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Clinical Research of modified Dihuang Yinzi Decoction combined Swallowing Rehabilitation and videofluoroscopy on Post-stroke Dysphagia patients : a pilot trial

Clinical Research of modified Dihuang Yinzi Decoction combined Swallowing Rehabilitation and videofluoroscopy on Post-stroke Dysphagia patients : a pilot trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-14004235
Enrollment
Unknown
Registered
2014-01-26
Start date
2014-02-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

post-stroke dysphagia

Interventions

herb treatment group:modified Dihuang Yinzi Decoction
control:Placebo and training

Sponsors

Wenzhou Chinese Medicine Hospital of Zhejiang Chinese Medicine University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: Dysphagia symptoms appeares within one months to six months after stroke; the symptoms are in compliance with the stroke diagnostic standards and a clearly VFSS result; MMSE scale >26 scores, patients are conscious, stable life sign and able to cooperate for examination and treatment; aged 18-85 years old; signed the informed consent

Exclusion criteria

Exclusion criteria: The cause of the dysphagia is not related with stroke; Patients with consciousness disorder; unable life sign and accompanied with serious heart,kidney,etc., dysfunctions; not compliance with examination and treatment are excluded.

Design outcomes

Primary

MeasureTime frame
Baseline data;Swallowing Rehabilitation improvement diagnosted by videofluoroscopy;adverse event;—

Countries

China

Contacts

Public ContactJianping Huang

Wenzhou Chinese medicine Hospital

wzszyy_zwz@126.com+86 13738718777

Outcome results

None listed

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