with Nanjing Medical University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
Yes

Inclusion criteria

* According to the diagnostic criteria of stroke and diagnosed by CT or MRI * Patient must be between the ages of 18 and 85 years. * All patients were examined at least 1 month after stroke and less than 12 months. * At least a set of spasmous muscles' level ≥1+ of dysfunctional extremities (modified Ashworth scale) * Body movement function decreased significantly. * The doses and kinds of anticonvulsant drugs should be used stable for more than 1 month if they are used * Patient must understand and be willing, able and likely to comply with all study procedures. * Patient must be able to give voluntary written informed consent.

Exclusion criteria

* Significant cognitive defects(MMSE\<16),unable to finish the Fugl-Meyer scale,etc.. * Other significant limb diseases such as fracture, severe arthritis,amputation * Joint contracture formation * Patients with significant pain and swelling suffering from complex regional syndrome after acute stroke * Accept botulinum toxin or alcohol nerve block 3 months prior to the start of the experiment * Patients need nerve block at any point of time during the whole experiment procedure. * Serious cardiac,hepatic or renal insufficiency and patients with shock. * Limb skin of patients who need medicated is visible wound. * Patients with cancer or pregnancy * Patients who participate in other clinical studies within 6 months

Design outcomes

Primary

MeasureTime frameDescription
Modified Ashworth Scale6 monthsthe common used clinical measurement to assess the levels of limb spasticity

Secondary

MeasureTime frame
Fugl-Meyer Moter Assessment6 months

Other

MeasureTime frame
Barthel Index6 months

Countries

China

Contacts

Primary Contactli jianan, Doctor
lijianan@carm.org.cn+862583318752

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026