Skip to content

Efficacy and Safety of Preoperative Middle Meningeal Artery Embolization Before Craniotomy in Preventing the Expansion of Contralateral Epidural Hematoma in Acute Traumatic Brain Injury: A Prospective Single-Arm Exploratory Study

Efficacy and Safety of Preoperative Middle Meningeal Artery Embolization Before Craniotomy in Preventing the Expansion of Contralateral Epidural Hematoma in Acute Traumatic Brain Injury: A Prospective Single-Arm Exploratory Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600128001
Enrollment
Unknown
Registered
2026-07-13
Start date
2026-07-13
Completion date
Unknown
Last updated
2026-07-20

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

Conditions

Acute severe traumatic brain injury with high risk factors for contralateral epidural hematoma expansion

Interventions

Experimental group:Prophylactic contralateral middle meningeal artery embolization followed by ipsilateral craniotomy for hematoma evacuation and/or decompressive craniectomy.

Sponsors

Northern Jiangsu People's Hospital, Jiangsu Province, China
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Age range: 18 to 80 years old, gender not restricted; 2. History of closed head trauma, with the time from injury to admission 5 mm, etc.; 4. The contralateral side of the head has a small epidural hematoma (less than 20 ml) confirmed by the first head CT scan, or there is a temporal-parietal skull fracture crossing the middle meningeal artery groove; 5. GCS score at admission: 3 - 8; 6. Family members or legal representatives have signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1. There is clear primary brainstem injury or the expected survival period is less than 24 hours; 2. Both sides have reached the surgical indications that require immediate craniotomy before the operation; 3. Severe coagulation dysfunction, such as platelet count < 50×10^9/L and unable to be corrected within a short period of time; 4. There are contraindications for cerebral angiography or embolization, such as severe allergy to contrast agent; 5. Pregnant or lactating women.

Design outcomes

Primary

MeasureTime frame
Incidence of decompressive contralateral epidural hematoma expansion resulting in severe brain swelling or rescue surgery during surgery or within 72 hours after surgery;

Countries

China

Contacts

Public ContactXingdong Wang

Northern Jiangsu People's Hospital, Jiangsu Province, China

wangxingdong2013@163.com+86 514 8737 3563

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jul 23, 2026