Clinical trials: Peripheral Vein
Deep Vein Thrombosis, Iliac Vein Thrombosis
Anticoagulant Plus Antiplatelet Therapy Following Iliac Vein Stenting
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…
- Conditions
- Deep Vein Thrombosis, Iliac Vein Thrombosis, Iliac Vein Obstruction, Iliac Vein Stenosis
- Trial name
- NCT04694248
- Testing
- Rivaroxaban, Aspirin
- Where
- China
- Volunteers
- 172 people
- Sponsor
- First Affiliated Hospital of Zhejiang University
Healthy
In Vivo Biomechanical Analysis of the Practitioner's Motion During a Peripheral Venous Catheter Insertion
The aim of this study is to analyze the palpation and perforation motion performed by the practitioner during the insertion of a catheter while measuring the loads applied on the skin and the veins.
- Trial name
- ABGPVVP (NCT03790241)
- Testing
- insertion of a catheter
- Where
- France
- Volunteers
- 31 people, healthy volunteers welcome
- Sponsor
- Hospices Civils de Lyon
Venous Thromboembolism
Dalteparin vs Unfractionated Heparin For The Prevention Of Venous Thromboembolism (VTE) In Hospitalized Acutely Ill Medical Patients
The purpose of this study is to compare the efficacy and safety of dalteparin vs unfractionated heparin for the prevention of VTE (Venous Thromboembolism) in hospitalized acutely ill medical patients.
- Trial name
- NCT00445328
- Testing
- Dalteparin (Fragmin), Unfractionated heparin
- Where
- 7 sites in India
- Volunteers
- 84 people
- Sponsor
- Pfizer
Critical Limb Ischemia, Chronic Limb-Threatening Ischemia
PROMISE I Early Feasibility Trial of the LimFlow Stent Graft System
This pilot study will investigate the safety, effectiveness and feasibility of the LimFlow Stent Graft System for creating an AV fistula in the Below The Knee (BTK) vascular system using an endovascular, minimally invasive…
- Trial name
- NCT03124875
- Testing
- LimFlow System
- Where
- 7 sites in United States
- Volunteers
- 32 people
- Sponsor
- LimFlow, Inc.
Catheter-Associated Infections
Effect of Chlorhexidine Solution in Preventing Peripheral Venous Catheter Associated-Infection
This research aims to determine the most effective chlorhexidine concentration to be used in preventing peripheral venous catheter-associated infections.
- Trial name
- NCT05441605
- Testing
- Effects of Chlorhexidine Solutions with Different Concentrations in Preventing Peripheral Venous Catheter-Associated Infections
- Where
- Turkey (Türkiye)
- Volunteers
- 96 people
- Sponsor
- Aydin Adnan Menderes University
Phlebitis
In-line Filtration Reduces Postoperative Phlebitis.
The aim of this study is to demonstrate the efficacy of in-line filtration in reducing the incidence of postoperative phlebitis associated with peripheral short-term vascular access.
- Trial name
- NCT03193827
- Testing
- In-line filtration, Standard treatment
- Volunteers
- 268 people
- Sponsor
- Careggi Hospital
Catheterization, Peripheral
Compact Closed System Versus Mounted Open System (COSMOS)
The purpose of this study is to investigate, in a prospective and randomized fashion, the clinical performance of a closed intravenous system versus an open conventional one, with respect to ease of handling and effectiveness (as…
- Trial name
- COSMOS (NCT00665886)
- Testing
- Open Intravenous System - Vasocan®, Closed Intravenous System - Nexiva®
- Where
- Spain
- Volunteers
- 1,200 people
- Sponsor
- Hospital San Carlos, Madrid
May-Thurner Syndrome
Rivaroxaban for the Prevention of Deep Vein Thrombosis in Patients With Left Iliac Vein Compression - The PLICTS Study
The purpose of this study is to evaluate the efficacy and safety of rivaroxaban for the prevention of deep vein thrombosis in patients with left iliac vein compression treated with stent implantation.
- Trial name
- PLICTS (NCT04067505)
- Testing
- Rivaroxaban, Warfarin, Nadroparin
- Where
- 9 sites in China
- Volunteers
- 224 people
- Sponsor
- Second Affiliated Hospital, Zhejiang University, School of Medicine
Deep Venous Thrombosis
Biomarker Sub Study of the Compression Stockings to Prevent the Post-Thrombotic Syndrome (SOX) Trial
The purpose of this study is to evaluate whether biomarkers of inflammation, genetic thrombophilia and coagulation activation influence Post-Thrombotic Syndrome development in patients with symptomatic proximal deep venous…
- Trial name
- Bio-SOX (NCT01615705)
- Where
- 25 sites in United States, Canada
- Volunteers
- 803 people
- Sponsor
- Sir Mortimer B. Davis - Jewish General Hospital
Shock, Peripheral Venous Catheterization
Pulse Study: Peripheral Use of Low-dose Vasopressors for Safety and Efficacy in the Intensive Care Unit
Using medications to increase blood pressure, called vasopressors, is invaluable in treating patients who have difficulty maintaining stable blood pressure.
