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Efficacy of a Minimally Invasive Therapy Adjuvant to the Standards of Care by Cyanoacrylate Embolization (LEADH)

Primary Purpose

Chronic Subdural Hematoma

Status
Recruiting
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
Medical treatment
Surgical treatment
embolization of the MMA
Sponsored by
University Hospital, Brest
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Chronic Subdural Hematoma focused on measuring Cyanoacrylate, Embolization, Middle meningeal artery, Recurrence of chronic subdural hematoma

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patient with a more than 10 mm CSH confirmed by NCCT
  • CSH localized to convexity
  • Patient aged 18 years or more at the time of the enrollment
  • Patient beneficiary from health insurance

Exclusion Criteria:

  • Any contraindication as required per angiogram procedure (severe renal failure, allergy…)
  • Pre-existing severe disability resulting in baseline mRS score > 4
  • Life expectancy of less than 6 months due to another cause than CSH
  • Patient under legal protection or deprived of liberty by a judicial or administrative decision
  • Pregnant or breastfeeding women

Sites / Locations

  • CHU Amiens-PicardieRecruiting
  • CHU Bordeaux
  • CHU BrestRecruiting
  • CHU CaenRecruiting
  • CHU NancyRecruiting
  • CHU Nantes
  • Hôpital Pitié Salpêtrière
  • CHU Tours
  • CHU Martinique

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Other

Other

Experimental

Experimental

Arm Label

Medical treatment alone

Surgical treatment alone

Medical treatment associated with an embolization of the MMA

Surgical treatment associated with an embolization of the MMA

Arm Description

Medical treatment without embolization of the MMA.

Surgical treatment without embolization of the MMA.

Medical treatment + embolization under local anesthesia or conscious sedation. The embolization will be carried out by femoral or radial arterial guided by pre-embolization cervical CTA. The middle meningeal artery will be catheterized then embolized by cyanoacrylates until the occlusion of the MMA.

Surgical treatment + embolization under local anesthesia or conscious sedation. The embolization will be carried out by femoral or radial arterial guided by pre-embolization cervical CTA. The middle meningeal artery will be catheterized then embolized by cyanoacrylates until the occlusion of the MMA.

Outcomes

Primary Outcome Measures

Number of CSH recurrence defined by the composite endpoint
CSH recurrence defined by the composite endpoint: A symptomatic CSH during the 6 month FU period A secondary surgical management during the 6 months FU period A remaining or reaccumulated hematoma on NCCT at 6 months

Secondary Outcome Measures

Number of symptomatic CSH during the FU period
Number of symptomatic CSH during the FU period
Number of secondary surgical management during the FU period
Number of secondary surgical management during the FU period
Number of remaining or reaccumulated hematoma on NCCT
Number of remaining or reaccumulated hematoma on NCCT
Clinical efficacy
Mortality rate
Clinical efficacy
Shift Modified Rankin Scale (mRS) (min = 0 = better outcome, max = 5 = worse outcome)
Clinical efficacy
Rapid Arterial oCclusion Exam (RACE) score evaluation (min = 0 = better outcome, max = 9 = worse outcome)
Clinical efficacy
Quality of life of patients will be evaluated by the EuroQol-5Dimensions-5L questionnaire
Clinical efficacy
Neurological exam : Barthel Scale (min = 0 = worse outcome, max = 100 = better outcome)
Success rate of the embolization (success = technical success of the procedure. Failure of the procedure = total or partial (catheterization, injection, other)).
Success rate of the embolization (success = technical success of the procedure. Failure of the procedure = total or partial (catheterization, injection, other)).
Complication rate of the embolization
Complication rate of the embolization
Volumetry of the CSH, calculated by the ABC/2 method.
Volumetry of the CSH, calculated by the ABC/2 method.
Maximum thickness of the CSH in mm.
Maximum thickness of the CSH in mm.
Comparison of the rate of AE in both groups
Comparison of the rate of AE in both groups
Comparison of the rate of SAE in both groups
Comparison of the rate of SAE in both groups

Full Information

First Posted
April 29, 2022
Last Updated
August 29, 2023
Sponsor
University Hospital, Brest
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1. Study Identification

Unique Protocol Identification Number
NCT05374681
Brief Title
Efficacy of a Minimally Invasive Therapy Adjuvant to the Standards of Care by Cyanoacrylate Embolization
Acronym
LEADH
Official Title
LEADH: Efficacy of a Minimally Invasive Therapy Adjuvant to the Standards of Care by Cyanoacrylate Embolization : Liquid Embolic Agent for the Treatment of Chronic subDural Hematoma a Randomized Control Study
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Recruiting
Study Start Date
March 28, 2023 (Actual)
Primary Completion Date
September 28, 2026 (Anticipated)
Study Completion Date
September 28, 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Brest

