Peripheral Arterial Disease
Conditions
Keywords
Peripheral Arterial Disease
Brief summary
The purpose of this study is to evaluate the safety and efficacy of interlocking detachable coils system in the treatment of Chinese patients with embolization of peripheral arterial in comparison with Interlock Fibered IDC Occlusion System
Detailed description
This is a prospective, multicenter, open-label, non-inferiority, randomized controlled clinical trial. The plan is to recruit patients with peripheral arterial disease requiring embolization and then perform peripheral arterial embolization based on randomization using devices in the experimental group or control group. This trail will be conducted in a number of experimental institutions in China, and a total of 116 subjects are planned to be enrolled. All subjects were treated with the interlocking detachable coils system and were evaluated during surgery and before discharge from the treatment of experimental or control devices, followed up at 1 month, 3 months, and 6 months after surgery.
Interventions
DEVICEInterlocking detachable coils system
Mainly used to block or slow blood flow in the peripheral vascular system during embolization procedures.
DEVICEInterlock Fibered IDC Occlusion System
Mainly used to block or slow blood flow in the peripheral vascular system during embolization procedures.
Sponsors
Shanghai Shenqi Medical Technology Co., Ltd
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No
Inclusion criteria
1. Age 18-80 years; 2. Subject diagnosed with peripheral arterial embolization by preoperative imaging (CTA); 3. The target vessel can be embolized in one operation; 4. The visual diameter of the target blood vessel is 5mm-30mm; 5. Subjects or their legal representatives can understand the purpose of the trial, voluntarily participate and sign the written informed consent, and can be followed up.
Exclusion criteria
1. Definite allergy, resistance or contraindication to antiplatelet agents, anticoagulants, contrast agents and/or anesthetics; 2. Definite allergy to platinum, tungsten and/or any substance in the test coil; 3. Subjects are not suitable for anesthesia or endovascular surgery, such as those with severe respiratory, heart, lung, liver, kidney disease or coagulation disorders (such as hemophilia); 4. The target vessel has undergone previous surgery and/or major cardiovascular surgery within 3 months; 5. The target aneurysm is dissecting aneurysm, infected aneurysm, ruptured aneurysm, and aneurysm caused by connective tissue disease; 6. Women who are pregnant or breastfeeding; 7. Subjects who are participating in clinical trials of other drugs or devices that have not reached the end point of the trial; 8. The researcher believes that it is not suitable to participate in the trial.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| target vessel occlusion rate | 6 months | no blood flow through the occluded segment of the target vessel |
Countries
China
Outcome results
None listed