ClinConnect ClinConnect Logo
Search / Trial NCT06486181

Second Line Endovascular Treatment in Acute DVT

Launched by RUSH UNIVERSITY MEDICAL CENTER · Jun 26, 2024

Trial Information

Current as of July 26, 2025

Not yet recruiting

Keywords

ClinConnect Summary

This clinical trial, titled "Second Line Endovascular Treatment in Acute DVT," is investigating new treatment options for patients with deep vein thrombosis (DVT) who have not improved after a week of standard blood-thinning medications. The study aims to determine whether additional procedures, specifically catheter-directed thrombolysis (a method to break up blood clots using medication) and mechanical thrombectomy (a procedure to remove clots), can be safe and effective for these patients. Participants will be closely monitored with follow-up tests to see how well these treatments work compared to those who only receive the usual care.

To be eligible for the trial, participants must be at least 18 years old, have a recent diagnosis of a specific type of DVT in the leg, and be suitable for blood-thinning treatment. However, patients under 18, those over 75, or anyone with certain medical conditions or risks may not qualify. If you join the study, you will be randomly assigned to either receive the additional treatments or continue with standard care. This research is important because it could lead to better options for patients who need more help with their DVT treatment. The trial is not yet open for enrollment, so keep an eye out for updates if you or a loved one may be interested.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Patients over 18 years of age
  • Patients who have diagnosis of acute femoropopliteal acute deep venous thrombus
  • Patients eligible for anticoagulation treatment
  • Exclusion Criteria:
  • Patients under 18 years of age
  • Patients over 75 years of age
  • Symptoms starting date of more than 14 days
  • Patients who have contraindication for anticoagulation treatment
  • * Patients who have high bleeding risk (more than 2 of the following risk factors):
  • Age \>65 years
  • Previous bleeding
  • Cancer
  • Metastatic cancer
  • Renal failure
  • Liver failure
  • Thrombocytopenia
  • Previous stroke
  • Diabetes
  • Anemia
  • Antiplatelet therapy
  • Poor anticoagulant control
  • Comorbidity and reduced functional capacity
  • Recent surgery in 30 days
  • Frequent falls
  • Hemodynamically unstable patients
  • Patients having severe swelling and pain, cyanosis, and absent pulses consistent with compartment syndrome.

About Rush University Medical Center

Rush University Medical Center is a leading academic medical institution located in Chicago, Illinois, dedicated to advancing healthcare through innovative research and clinical trials. As a sponsor of numerous clinical studies, Rush focuses on translating scientific discoveries into effective treatments and improving patient outcomes across a variety of medical disciplines. With a commitment to excellence in patient care, education, and research, Rush leverages its state-of-the-art facilities and a robust network of specialists to conduct comprehensive trials that adhere to the highest ethical and regulatory standards. Through collaboration with a diverse patient population, Rush aims to enhance the understanding of diseases and develop novel therapeutic strategies.

Locations

Chicago, Illinois, United States

Patients applied

0 patients applied

Trial Officials

Bulent Arslan, MD

Principal Investigator

Rush University Medical Center

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported