Ignite Creation Date:
2024-05-06 @ 8:27 PM
Last Modification Date:
2024-10-26 @ 3:28 PM
Study NCT ID:
NCT06387264
Status:
ACTIVE_NOT_RECRUITING
Last Update Posted:
2024-04-29
First Post:
2024-04-16
Brief Title:
Compont - Varicose Veins of the Lower Extremities
Sponsor:
Peking University Peoples Hospital
Organization:
Peking University Peoples Hospital
Study Overview
Official Title:
Efficacy and Safety of Medical Adhesive in the Treatment of Varicose Veins of the Lower Extremities A Prospective Multicenter Randomized Controlled Study
Status:
ACTIVE_NOT_RECRUITING
Status Verified Date:
2024-09
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The purpose of this clinical trial is to evaluate the effectiveness and safety of Medical Adhesive produced by Beijing Compont Medical Devices Co Ltd in the treatment of varicose veins in the lower extremities
The main questions it aims to answer is What medical problems do participants have when using tissue glue Researchers will compare Medical Adhesive to ClosureFast Endovenous Radiofrequency Ablation RFA Catheter produced by Medtronic Inc to see if Medical Adhesive works to treat varicose veins in the lower extremities
Participants will
Treated with closed varicose veins of the lower extremity by Medical Adhesive or ClosureFast
Return to the hospital at 1 12 and 24 weeks postoperatively for Doppler ultrasound and at 4 12 24 weeks postoperatively for venous scoring
The main questions it aims to answer is What medical problems do participants have when using tissue glue Researchers will compare Medical Adhesive to ClosureFast Endovenous Radiofrequency Ablation RFA Catheter produced by Medtronic Inc to see if Medical Adhesive works to treat varicose veins in the lower extremities
Participants will
Treated with closed varicose veins of the lower extremity by Medical Adhesive or ClosureFast
Return to the hospital at 1 12 and 24 weeks postoperatively for Doppler ultrasound and at 4 12 24 weeks postoperatively for venous scoring
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
False
Is an FDA AA801 Violation?:
None