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Chronic subdural hematomas (CSH) are collections of blood in the subdural space. CSH are becoming the most common cranial neurosurgical condition among adults, and a significant public health problem, due to an increasing use of anticoagulant and antiplatelet medication in an ageing population. Symptomatic CSH, or CSH with a significant mass effect, are treated surgically. However, recurrences are common (10 to 20%). Conservative management (medical) is used in patients who are asymptomatic or have minor symptoms. However, therapeutic failures, requiring surgical treatment, are common. The pathophysiology of CSH involves inflammation, angiogenesis, and clotting dysfunction. Self-perpetuation and rebleeding is thought to be caused by neo-membranes from the inflammatory remodeling of the dura-mater mainly fed by the distal branches of the middle meningeal artery (MMA). There are 13 ongoing registered RCTs in CSH, with the most common covering application of steroids, surgical techniques and tranexamic acid. Further to this, there are trials running on other pharmacological agents, and peri-operative management. Some industrial or academic trials are or will enroll in France in the next year in France. But to our best knowledge, none of these trials will the eventual benefits of the MMA embolization in both cases of medical and/or surgical management, and none will focus on the use of cyanoacrylates (CYA) for this purpose. Preliminary case series and nonrandomized retrospective studies have suggested that MMA embolization alone or as adjuvant therapy to surgery can decrease recurrences. The investigators hypothesize that in both conditions of conservative or surgical managements, endovascular embolization of patients with CSH significantly reduces the risk of recurrence of CSH. The investigators choose the CYA as liquid embolic agent because of the pain and cost of the use of Ethylen Vinyl alcohol copolymer (EVOH) agents and its simplicity to be used.
Detailed Description
Indication of surgical or conservative management will be decided by the neurosurgeon. Experimental arm: CSH requiring hematoma removal will be surgically managed with a surgical technique applied depending on the surgeon's discretion. Medical management will be adopted according to neurosurgeons habits. MMA embolization (on the CSH side or bilaterally if necessary) in the Experimental Arms will be performed with Cyanoacrylates and preferentially using conscious sedation or local anesthesia. • Control arm: CSH requiring hematoma removal will be surgically managed with a surgical technique applied depending on the surgeon's discretion. Medical management will be adopted according to neurosurgeons habits • Primary and secondary end points will be assessed at 2 months+/- 1 month and assessed at 6 +/- 2 months. The blind items will be the mRS and the RACE score. The volume of the CSH will be semi-automatically assessed using the ABC/2 method and the estimated maximal thickness of the CSH on axial images.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Subdural Hematoma
Keywords
Cyanoacrylate, Embolization, Middle meningeal artery, Recurrence of chronic subdural hematoma

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
550 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Medical treatment alone
Arm Type
Other
Arm Description
Medical treatment without embolization of the MMA.
Arm Title
Surgical treatment alone
Arm Type
Other
Arm Description
Surgical treatment without embolization of the MMA.
Arm Title
Medical treatment associated with an embolization of the MMA
Arm Type
Experimental
Arm Description
Medical treatment + embolization under local anesthesia or conscious sedation. The embolization will be carried out by femoral or radial arterial guided by pre-embolization cervical CTA. The middle meningeal artery will be catheterized then embolized by cyanoacrylates until the occlusion of the MMA.
Arm Title
Surgical treatment associated with an embolization of the MMA
Arm Type
Experimental
Arm Description
Surgical treatment + embolization under local anesthesia or conscious sedation. The embolization will be carried out by femoral or radial arterial guided by pre-embolization cervical CTA. The middle meningeal artery will be catheterized then embolized by cyanoacrylates until the occlusion of the MMA.
Intervention Type
Other
Intervention Name(s)
Medical treatment
Intervention Description
Medical treatment alone
Intervention Type
Other
Intervention Name(s)
Surgical treatment
Intervention Description
Surgical treatment alone
Intervention Type
Other
Intervention Name(s)
embolization of the MMA
Intervention Description
The middle meningeal artery will be catheterized then embolized by cyanoacrylates until the occlusion of the MMA.
Primary Outcome Measure Information:
Title
Number of CSH recurrence defined by the composite endpoint
Description
CSH recurrence defined by the composite endpoint: A symptomatic CSH during the 6 month FU period A secondary surgical management during the 6 months FU period A remaining or reaccumulated hematoma on NCCT at 6 months
Time Frame
At 6 month
Secondary Outcome Measure Information:
Title
Number of symptomatic CSH during the FU period
Description
Number of symptomatic CSH during the FU period
Time Frame
At 6 month
Title
Number of secondary surgical management during the FU period
Description
Number of secondary surgical management during the FU period
Time Frame
At 6 month
Title
Number of remaining or reaccumulated hematoma on NCCT
Description
Number of remaining or reaccumulated hematoma on NCCT
Time Frame
At 6 month
Title
Clinical efficacy
Description
Mortality rate
Time Frame
At 6 month
Title
Clinical efficacy
Description
Shift Modified Rankin Scale (mRS) (min = 0 = better outcome, max = 5 = worse outcome)
Time Frame
At 6 month
Title
Clinical efficacy
Description
Rapid Arterial oCclusion Exam (RACE) score evaluation (min = 0 = better outcome, max = 9 = worse outcome)
Time Frame
At 6 month
Title
Clinical efficacy
Description
Quality of life of patients will be evaluated by the EuroQol-5Dimensions-5L questionnaire
Time Frame
At 6 month
Title
Clinical efficacy
Description
Neurological exam : Barthel Scale (min = 0 = worse outcome, max = 100 = better outcome)
Time Frame
At 6 month
Title
Success rate of the embolization (success = technical success of the procedure. Failure of the procedure = total or partial (catheterization, injection, other)).
Description
Success rate of the embolization (success = technical success of the procedure. Failure of the procedure = total or partial (catheterization, injection, other)).
Time Frame
At 6 month
Title
Complication rate of the embolization
Description
Complication rate of the embolization
Time Frame
At 6 month
Title
Volumetry of the CSH, calculated by the ABC/2 method.
Description
Volumetry of the CSH, calculated by the ABC/2 method.
Time Frame
At 6 month
Title
Maximum thickness of the CSH in mm.
Description
Maximum thickness of the CSH in mm.
Time Frame
At 6 month
Title
Comparison of the rate of AE in both groups
Description
Comparison of the rate of AE in both groups
Time Frame
At 6 month
Title
Comparison of the rate of SAE in both groups
Description
Comparison of the rate of SAE in both groups
Time Frame
At 6 month

