Viewing Study NCT06468150



Ignite Creation Date: 2024-07-17 @ 12:03 PM
Last Modification Date: 2024-10-26 @ 3:32 PM
Study NCT ID: NCT06468150
Status: COMPLETED
Last Update Posted: 2024-06-21
First Post: 2024-06-12

Brief Title: Mechanical Thrombectomy and Catheter Directed Thrombolysis Utilization in Patients With Deep Vein Thrombosis
Sponsor: Pirogov Russian National Research Medical University
Organization: Pirogov Russian National Research Medical University

Study Overview

Official Title: Mechanical Thrombectomy and Catheter Directed Thrombolysis Utilization in Patients With Deep Vein Thrombosis
Status: COMPLETED
Status Verified Date: 2024-06
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 goal of this observational study is to assess the utilization of mechanical thrombectomy and catheter-directed thrombolysis in patients with deep vein thrombosis in tertiary care The main questions it aims to answer are

1 How many patients with deep vein thrombosis are potentially eligible for mechanical thrombectomy and catheter-directed thrombolysis in a tertiary hospital
2 What is the actual number of patients undergoing endovascular interventions for deep vein thrombosis

Participants received endovascular treatment according to the clinical protocol of the treatment
Detailed Description: Tertiary hospital database was analyzed All the records of patients referred for deep vein thrombosis were extracted The collected data included general patient information medical history results of physical examination duplex ultrasound laboratory analysis etc Indications and contraindications for mechanical thrombectomy and catheter-directed thrombolysis were assessed considering possible benefits and risks Patients who could be eligible for this technique were identified

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?: None
Is an FDA AA801 Violation?: None