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Middle Meningeal Artery Embolization for Patients with Chronic Subdural Hematoma

Not Applicable
Active, not recruiting
Conditions
Endovascular Treatment
Chronic Subdural Hematoma
Registration Number
NCT06772740
Lead Sponsor
Kazutaka Uchida
Brief Summary

COMPLEMENT study (ChrOnic subdural hematoMa Patients suppLemented with Embolization of Middle mENingeal artery Trial) is a prospective, open label, blinded endpoint (PROBE), Japanese, two-arm, randomized, controlled, post-market study to assess the efficacy and safety of middle meningeal artery embolization for chronic subdural hematoma.

Detailed Description

Not available

Recruitment & Eligibility

Status
ACTIVE_NOT_RECRUITING
Sex
All
Target Recruitment
600
Inclusion Criteria
  1. Age >=18
  2. pre-mRS 0-3
  3. Hematoma thickness >=10mm
  4. Having at least one risk factor Risk factor: Age >=75, Antithrombotic therapy, DM, Bilateral hematoma, Markwalder grading score >3, Preoperative volume >=130ml, Preoperative midline shift >=8mm, CT appearance (Homogeneous, laminar or separated)
Exclusion Criteria
  1. Cr >=1.8
  2. Plt <50,000, PT-INR >2
  3. Life expectancy <6 months

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Rate of recurrence of chronic subdural hematoma6 months after randomization

Recurrence of chronic subdural hematoma is defined as the maximum thickness of subdural hematoma exceeding 10 mm or the patient receiving re-operation.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Hyogo Medical University

🇯🇵

Nishinomiya, Hyogo, Japan

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