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NCT Number: NCT06466733

Puerto Rico Embolization of the Middle Meningeal Artery for the Treatment of Chronic Subdural Hematoma Trial (PREMMA)

Puerto Rico Embolization of the Middle Meningeal Artery (PREMMA) trial is a multi-center, parallel, prospective, superiority, randomized controlled trial with concealed allocation comparing reoperation rates and neurological outcomes in patients with chronic subdural hematoma that receive treatment via embolization of the middle meningeal artery versus surgical evacuation via burr hole trephination or craniotomy.

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Key information

About this study

Chronic subdural hematoma (cSDH) is a collection of fluid and blood breakdown products that evolves over weeks to months in the subdural space. This condition is more common among people older than 65 years and has been associated with increased use of antithrombotic therapy among this population. The World population is rapidly aging; thus, the investigators expect the number of patients with cSDH will increase. The United Nations World Social Report places Puerto Rico in the 7th place of countries with the largest share of people aged 65 years or over. This pathology burdens healthcare systems; therefore, assessing the feasibility of treatment modalities for cSDH that are less invasive, have lower procedural risks, and have lower recurrence rates that require additional surgical intervention is essential.

The standard of care for symptomatic cSDH is the surgical evacuation (SE) of the hematoma, with recurrence rates between 10-30% and surgical rescue indicated for most of these cases. Evacuation of the hematoma effectively relieves its mass effect but does not change the underlying pathophysiologic mechanism. In recent years, embolization of the middle meningeal artery (eMMA) has been shown to decrease the recurrence of chronic subdural hematoma and the need for revision burr hole or craniotomy. The PREMMA trial aims to compare embolization of the middle meningeal artery as stand-alone treatment for chronic subdural hematoma versus the standard of care, surgical evacuation.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age ≥ 21
  • Speak and understand Spanish or English
  • Resident of Puerto Rico
  • Glasgow coma scale ≥ 14/15
  • Presence of cSDH on non-contrast computed tomography (NCCT) or magnetic resonance imaging (MRI)
  • Neurological indication for treatment of cSDH (Markwalder scale ≤ 2)
  • No previous surgical or endovascular treatment for symptomatic cSDH
  • Signed informed consent for participation in the study by the patient or legally authorized representative

Exclusion criteria

  • Acute subdural hematoma
  • Focal, non-hemispheric localization of cSDH
  • Evidence of other lesions associated with cSDH, such as neoplasms, vascular lesions, or additional epidural, subarachnoid, or parenchymal hemorrhage on non-contrast computed tomography or magnetic resonance imaging
  • Imaging evidence of skull fracture over the subdural hematoma
  • Presence of any cerebrospinal fluid (CSF) shunt
  • Imaging evidence of midline shift ≥ 10 mm
  • Imaging evidence of basal cistern effacement
  • Imaging evidence of dilatation of lateral ventricles
  • Imaging evidence of uncal herniation
  • Modified Rankin scale ≥ 3 before developing symptoms associated with cSDH
  • Contraindications for angiography (i.e., complex anatomy or kidney failure)
  • Comorbidity making follow-up impossible
  • Pregnancy
  • Vulnerable patients, including homeless patients, incarcerated patients, and mentally ill patients without appropriate medical decision-making proxies that the physician believes are incapable of appropriately assessing the risks of the procedure
  • Absence of medical insurance

Treatment and study plan

Embolization of the middle meningeal artery

Procedure

Embolization of the middle meningeal artery ipsilateral to the chronic subdural hematoma is performed infusing embolic polyvinyl alcohol (PVA) microparticles.

Surgical Evacuation via burr hole or craniotomy

Procedure

The standard of care for chronic subdural hematoma, burr hole or craniotomy are performed ipsilateral to the lesion.

Other names: Burr hole, Craniotomy

Primary outcomes

  1. Reoperation

    Time frame: 3 months, 6 months, and 12 months

    Number of patients requiring reoperation due to recurrent chronic subdural hematoma.

Secondary outcomes

  1. Modified Rankin Scale (mRS)

    Time frame: Pre-operative, 24 hours, 2 weeks, 1.5 months, 3 months, 6 months, and 12 months

    The modified Rankin Scale (mRS) will assess neurological disability. The scale comprises seven levels, from 0 to 6, with higher scores indicating greater disability, and 6 indicating death.

  2. Glasgow Coma Scale (GCS)

    Time frame: Pre-operative, 24 hours, 2 weeks

    The Glasgow coma scale (GCS) will assess consciousness level. GCS score can range from 3 (completely unresponsive) to 15 (completely alert and oriented).

  3. Visual Analog Scale (VAS)

    Time frame: Pre-operative, 24 hours, 2 weeks, 1.5 months, 3 months, 6 months, 12 months

    The visual analog scale (VAS) will assess pain levels. VAS represents the severity of pain from 0 "no pain" to 10 "very severe pain."

  4. Quality of life (EQ-5D-5L)

    Time frame: Pre-operative, 2 weeks, 1.5 months, 3 months, 6 months, 12 months

    Will be measured with the EuroQol 5 dimensions and 5 levels (EQ-5D-5L) grading scale.

  5. Radiological outcomes

    Time frame: Pre-operative, 24 hours, 3 months, 6 months, 12 months

    Will be measured by routine computed tomography compared with pre-operative images.

  6. Technical success of embolization of the middle meningeal artery (eMMA)

    Time frame: 24 hours

    The rate of unsuccessful eMMA due to technical failure or anatomical issues will be recorded.

  7. Procedure-related complications

    Time frame: 24 hours, 2 weeks, 1.5 months, 3 months

    Any life-threatening event from enrollment to discharge will be recorded.

  8. Adverse events

    Time frame: 24 hours, 2 weeks, 1.5 months, 3 months

    Any unintentional injury or complication involving a prolonged stay, disability at discharge, or death caused by healthcare management, not the underlying disease, will be recorded.

  9. Post-operative morbidity

    Time frame: 24 hours, 2 weeks, 1.5 months, 3 months

    All surgical and/or medical complications that occur.

  10. Mortality

    Time frame: 24 hours, 2 weeks, 30 days, 1.5 months, 3 months, 6 months, 12 months

    The number of participants among the total number of deaths.

  11. Length of stay

    Time frame: From date of randomization until the date of discharge or date of death from any cause while patient is in hospital, whichever came first, assessed up to 90 days

    The patient's hospitalization period.

Study contacts

Contact information is provided by the study sponsor or research team.

Maria M Garcia Perez

CONTACT

[email protected]

939-417-4432

Sponsors and collaborators

Lead sponsor

Juan M. Ramos Acevedo

Other

Registry information

Acronym: PREMMA

Important dates

Study start
2025
Primary completion
2031
Study completion
2032
First posted
Jun 20, 2024
Registry last updated
May 7, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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