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patient with a more than 10 mm CSH confirmed by NCCT CSH localized to convexity Patient aged 18 years or more at the time of the enrollment Patient beneficiary from health insurance Exclusion Criteria: Any contraindication as required per angiogram procedure (severe renal failure, allergy…) Pre-existing severe disability resulting in baseline mRS score > 3 Life expectancy of less than 6 months due to another cause than CSH Patient under legal protection or deprived of liberty by a judicial or administrative decision Pregnant or breastfeeding women
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
jean-Christophe GENTRIC, PhD
Phone
0298347520
Email
jean-christophe.gentric@chu-brest.fr
Facility Information:
Facility Name
CHU Amiens-Picardie
City
Amiens
ZIP/Postal Code
80054
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Cyril CHIVOT, Dr
Email
chivot.cyril@chu-amiens.fr
First Name & Middle Initial & Last Name & Degree
Cyril CHIVOT, Dr
Facility Name
CHU Bordeaux
City
Bordeaux
ZIP/Postal Code
33076
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Gaultier MARNAT, Dr
Email
gaultier.marnat@chu-bordeaux.fr
First Name & Middle Initial & Last Name & Degree
Gaultier MARNAT, Dr
Facility Name
CHU Brest
City
Brest
ZIP/Postal Code
29609
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jean-Christophe GENTRIC, PhD
Email
jean-christophe.gentric@chu-brest.fr
First Name & Middle Initial & Last Name & Degree
Jean-Christophe GENTRIC, PhD
Facility Name
CHU Caen
City
Caen
ZIP/Postal Code
14000
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Charlotte BARBIER, Dr
Email
barbier-c@chu-caen.fr
First Name & Middle Initial & Last Name & Degree
Charlotte BARBIER, Dr
Facility Name
CHU Nancy
City
Nancy
ZIP/Postal Code
54035
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Benjamin GORY, Pr
Email
B.GORY@chru-nancy.fr
First Name & Middle Initial & Last Name & Degree
Benjamin GORY, Pr
Facility Name
CHU Nantes
City
Nantes
ZIP/Postal Code
44000
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Romain BOURCIER, Dr
Email
romain.bourcier@chu-nantes.fr
First Name & Middle Initial & Last Name & Degree
Romain BOURCIER, Dr
Facility Name
Hôpital Pitié Salpêtrière
City
Paris
ZIP/Postal Code
75013
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Frédéric CLARENCON, Pr
Email
frederic.clarencon@aphp.fr
First Name & Middle Initial & Last Name & Degree
Frédéric CLARENCON, Pr
Facility Name
CHU Tours
City
Tours
ZIP/Postal Code
37000
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Grégoire BOULOUIS, Dr
First Name & Middle Initial & Last Name & Degree
Grégoire BOULOUIS, Dr
Facility Name
CHU Martinique
City
Fort-de-France
ZIP/Postal Code
97261
Country
Martinique
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Célia TUTTLE, Dr
First Name & Middle Initial & Last Name & Degree
Célia TUTTLE, Dr

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
All collected data that underlie results in a publication
IPD Sharing Time Frame
Data will be available beginning three years and ending fifteen years following the final study report completion.
IPD Sharing Access Criteria
Data access requests will be reviewed by the internal committee of Brest UH. Requestors will be required to sign and complete a data access agreement.

Learn more about this trial

Efficacy of a Minimally Invasive Therapy Adjuvant to the Standards of Care by Cyanoacrylate Embolization

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