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Preventing Recurrences of Chronic Subdural Hematoma in Adult Patients by Middle Meningeal Artery Embolization

Middle Meningeal Artery Embolization Minimizes Burdensome Recurrence Rates After Newly Diagnosed Chronic Subdural Hematoma Evacuation (MEMBRANE)

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05327933
Acronym
MEMBRANE
Enrollment
154
Registered
2022-04-14
Start date
2022-05-26
Completion date
2025-10-31
Last updated
2025-03-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hematoma, Subdural, Chronic

Brief summary

Patients with a chronic subdural hematoma (cSDH), that is, a blood accumulation between two meninges developing over a long period of time, often have recurrent bleedings after an initial operation. The study aims to show that additional surgery reduces the risk of recurrent bleeding. The additional procedure aims to block small blood vessels in the skull with tiny plastic particles. The small blood vessels are embolized using X-rays and a contrast medium and a fine tube that is inserted into the diseased vessels of the head via the groin. Patients of full age who have undergone burr hole trepanation as a first operation, i.e. a blood drain through a hole in the cranial cavity, can participate in the study. Participating patients are randomly assigned to a control group with treatment according to clinical routine or a treatment group with an additional occlusion of the blood vessels in the skull. In addition, patients can consent to a genetic test to determine the relationship between a coagulation factor and the risk of recurrence of the hematoma. In order to record the test results, check-up examinations are carried out after one and three months.

Interventions

PROCEDURESurgery plus endovascular MMA embolization

A micro catheter is inserted transfemorally into the branches of the middle meningeal artery (MMA) in a minimally invasive manner and the periphery is occluded using polyvinyl alcohol (PVA) particles to prevent future bleeding. If the desired catheter position cannot be achieved due to the anatomical conditions, a more proximal closure of the MMA using Onyx® or micro-electric coils is performed. Embolization of the MMA by PVA particles with sizes between 40-300 µm is preferred over embolization by coils and Onyx®, since the capillary network of the dura is entirely blocked when using particles. In order to identify the vessels to be closed, a digital subtraction angiography (DSA) is performed.

PROCEDURESurgery alone

Evacuation of cSDH

Sponsors

Unfallkrankenhaus Berlin
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Patients who have undergone surgery by means of one or more burr hole trepanations during the first manifestation of a cSDH (unihemispherical or bihemispherical) detected by computed tomography or magnetic resonance tomography 2. Age ≥18 years 3. Sufficient compliance and ability to consent 4. Patient's informed consent for surgical as well as endovascular interventional procedure and participation in the study

Exclusion criteria

1. Conservatively treated cSDH 2. Radiological evidence of an acute or subacute subdural hematoma, subarachnoid hemorrhage, intracerebral hematoma or epidural hematoma 3. Surgical technique: craniotomy, craniectomy, bilateral burr hole trepanation 4. Angiography cannot be performed within 72 hours after surgery 5. Age \<18 years 6. Supervisory relationship 7. Pregnancy 8. Lack of informed consent 9. Lack of compliance 10. Homozygous factor XIII deficiency with residual activity \<10%

Design outcomes

Primary

MeasureTime frameDescription
cSDH recurrence rates after surgeryWithin three months of follow-upA recurrence occurs when at least one of the following criteria is met: * recurrent cSDH with at least the same volume (\>- 10%) compared to the findings at baseline and / or * recurrent cSDH which requires surgery

Secondary

MeasureTime frameDescription
Impairment due to neurological deficits assessed by the modified Rankin ScaleEvaluated at three months after baselineModified Rankin scale ranges from 0 (no symptoms) to 5 (severe disability)
Number of recurrence-associated complicationsWithin three months of follow-upExamined on a binary scale
Number of complications associated with interventional therapyWithin three months of follow-upExamined on a binary scale

Other

MeasureTime frameDescription
Relationship between factor XIII deficiency and risk of recurrenceWithin three months of follow-upFactor XIII deficiency is defined if the factor XIII concentration at baseline and/or the factor XIII activity after cryopreservation is \<70%.
Predisposition of the genetic variants F13A1 rs2815822 and F13B rs12134960 for factor XIII deficiencyWithin three months of follow-upThe existence of genetic variants F13A1 rs2815822 or F13B rs12134960 in the blood of the subjects is determined on a binary scale.

Countries

Germany

Contacts

Primary ContactJohannes Lemcke, PD Dr. med.
johannes.lemcke@ukb.de00493056813701
Backup ContactLeonie Goelz, Dr. med.
leonie.goelz@ukb.de

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 14, 2026