Effects of Minocycline on Patients With Ischemic Stroke Undergoing Intravenous Thrombectomy
NCT05487417 · Status: RECRUITING · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 180
Last updated 2025-07-24
Summary
Minocycline is the second generation of tetracycline. Because of its lipophilicity, it has high penetrance of blood-brain barrier. Animal model studies have shown that minocycline can reduce cerebral damage after ischemic stroke, and its mechanism involves multiple molecular pathways, such as antioxidant, anti-inflammatory, anti apoptotic pathways, and protection of blood-brain barrier. Clinical studies have also shown that minocycline can significantly improve 3-month National Institute of Health Stroke Scale (NIHSS) and modified Rankin Scale (mRS) of patients with ischemic stroke, indicating that minocycline is a potential neuroprotective drug. Minocycline is believed to protect the blood-brain barrier, thereby reducing the ischemia-reperfusion injury caused by mechanical thrombectomy. However, whether minocycline can become a synergistic treatment method of mechanical thrombectomy, there is no clinical research in this area at present. Therefore, investigators carry out the study on the effect of minocycline in patients with acute anterior circulation ischemic stroke after mechanical thrombectomy, and plan to enroll 180 patients. To explore the safety and effectiveness of minocycline in patients with acute ischemic stroke after thrombectomy.
Conditions
- Ischemic Stroke, Acute
Interventions
- DRUG
-
Minocycline
Minocycline is a tetracycline antibiotic. Previous studies have confirmed that its application in stroke patients has good efficacy and safety, suggesting that it could become a synergistic treatment of mechanical thrombectomy.
Sponsors & Collaborators
-
Xi'an No.3 Hospital
collaborator OTHER_GOV -
Xi'an Gaoxin Hospital
collaborator OTHER -
First People's Hospital of Xianyang
collaborator OTHER -
Xi'an XD Group Hospital
collaborator UNKNOWN -
Baoji High-tech Hospital
collaborator UNKNOWN -
Weinan Central Hospital
collaborator OTHER -
Xi'An Daxing Hospital
collaborator UNKNOWN -
Yan'an University Xianyang Hospital
collaborator UNKNOWN -
The First Hospital of Yulin
collaborator UNKNOWN -
Northwest University First Hospital
collaborator UNKNOWN -
Jingyang County Hospital
collaborator UNKNOWN -
Yulin No.2 Hospital
collaborator OTHER -
Yan'an people's Hospital
collaborator UNKNOWN -
Yuncheng Central Hospital
collaborator OTHER -
Second Affiliated Hospital of Xi'an Jiaotong University
collaborator OTHER -
Xi'an No.9 Hospital
collaborator UNKNOWN -
First Affiliated Hospital Xi'an Jiaotong University
collaborator OTHER -
Pucheng County Hospital
collaborator UNKNOWN -
Xijing Hospital
lead OTHER
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- SINGLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 85 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2022-11-01
- Primary Completion
- 2025-06-10
- Completion
- 2025-09-10
Countries
- China
Study Locations
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