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To explore the clinical study of Jieyu prescription in the treatment of post-stroke depression based on the diversity of intestinal flora

To explore the clinical study of Jieyu prescription in the treatment of post-stroke depression based on the diversity of intestinal flora

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300068128
Enrollment
Unknown
Registered
2023-02-08
Start date
2023-02-10
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

Post stroke depression

Interventions

Paroxetine hydrochloride tablet group:Take paroxetine hydrochloride tablets orally, 1 tablet each time, once a day
Paroxetine hydrochloride tablet+self-designed Jieyu prescription group:On the basis of the treatment in the control group, the observation group drank self-designed Jieyu prescription: 1 dose a day, d
Cognitive behavioral therapy+self-designed Jieyu prescription group:On the basis of the treatment in the control group, the observation group drank self-designed Jieyu prescription: 1 dose a day, drin
Stroke patients without depression:Placebo treatment

Sponsors

Wenzhou Hospital of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: ? At the same time comply with the prescribed diagnostic standards of Chinese and western medicine; ? Those who agree and sign the informed consent; ? Age 18-80 years old; ? Have the ability of communication and expression; ? Hamilton Depression Scale (17 items) score in 8-24; ? Secondary to acute cerebrovascular disease 2 weeks later to 1 year.

Exclusion criteria

Exclusion criteria: ? Patients with severe aphasia or cognitive impairment;? People with a history of mental illness or suicide attempts; ? Unwilling to take Chinese medicine; ? Patients with digestive tract diseases that may affect the intestinal flora; ? Patients taking antibiotics in recent 2 months; ? At the same time accept other clinical trial patients; ? Hamilton Depression Scale (17 items) score =25: may have major depression patients.

Design outcomes

Primary

MeasureTime frame
Hamilton Depression Scale (17 items);TCM syndrome integration;6/5000 Self-Rating Depression Scale(SDS);

Secondary

MeasureTime frame
Motor function (short Fugl-Meyer) score;Activities of Daily Living Score (ADL); Hamilton Anxiety Scale (HAMA);Intestinal flora;

Countries

China

Contacts

Public ContactZhi Yinghao

Wenzhou Hospital of Traditional Chinese Medicine

43914515@qq.com+86 13758472924

Outcome results

None listed

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