SQUID Embolization
DeviceEmbolization of the Middle Meningeal Artery using the SQUID non-adhesive liquid embolic agent
NCT Number: NCT04410146
STEM Study is a pivotal, international, multi-center, prospective, randomized (1:1) controlled trial designed to provide an assessment of the safety and effectiveness of Middle Meningeal Artery (MMA) embolization with SQUID for the management of Chronic Subdural Hematoma (cSDH)
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Notify Me30 year and older
All sexes
Interventional
Not applicable
Chu Cote de Nacre, Caen, France
The study objective is to provide an assessment of the safety and effectiveness of Middle Meningeal Artery (MMA) embolization with SQUID for the management of Chronic Subdural Hematoma (cSDH).
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Embolization of the Middle Meningeal Artery using the SQUID non-adhesive liquid embolic agent
Embolization of the Middle Meningeal Artery using the SQUID non-adhesive liquid embolic agent and the surgical of the sub-dural hematoma
Surgical evacuation of the sub-dural hematoma
Standard Medical Management
Time frame: On 180-day from intervention
Treatment failure as defined by the occurrence of any of the following events:
Time frame: Within 30-days from intervention
Major disabling stroke or any death within 30-days from intervention.
Time frame: Through 1-year visit
Number of participants with an adverse event (AE) or serious adverse event (SAE) adjudicated as probably or causally related to the investigational device or Middle Meningeal Artery Embolization (MMAE) procedure.
Time frame: 180-day from intervention
The modified Rankin Scale (mRS) is an ordinal scale used to measure the degree of disability or dependence in the daily activities of people who have suffered a stroke. Scores range from 0 (no symptoms) to 6 (death):
0: No symptoms
Time frame: 180 days
The Modified Rankin Scale (mRS) is a clinician-reported measure used to assess the degree of functional disability or dependence in daily activities following a neurological event. This binary outcome dichotomizes the 7-point scale (0-6) into two categories: Favorable Outcome (mRS 0-2) and Unfavorable Outcome (mRS 3-6).
A score of ≤ 2 signifies that the participant is functionally independent and capable of looking after their own affairs without assistance. Results will be reported as the proportion of participants in each treatment arm achieving a score of 0, 1, or 2 at the 180-day follow-up.
Time frame: Baseline and 180 Days
T-scores were used to convert raw data to standardized scale with a mean of 50 and a standard deviation of 10. A higher T-score indicates better cognitive performance (a score near 40 indicates a low average to average range). Global neurocognitive performance was assessed by taking the mean T-score for all individual neurocognitive markers (Hopkins Verbal Learning Tests (HVLT-R), Controlled Oral Word Association Test (COWAT), Animal Naming, and Trail making tests).
Time frame: 180-day change from Baseline
The EQ VAS is a 20 cm vertical visual analogue scale that records the patient's self-rated health today. It ranges from 0 (Worst health you can imagine) to 100 (Best health you can imagine).
Time frame: 180 day change from Baseline
The EQ-5D-5L (EuroQol - 5 Dimension - 5 Level) is a standardized, patient-reported instrument used globally to measure health-related quality of life (HRQoL). It assesses health across 5 dimensions-mobility, self-care, usual activities, pain/discomfort, and anxiety/depression-with 5 levels of severity. The index score ranges from -0.59 to 1.0, where 1.0 represents 'full health' and 0.0 represents death. A higher score indicates a better health-related quality of life. Change is calculated as (180-Day score minus Baseline score)
Time frame: Through 180 days
The number of days (mean) in hospital from baseline through 180 days.
Time frame: 90-day Change from Baseline
The National Institutes of Health Stroke Scale (NIHSS) is a standardized tool used to objectively quantify the neurological impairment caused by a stroke. It consists of 15 items assessing areas such as level of consciousness, vision, motor function, sensation, and language.
Score Range: Total scores range from 0 to 42. Interpretation: A score of 0 indicates normal function (no symptoms), while higher scores indicate more severe neurological deficit.
This outcome measures the mean change in the total NIHSS score from baseline (at enrollment) to the 90-day follow-up
Time frame: 180 days
The total number of ICU days from baseline through 180 days.
Time frame: 180 days Change from Baseline
Core Lab Analysis of CT/MRI Images. The thickness of the cSDH was documented separately for the left and right sides.
Balt USA
Industry
Acronym: STEM
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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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