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Clinical Trials/NCT05521100
NCT05521100
Not yet recruiting
Not Applicable

Comparison of Safety and Efficacy Between the Application of Vascular Closure Device and Conventional Figure-of-eight Suture in Transvenous Cardiac Interventional Surgery

Shanghai 10th People's Hospital1 site in 1 country160 target enrollmentSeptember 30, 2022
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ConditionsVascular Access Complications

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Vascular Access Complications
Sponsor
Shanghai 10th People's Hospital
Enrollment
160
Locations
1
Primary Endpoint
Vascular bleeding event rate
Status
Not yet recruiting
Last Updated
3 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSitesSimilar Trials

Overview

Brief Summary

Comparison of safety and efficacy between the application of vascular closure device and conventional figure-of-eight suture in transvenous cardiac interventional surgery

Detailed Description

Comparison of safety and efficacy between the application of vascular closure device and conventional figure-of-eight suture in transvenous cardiac interventional surgery.From the operation success rate, postoperative bleeding, immobilization time, the rate of revisiting the doctor due to wound problems within 1 month, etc.

Registry
clinicaltrials.gov
Start Date
September 30, 2022
End Date
December 1, 2023
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Shanghai 10th People's Hospital
Responsible Party
Principal Investigator
Principal Investigator

Ya-Wei Xu

Director of Cardiology

Shanghai 10th People's Hospital

Eligibility Criteria

Inclusion Criteria

  • •Patients receiving lower extremity venous intervention with a diameter of 12F or more

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Vascular bleeding event rate

Time Frame: 1month

Proportion of bleeding after two methods of vascular suturing

Secondary Outcomes

  • bed braking time(1 day)

Study Sites (1)

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