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Study on Shengqing Dangzhuo Formula Regulating Intestinal Microecology Intervention for Post-Stroke Cognitive Impairment Based on the Brain-Gut Axis

Study on Shengqing Dangzhuo Formula Regulating Intestinal Microecology Intervention for Post-Stroke Cognitive Impairment Based on the Brain-Gut Axis

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400089926
Enrollment
Unknown
Registered
2024-09-19
Start date
2024-06-05
Completion date
Unknown
Last updated
2024-09-23

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

Conditions

Stroke

Interventions

Experimental group:Formula "Shengqing Dangzhuo" combined with Meclofenoxate Hydrochloride
Control group:Meclofenoxate Hydrochloride

Sponsors

Shijiazhuang People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Meets diagnostic criteria for ischemic stroke/hemorrhagic stroke. 2. In the recovery phase of ischemic stroke/hemorrhagic stroke. 3. Meets diagnostic criteria for post-stroke cognitive impairment: 1) Clear diagnosis of stroke. 2) Presence of cognitive impairment: Patients' self-reports, reports from informants, or clinical judgment by experienced clinicians indicate cognitive impairment occurring after stroke, and neuropsychological evidence confirms impairment in one or more cognitive domains or evidence of cognitive decline compared to previous status. 3) Temporal relationship between stroke and cognitive impairment: Occurs after stroke and persists for 3-6 months. 4. Age between 18 and 80 years. 5. Patient is conscious, vital signs are stable, compliance is good, and able to complete assessment scales. 6. Voluntary participation and signing of informed consent form.

Exclusion criteria

Exclusion criteria: 1. Individuals with cognitive impairment caused by conditions such as Alzheimer's disease, Parkinson's syndrome, brain tumors, metabolic or infectious diseases, or other etiologies. 2. Patients with severe underlying conditions such as severe hepatic or renal dysfunction, severe congestive heart failure, or significant coagulation abnormalities. 3. Patients unable to complete various assessment scales due to conditions such as aphasia. 4. Pregnant and lactating women. 5. Patients with a history of allergies.

Design outcomes

Primary

MeasureTime frame
MMSE ;MoCA;Intestinal Microbiota;Intestinal Metabolomics;CCS;

Secondary

MeasureTime frame
NIHSS;Fugl-meyer;CSBM;

Countries

China

Contacts

Public ContactJianchao Xu

Shijiazhuang People's Hospital

xjc_listening@163.com+86 180 3383 5852

Outcome results

None listed

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