Clinical trial Recruiting at 1 site Interventional Ages 18 and up

Middle Meningeal Artery Coagulation During Burr-Hole Drainage for Chronic Subdural Haematoma

Official title: BURR-MMA: A Prospective Pilot Feasibility Study of Intra-operative Middle Meningeal Artery Coagulation During Burr-Hole Surgery for Chronic Subdural Haematoma

Run by University College, London · NCT07549893 · Data updated 2026-11-12

This study tests whether safely coagulating small branches of the middle meningeal artery during burr-hole drainage can reduce recurrence of chronic subdural haematoma in adults receiving standard surgical care.

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment30 (estimated)
SponsorUniversity College, London
Academic / other
Drugs / interventionsradiation
Locations1 site (London)
StatusRecruiting
StartedAugust 1, 2026
Main results expectedJuly 1, 2027
Study endsDecember 1, 2027
Registry record updatedAugust 4, 2026
Trial IDNCT07549893 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults aged 18 years or older undergoing burr-hole drainage for chronic or subacute subdural hematoma, where the surgeon considers the MMA adjunct feasible and safe to attempt.

Probably not a fit

Patients in whom the MMA adjunct is not technically feasible or who experience intraoperative bail-out will not receive the adjunct benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This is a single-centre feasibility study evaluating a workflow-integrated technique to partially coagulate distal branches of the middle meningeal artery during routine burr-hole drainage for chronic or subacute subdural hematoma. Using pre-operative CT mapping and neuronavigation, surgeons perform limited bipolar coagulation of MMA branches through the planned burr-hole, without extra imaging or implants. The primary aims are technical deliverability, safety, and fidelity of the procedure, with Day 90 follow-up and exploratory outcomes to inform design for a future multicentre study. All imaging is part of routine care, and no additional radiation is introduced for study participation. The trial is IDEAL Stage 2a, single-arm, enrolling 20-30 adults.

Why it matters

Potential benefit: If successful, this approach could lower recurrence rates after burr-hole drainage by targeting the blood supply to the outer membrane of the hematoma.

How similar studies have gone: Endovascular MMA embolisation has shown recurrence reduction, but this study tests a different in-workflow, intraoperative coagulation approach that is less invasive than embolisation.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Age ≥18 years.
* Chronic or subacute subdural haematoma scheduled for burr-hole evacuation.
* Treating surgeon considers the CT- and navigation-guided MMA adjunct technically feasible and safe to attempt, recognising that the adjunct may be abandoned intra-operatively according to protocol bail-out criteria.
* Written informed consent, or consultee declaration under the Mental Capacity Act (MCA), with re-consent if capacity returns.

Consented participants who meet eligibility criteria will be enrolled sequentially until the target sample size of 20-30 participants is reached. No randomisation is used in this feasibility phase.

Exclusion Criteria:

* Acute subdural haematoma requiring craniotomy or decompressive surgery.
* Prior ipsilateral MMA embolisation.
* Clear contraindication to pre-operative CT
* Inability to complete Day-90 follow-up.
* Pregnancy or breastfeeding (due to radiation exposure from CT imaging as part of standard clinical care).

If CT is non-diagnostic or cannot be performed, participants will continue with standard burr-hole evacuation without the MMA adjunct; this does not constitute a protocol deviation.

Where it's running

  • National Hospital for Neurology and Neurosurgery
    London, United Kingdom
    Recruiting

Study contacts

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.