Anticoagulant Plus Antiplatelet Therapy Following Iliac Vein Stenting

NCT04694248 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 172

Last updated 2025-09-25

No results posted yet for this study

Summary

To evaluate the efficacy and safety of combination of anticoagulant and antiplatelet therapy on the patency of iliac vein at 12-month post stenting in patients with acute proximal DVT and ipsilateral iliac vein stenosis who received percutaneous mechanic thrombectomy and iliac vein stenting.

Conditions

  • Deep Vein Thrombosis
  • Iliac Vein Thrombosis
  • Iliac Vein Obstruction
  • Iliac Vein Stenosis
  • Iliac Vein Compression Syndrome

Interventions

DRUG

Rivaroxaban

For anticoagulant, it is rivaroxaban 20mg once a day for 6 months.

DRUG

Aspirin

For antiplatelet therapy, it is aspirin 100mg once a day indefinitely.

Sponsors & Collaborators

  • Zhejiang University

    collaborator OTHER
  • Ningbo No.2 Hospital

    collaborator OTHER
  • Taizhou Hospital of Zhejiang Province affiliated to Wenzhou Medical University

    collaborator OTHER
  • The Central Hospital of Lishui City

    collaborator OTHER
  • Taizhou Enze Medical Center Group

    collaborator OTHER
  • Taizhou First People's Hospital

    collaborator OTHER
  • Boston Scientific Corporation

    collaborator INDUSTRY
  • First Affiliated Hospital of Zhejiang University

    lead OTHER

Principal Investigators

  • Hongkun Zhang, M.D. · First Affiliated Hospital of Zhejiang University

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-11-03
Primary Completion
2026-12-31
Completion
2027-06-30

Countries

  • China

Study Locations

More Related Trials

Entities

Drugs

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04694248 on ClinicalTrials.gov