Actively Recruiting
Early Prophylactic Decompressive Hemicraniectomy Following Endovascular Therapy in Large Hemispheric Infarct Trial
Led by Xuanwu Hospital, Beijing · Updated on 2026-01-26
380
Participants Needed
2
Research Sites
204 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Early Decompressive Hemicraniectomy for High-Risk Large Ischemic Core Stroke Post-EVTAcute Ischemic Stroke (AIS), particularly Anterior Circulation Large Vessel Occlusion (LVO), is a major cause of global disability and death. While endovascular thrombectomy (EVT) is the standard first-line treatment for LVO, outcomes remain poor in patients with large ischemic cores (ASPECTS ≤5). Despite high recanalization rates (\>90%), only 14-30% achieve functional independence (mRS 0-2) at 90 days, with 33-50% dead or severely disabled (mRS 5-6). Outcomes worsen dramatically with larger core volumes (e.g., only 4.4% functional independence with cores ≥150mL in SELECT2).A critical complication is Malignant Cerebral Edema (MCE), affecting \~50% of large-core patients post-EVT. MCE triggers a vicious cycle of rising intracranial pressure, reduced perfusion, and brain herniation. It drastically worsens prognosis: functional independence rates plummet (13.3% vs 51.2% without MCE), mortality significantly increases (OR=7.96, p=0.001), and functional outcomes deteriorate (OR=7.83, p=0.008). Strong predictors include low ASPECTS (\<7) and large infarct volume.Decompressive Hemicraniectomy (DHC) is a life-saving intervention for MCE. Landmark trials (DESTINY, DECIMAL, HAMLET) and their meta-analysis show DHC within 24 hours in patients aged 18-60 significantly increases 12-month survival (78% vs 29%, ARR 50%) and rates of ambulatory independence (mRS ≤3: 43% vs 21%, ARR 23%). DESTINY II confirmed benefit in patients \>60, improving functional outcomes (mRS 0-4: 38% vs 16%). Guidelines endorse DHC for large infarcts with deterioration.However, significant challenges persist: DHC is Underutilized: Despite evidence, clinical adoption remains low.Rescue DHC Fails to Improve Outcomes in Post-EVT MCE: Studies report poor functional outcomes (only 20% mRS 0-2) and high mortality (48.6%) with standard medical therapy (SMT) plus rescue DHC after MCE develops. Retrospective data confirms worse outcomes in these patients (mRS 0-2: 16.4% vs 50%; mortality: 46.5% vs 20%) compared to those without MCE. Crucially, rescue DHC itself fails to improve prognosis once MCE is established (mRS 5-6: 64% vs 57.7%; mortality: 48% vs 46.2%).High-Risk Identification: Patients defined as high-risk for MCE (ASPECTS 3-5 + NIHSS≥30 or ASPECTS≤2) have significantly worse 90-day outcomes (mRS 0-2: 23.2% vs 44.6%; mortality: 44% vs 22.7%).Timing is Critical: Rescue DHC is often performed too late, after irreversible neurological damage occurs. Early/Prophylactic DHC, performed before significant edema and herniation develop, offers a potential pathophysiological advantage. It may:Improve cerebral perfusion pressure earlier. Reduce mass effect and edema progression. Mitigate secondary injury (e.g., reduce oxygen-free radicals, excitatory amino acids).Potentially break the ischemic-edema-herniation cycle sooner.Rationale for the Study: While DHC is effective for established MCE in non-EVT contexts and rescue DHC post-EVT is ineffective, high-quality evidence for early prophylactic DHC in high-risk large-core patients after successful EVT is lacking. Current guidelines do not address this specific, high-risk population where MCE incidence is \~50% and outcomes are dismal despite recanalization. Study Aim: This trial will evaluate the efficacy and safety of early prophylactic decompressive hemicraniectomy compared to standard medical treatment (which includes rescue DHC if MCE develops) in AIS-LVO patients at high risk of MCE (defined by ASPECTS and NIHSS criteria) following successful EVT. The goal is to determine if proactive intervention can improve functional outcomes and reduce mortality in this critically ill population where current strategies fail.
CONDITIONS
Official Title
Early Prophylactic Decompressive Hemicraniectomy Following Endovascular Therapy in Large Hemispheric Infarct Trial
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Premorbid modified Rankin Scale (mRS) score of 0 or 1
- Time from symptom onset to arterial puncture is 24 hours or less, including wake-up or unwitnessed strokes
- Age between 18 and 75 years
- Confirmed occlusion in the internal carotid artery (ICA) or middle cerebral artery (MCA)-M1 segment by imaging
- National Institutes of Health Stroke Scale (NIHSS) score with item 1a at least 1, excluding alertness changes due to cerebral edema
- Meeting either ASPECTS 3-5 with NIHSS 30 or higher, or ASPECTS 0-2
- Imaging signs of infarct affecting at least 50% of the middle cerebral artery territory
- No midline shift or midline shift less than 5 mm
- Successful mechanical thrombectomy with recanalization grade eTICI 2b50 or better
- Ability to start decompressive hemicraniectomy within 6 hours after thrombectomy and within 4 hours after randomization
- Informed consent obtained from patient or legal representative
You will not qualify if you...
- Signs or symptoms of brain herniation before randomization, such as unequal pupils or unstable vital signs
- Likely withdrawal of supportive care within the first day as judged by the investigator
- Planned decompressive hemicraniectomy before enrollment
- Severe, sustained high blood pressure (systolic >220 mm Hg or diastolic >110 mm Hg)
- Baseline blood glucose less than 50 mg/dl or greater than 400 mg/dl
- Baseline platelet count below 100 x10^9/L
- Known bleeding disorders, coagulation factor deficiencies, or use of anticoagulants with INR greater than 1.7
- Severe kidney failure defined by serum creatinine above 3.0 mg/dl or glomerular filtration rate below 30 ml/min, or need for dialysis
- Inability to complete 90-day follow-up due to lack of fixed residence or living overseas
- Suspected vasculitis or septic embolism
- Pre-existing neurological or mental disorders affecting condition assessment
- Pregnancy or lactation in females
- Participation in other clinical trials that may interfere with this study
- Life expectancy less than 3 months from non-stroke-related conditions or inability to comply with follow-up
- Other conditions deemed unsuitable or risky by investigators
- Evidence of other brain diseases such as trauma, tumors (except small meningioma), or aneurysms
- Acute ischemic infarction affecting both sides of the anterior circulation or posterior circulation (except fetal or near-fetal PCA)
- Vascular perforation during thrombectomy
- Pre-randomization imaging showing severe brain bleeding, diffuse subarachnoid hemorrhage, or intraventricular hemorrhage (mild localized bleeding without midline shift allowed)
AI-Screening
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Trial Site Locations
Total: 2 locations
1
Xuanwu Hospital, Capital Medical University.
Beijing, China
Not Yet Recruiting
2
Liaocheng Brain Hospital
Shandong, China
Actively Recruiting
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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