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

No results posted yet for this study

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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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05487417 on ClinicalTrials.gov