Endovascular Coiling Using Target Tetra® Coils for Small Intracranial Aneurysm

Intracranial Aneurysm Clinical Trial

Official title:

Safety and Efficacy of Endovascular Coiling Using Target Tetra® Coils for Small Intracranial Aneurysm: Prospective, Open-label, Single Arm, Single Center Study

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT06064435
• Other study ID #: 1-2023-0053
• Status: Not yet recruiting
• Start date: December 2023
• Est. completion date: March 2026

Study information

• Verified date: December 2023
• Source: Yonsei University
• Contact: Keunyoung PARK, M.D.PhD.
• Phone: +82-2-2228-2150
• Email: kypark78.md[@]gmail.com
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

The goal of this study was to verify the safety and effectiveness of Target Tetra® Detachable Coil in the endovascular embolization treatment of small intracranial aneurysm (≤5mm).

Description:

The study is a Prospective Single-arm Single-center Registry that aims to assess the safety and efficacy of the Target Tetra Coils in the endovascular treatment of small intracranial aneurysms (≤5mm). The study is not designed as intervention or treatment study. The investigators will enroll up to 100 participants at the single center.

• Enrollment of patients: The following process is carried out for patients who have consented to participate in the study among non-ruptured or ruptured cerebral aneurysm patients selected based on the inclusion and exclusion criteria.
• Before the procedure, the following items are verified:
• Informed consent form
• Demographic information
• Past medical history and family history
• Vital signs
• Electrocardiogram (ECG) results (results from within the previous 12 weeks before the screening visit can be used)
• Laboratory test results (results from within the previous 12 weeks before the screening visit can be used): WBC, RBC, Hb, Hct, platelet count, PT INR, aPTT, cholesterol, ALP, AST, ALT, albumin, total bilirubin, total protein, BUN, creatinine, eGFR*, Urine-HCG†, FBS, triglycerides, LDL, PRU (VerifyNow test), and ARU (VerifyNow test) *eGFR = (140 - age) x (weight/72) x Creatinine
• Pregnancy test (if applicable)
• Imaging findings (results from within the previous 1 year before the screening visit can be used)
• Adverse events
• Concomitant medications/therapies
• Pre-procedure modified Rankin Scale (mRS) assessment ③ Following the established method, coil embolization is performed under general anesthesia, and mechanical or technical failures of the Target Tetra® Detachable Coil occurring during the treatment are investigated.
• Failure to advance or insert
• Stretch
• Disconnection
• Detachment failure
• Material deformation
• Difficult to remove
• Peeled or delaminated device
• Premature detachment ④ During the procedure and within 30 days post-procedure, neurological and non-neurological complications are investigated.
• Neurological complications -Any cause of death
• Any intracranial thromboembolism (asymptomatic or symptomatic)
• Any intracranial hemorrhage including aneurysm perforation
• Any intracranial vessel injury
• Miscellaneous: any ocular hemorrhage
• Non-neurological complications -Puncture site complication requiring any intervention -Pseudoaneurysm -Arteriovenous (AV) fistula -Hematoma requiring transfusion -Retroperitoneal hemorrhage -Arterial dissection
• Thromboembolism including limb ischemia
• Miscellaneous: infection, vessel rupture/perforation
• Complications related to general anesthesia
• After the procedure, the occlusion rate of cerebral aneurysms (modified Raymond Scale; complete occlusion, neck remnant, sac remnant) and packing density are evaluated.
• Modified Raymond Scale
• Packing Density Packing Density = Volume of coils placed in the aneurysm / Volume of the aneurysm measured on a 3D workstation (%) The above process is conducted through the open-source Angiosuite application. ⑥ Characteristics of cerebral aneurysms in patients who have been treated with Target Tetra® Detachable Coils in over 70% of the total packing density are identified. ⑦ Clinical outcomes (mRS) are evaluated at 1 month, 6 months, 12 months of follow-up.

⑧ At 6 months, 12 months, the occlusion rate of cerebral aneurysms (Modified Raymond Scale) and recurrence are assessed by at least two neurosurgery specialists using 3T-MR angiography or cerebral angiography. ⑨ Patients who have not been treated with Target Tetra® Detachable Coils in over 70% of the total packing density are excluded from the analysis. The independent Study Monitoring will be regularly proceed and processed on the basis of the permission of instituitional review board.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 100
• Est. completion date: March 2026
• Est. primary completion date: March 2026
• Gender: All
• Age group: 19 Years to 80 Years

Eligibility

Inclusion Criteria:

1. Adults aged 19 to 80 years

2. Patients with intracranial aneurysms suitable for endovascular embolization therapy with a maximum diameter of 5mm or less

3. Including both ruptured and unruptured intracranial aneurysms

4. Patients for whom the use of Target Tetra® coil is expected in endovascular coil embolization therapy

5. Patients who have undergone balloon-assisted coiling or adjunctive stent placement during coil embolization

6. Subjects who have received an explanation of the clinical study and provided written consent to participate in the study

Exclusion Criteria:

1. Age below 18 or above 81 years

2. Infectious, dissecting, traumatic, or mycotic aneurysms

3. Patients who have undergone surgical or endovascular treatment for the target intracranial aneurysm

4. Patients in whom vascular access to the target intracranial aneurysm is not possible due to conditions such as moyamoya disease, dural arteriovenous malformation, significant atherosclerotic stenosis, or severe vessel tortuosity

5. Patients with ruptured intracranial aneurysms classified as Hunt and Hess grade 5 (deep coma)

6. Patients with hypersensitivity reactions to the materials used in the coils, such as platinum, tungsten, nickel, or stainless steel

7. Patients with serious adverse reactions to contrast agents

8. Patients who are unable to complete planned follow-up observations due to expected short-term survival or comorbidities

9. Female patients who are pregnant (positive pregnancy test) or planning pregnancy within 12 months after coil placement, or breastfeeding

10. Patients with significant renal dysfunction or uncorrected coagulation disorders

Related Conditions & MeSH terms

• Aneurysm
• Intracranial Aneurysm

Locations

Country	Name	City	State
Korea, Republic of	Severance Hospital	Seoul

Sponsors (1)

Lead Sponsor	Collaborator
Yonsei University

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Anerysm Occlusion Grade : Procedure day Occlusion Grade		Procedure day
Primary	Anerysm Occlusion Grade : 6 month Occlusion Grade		6 months(±30 days) from procedure date
Primary	Anerysm Occlusion Grade : 12 month Occulsion Grade		12 months(±30 days) from procedure date
Primary	Aneurysm Packing Density : Packing Density		Procedure day
Secondary	Neurological complications	Neurological complications related to the use of the device during the procedure	Procedure, 1 month from procedure date
Secondary	Non-neurological complications	Non-neurological complications related to the use of the device during the procedure	Procedure, 1 month from procedure date
Secondary	Device-related events	Device-related events during the procedure (malfunction, stretching, early detachment, etc.)	procedure date
Secondary	Clinical outcomes	Clinical outcomes observed during the follow-up perio	Procedure, 1 month, 6 months, 12 months from procedure date
Secondary	Incidence of recurrence and retreatment	Incidence of recurrence and retreatment during the follow-up period	Procedure, 6 months, 12 months from procedure date