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A prospective cohort study of XingNao JieYu Capsule in the treatment of post-stroke depression with phlegm stasis junction

A prospective cohort study of XingNao JieYu Capsule in the treatment of post-stroke depression with phlegm stasis junction

Status
Recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400081813
Enrollment
Unknown
Registered
2024-03-13
Start date
2023-08-24
Completion date
Unknown
Last updated
2024-03-18

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

Conditions

Poststroke depression

Interventions

Exposed group:Oral XingNao JieYu capsules+Conventional western medicine treatment for post-stroke depression
Non-exposed group:Conventional western medicine treatment for post-stroke depression

Sponsors

Affiliated Hospital of Shaanxi University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Meet the Western medical diagnostic criteria for post-stroke depression; (2) Meet the diagnostic criteria of traditional Chinese medicine phlegm and stasis syndrome; (3) Those who are assessed by the HAMD-17 scale and have a score between 7 and 24 points; (4) Age 18-75 years old, no gender limit; (5) Sign the informed consent form, be able to take medication regularly according to the doctor's instructions and follow up regularly.

Exclusion criteria

Exclusion criteria: (1) Previous history of mental illness or family history of mental illness; (2) Patients with severe cardiovascular, hepatic and kidney, hematopoietic system and endocrine immune system diseases; (3) Those with dementia, aphasia, cognitive dysfunction and inability to cooperate with the completion of the scale and other related examinations; (4) Those with a history of drug abuse (including sleeping pills) or alcohol abuse; (5) Those with allergies and allergies to a variety of drugs; (6) Those who are participating in or have participated in other clinical research trials within the past 30 days

Design outcomes

Primary

MeasureTime frame
Hamilton Depression Scale-17,HAMD-17;

Secondary

MeasureTime frame
Self-rating depression scale,SDS;The World Health Organization Quality of Life,WHOQOL-BREF;NIH Stroke Scale,NIHSS;Traditional Chinese Medicine Syndrome Integral Scale;

Countries

China

Contacts

Public ContactYan Yongmei

Affiliated Hospital of Shaanxi University of Chinese Medicine

13609216551@163.com+86 136 0921 6551

Outcome results

None listed

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