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Surgery to reopen blocked large brain arteries in acute stroke

Tests combined surgery to reopen blocked large brain arteries in adults with acute stroke.

Key facts

Who runs it
Tianjin Huanhu Hospital
Where
Tianjin, ChinaSee the site
Trial code
Registry title
Combined Recanalization Therapy for Acute Large Vessel Occlusion Stroke
Status
Recruiting
People taking part
64 people, planned
Started
1 Dec 2024
Expected to end
30 Nov 2026
Type of study
Interventional, 2 groupsOne group gets no study treatment, for comparison.
Treatments tested
  • Surgery
Record updated
11 August 2025

Who can take part

AI summary

From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.

The trial is looking for adults aged 18-75 with a sudden stroke from a blocked large brain artery, where a clot-removal procedure did not reopen the vessel.

Age
18 to 75 years
Sex
All sexes can join.
Disease stage
Stroke from a blocked middle cerebral artery (MCA), with or without a blocked internal carotid artery (ICA). A clot-removal procedure (thrombectomy) failed, with a TICI score of 0-1. ASPECTS of 6 or higher. Time from onset to surgery expected to be 24 hours or less. For stroke noticed after waking, there must be a mismatch between the damaged brain area and the area still at risk.
Earlier treatment
Must have had a clot-removal procedure that did not work. Must not have had earlier brain or neck artery bypass surgery.

Main reasons for not taking part

  • Bleeding vessel disease such as an aneurysm or vascular malformation
  • Heart attack, unstable angina or heart failure in the last 6 months
  • Pregnancy or the period around birth
  • Blood clotting disorder, or platelets below 100×10^9/L
  • Uncontrolled diabetes or uncontrolled high blood pressure

The registry criteria, word for word

Show all 22 criteriaShow less

Who can take part

  • Age: 18-75
  • According to the current guidelines, there is a MT indication
  • Before stroke, mRS ≤2
  • ASPECTS ≥6
  • MCA occlusion, with or without ICA occlusion
  • MT unsuccessful, TICI score 0-1
  • Time from onset to craniotomy expected to be 24 hours or less
  • Post-awakening stroke with mismatch between the infarct zone and the penumbra zone

Who cannot take part

  • unstable angina or myocardial infarction, congestive heart failure within the previous 6 months
  • previous treatment with intracranial or extracranial vascular bypass surgery
  • Received a clinical trial drug or device within 30 days prior to screening, or is participating in another clinical trial
  • Comorbid hemorrhagic vascular disease such as intracranial aneurysm or vascular malformation or other planned cerebrovascular surgery that may alter cerebral hemodynamics or lead to stroke
  • Hematologic disorders resulting in coagulation disorders
  • Combination of other diseases with a life expectancy of less than 2 years; and
  • Uncontrolled hypertension with sitting systolic blood pressure >180 mmHg or sitting diastolic blood pressure >110 mmHg
  • other diseases or medical history that, in the investigator's judgment, may affect the efficacy or safety evaluation of this study
  • allergy to iodine or X-ray contrast media, creatinine >3.0 mg/dl or other contraindications to arteriography
  • Uncontrolled diabetes mellitus, fasting blood sugar (FBS) >16.7 mmol/L
  • Severe hepatic dysfunction, defined as serum alanine aminotransferase (ALT) and/or alanine aminotransferase (AST) >3 times the upper limit of normal
  • Platelets <100×109 /L
  • Pregnancy or perinatal period
  • contraindication to general anesthesia or craniotomy

Check if you might fit

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 75 years old?

Where in China

  • Tianjin Huahu HospitalTianjin, ChinaContact: Gao KaimingTaking people

About the trial

What the trial wants to find out

The purpose of this clinical trial is to evaluate the efficacy and safety of combined recanalization therapy in patients who cannot be recanalized by acute large vessel occlusive stroke. The main questions it aims to answer are:

Read full original descriptionShow less

1、Proportion of subjects with mRs score of 0-1 at 90 days after surgery

Participants will:

1、In acute large vessel occlusive stroke, if traditional means cannot be recanalized, combined recanalization surgery (including arteriotomy and thrombectomy, cerebrovascular bypass surgery) is performed.

The 2 groups in the trial

  • experiment group(surgical treatment)Treatment being tested

    Treatment: Surgery

  • control group(conservative therapy)No study treatment, for comparison

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

Print a page for my doctor

Data and sources

Registry record
Listed on ClinicalTrials.gov.
Official title
Combined Recanalization Therapy for Acute Large Vessel Occlusion Stroke
Plain-language title
Surgery to reopen blocked large brain arteries in acute strokeGenerated from the registry record. The registry title is the official one.
AI summary
From the trial's eligibility criteria. Read by machine on 12 November 2026.
Fit questions
Built from NCT07115511, who can take part
Record updated
11 August 2025