Skip to content

The Study on the Therapeutic Effects of VEGF and NFL-based Macherin Capsule for Post-Ischemic Stroke Soft Paralysis

A Clinical Study on the Therapeutic Efficacy of Strychnos nux-vomica Capsules for Flaccid Paralysis after Ischemic Stroke Based on VEGF and NFL

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ITMCTR
Registry ID
ITMCTR2026000410
Enrollment
Unknown
Registered
2026-02-25
Start date
2026-01-01
Completion date
Unknown
Last updated
2026-03-02

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

Conditions

Ischemic Stroke with Hemiparesis

Interventions

Control Group :Based on syndrome differentiation and treatment, conventional treatment was administered according to the China Guidelines for Stroke Prevention and Treatment (2021 Edition), and Maqia
Experimental Group:The experimental group received conventional treatment as in the control group, combined with oral administration of Maqianzi capsules. The starting dose was 0.2 g, taken twice dail

Sponsors

The First Affiliated Hospital of Zhejiang Chinese Medical University (Zhejiang Provincial Hospital of Chinese Medicine)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1: Patients with first-onset ischemic stroke. 2: Patients diagnosed with ischemic stroke according to both traditional Chinese medicine and Western medicine criteria, in the flaccid paralysis stage, with muscle strength = grade 3 in the affected limb and decreased muscle tone or weakened reflexes. 3: Male or female patients aged 18–80 years (inclusive). 4: Disease duration =6 months from stroke onset. 5: Stable vital signs, clear consciousness, and ability to cooperate with examinations and treatment. 6: Fully informed of the study and voluntarily signed written informed consent.

Exclusion criteria

Exclusion criteria: 1: Patients who do not meet the inclusion criteria or have entered the spastic stage with increased muscle tone. 2: Patients with severe dysfunction of major organs such as the heart, lungs, liver, or kidneys, or other serious systemic diseases. 3: Patients with limb dysfunction caused by other diseases, or with significant upper-limb trauma or fractures affecting functional assessment. 4: Patients with extreme physical weakness, pregnant women, or breastfeeding women. 5: Patients with significant consciousness disturbance, inability to cooperate with the study, or incomplete clinical data. 6: Patients with transient ischemic attack (TIA), subarachnoid hemorrhage (SAH), or neurological deficits confirmed to be caused by non-stroke etiologies.

Design outcomes

Primary

MeasureTime frame
National Institutes of Health Stroke Scale (NIHSS);

Secondary

MeasureTime frame
Serum Vascular Endothelial Growth Factor (VEGF);Serum Neurofilament Light Chain (sNFL);Modified Ashworth Scale (MAS) for Spasticity;Muscle Strength Grading (0–5 scale);Modified Rankin Scale (mRS);Modified Barthel Index (MBI);Liver and Kidney Function,Complete Blood Count (CBC),Electrocardiogram (ECG),Adverse Reactions;

Countries

China

Contacts

Public Contactlinzhu

The First Affiliated Hospital of Zhejiang Chinese Medical University (Zhejiang Provincial Hospital of Chinese Medicine)

1009574297@qq.com+8613616519749

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Mar 14, 2026