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Exploration and Research on the clinical mechanism of Longxue Tongluo Capsule in the Treatment of the Recovery Period of Acute Cerebral Infarction

Exploration and Research on the clinical mechanism of Longxue Tongluo Capsule in the Treatment of the Recovery Period of Acute Cerebral Infarction

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025001098
Enrollment
Unknown
Registered
2025-06-03
Start date
2025-06-28
Completion date
Unknown
Last updated
2025-06-24

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

Conditions

The recovery period of acute cerebral infarction

Interventions

Experimental Group 1:Longxue Tongluo Capsules, oral, 2 capsules each time, three times a day
Control group:Enteric-coated aspirin tablets, oral, 1 tablet each time, once a day
Experimental Group 2:Longxue Tongluo Capsules, oral, 2 capsules each time, three times a day
Enteric-coated aspirin tablets, oral, 1 tablet each time, once a day

Sponsors

Lianyungang First People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 120 Years

Inclusion criteria

Inclusion criteria: (1) Meet the diagnostic criteria for cerebral infarction in Western medicine; (2) The course of this illness does not exceed 28 days. (3) Agree to participate in this study and sign the informed consent form.

Exclusion criteria

Exclusion criteria: (1) Patients with progressive stroke transient ischemic attack cerebral hemorrhage after cerebral infarction and cerebral arteritis; (2) Patients with concurrent brain tumors brain trauma brain parasitic diseases etc. (3) Pregnant or lactating women; (4) Those who are allergic to the known components of the drug used in this study; (5) Active ulcers and those with a tendency to bleed; (6) Patients whom the researchers consider unsuitable to participate in this study.

Design outcomes

Primary

MeasureTime frame
Analysis of platelet aggregation function;Thromboelastography;Four items of thrombosis;

Secondary

MeasureTime frame
The change of NIHSS score after 28 days of medication compared with the baseline;The proportion of no significant disability (grade 0-2) on the modified Rankin scale after 28 days of medication;

Countries

China

Contacts

Public ContactHe Mingli

Lianyungang First People's Hospital

lyghml@163.com18961326515

Outcome results

None listed

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