- Conditions
- Shock, Peripheral Venous Catheterization, Central Venous Catheterization, Critically Ill Patients Admitted in ICU
- Trial name
- PULSE (NCT06920173)
- Testing
- Experiemental: Peripheral Venous Catheter
- Where
- Canada
- Volunteers
- 50 people
- Sponsor
- Kingston Health Sciences Centre
Vascular Access
Accuvein Versus Standard Care for Intravenous Cannulation Procedure in Children
Peripheral intravenous cannulation is one of the most common procedures performed in children admitted to hospital. It is a painful and anxiety-provoking gesture for children with possible memorization of the pain even more…
- Trial name
- AVEn (NCT03427723)
- Testing
- Accuvein®400, Standard care
- Where
- France
- Volunteers
- 300 people
- Sponsor
- University Hospital, Clermont-Ferrand
Peripheral Arterial Disease, Peripheral Artery Disease
FRAME, External Support for Lower Limb Autologous Grafts
30 patients will be enrolled in a prospective, multi-center, one-arm study, enrolling patients with claudication and chronic limb ischemia scheduled for lower limb venous bypass grafting on clinical grounds with single segment…
- Trial name
- NCT04003480
- Testing
- FRAME
- Where
- 3 sites in United States
- Volunteers
- 30 people
- Sponsor
- Vascular Graft Solutions Ltd.
CRPS Type II
Surgical Treatment Of Complex Regional Pain Syndrome Type II (CRPS II)
The purpose of this study is to investigated and evaluated the effectiveness of a new surgical technique for the treatment of severe chronic pain stages (Complex Regional Pain Syndrome Type II).
- Trial name
- NCT01392599
- Testing
- SUBCUTANEOUS VENOUS SYMPATHECTOMY (RSVS)
- Where
- Austria
- Volunteers
- 20 people
- Sponsor
- Medical University of Vienna
Venepuncture
Evaluation of a Touchless Vein Scanner for Venepuncture and Cannulation in Pediatric Patients
Evaluation of the AccuVein ® AV 300 vein scanner in clinical routine in a pediatric operation room setting for a 4 weeks period.
- Trial name
- VENSCAN (NCT01434537)
- Where
- Germany
- Volunteers
- 238 people
- Sponsor
- Charite University, Berlin, Germany
Peripherial Venous Pressure, Central Venous Pressure
Peripheral Venous Pressure as an Indicator of Central Venous Pressure in Post Operative Surgical Patients: A Randomised Controlled Trial
The study is aimed at comparing peripherial venous pressure as an indicator of central venous pressure in post operative surgical patients.
- Conditions
- Peripherial Venous Pressure, Central Venous Pressure, Fluid/Volume Status Monitoring of Patient
- Trial name
- NCT05476666
- Testing
- Peripherial and central venous access
- Where
- Pakistan
- Volunteers
- 40 people
- Sponsor
- Pakistan Navy Station Shifa Hospital
Malaria, Vivax
A Study to Assess the Effects of Dissolution Profile on the Pharmacokinetics of Single Oral Doses of Tafenoquine Tablets and Tafenoquine Stable Isotope Labelled Solution
This study will investigate the effect of Tafenoquine (TQ) 150 mg tablet ageing (dissolution profiles) on human exposure of TQ comparing the relative bioavailability of TQ from tablets exhibiting different dissolution profiles in…
- Trial name
- NCT02751294
- Testing
- Tafenoquine Control, Tafenoquine dissolution profile X, Tafenoquine SIL
- Where
- United States
- Volunteers
- 14 people, healthy volunteers welcome
- Sponsor
- GlaxoSmithKline
Pediatrics, Immobilization
Immobilization During Peripheral Venous Catheter Placement
Aim: To determine the most effective type of upper limb immobilization in the cannulation of a peripheral venous line in the pediatric emergency department.
- Trial name
- NCT07182994
- Testing
- Elbow joint immobilization, Arm restraint without elbow immobilization
- Where
- Spain
- Volunteers
- 322 people, healthy volunteers welcome
- Sponsor
- Hospital Universitario La Paz
All Patients with Peripheral Venous Catheters
Care Bundle Applıcation in the Prevention of Phlebitis
This study was designed as a non-randomized controlled trial, comprising both experimental and control groups, to evaluate the efficacy of an evidence-based care bundle in preventing the development of peripheral venous…
- Trial name
- Non-randomized (NCT06743399)
- Where
- Turkey (Türkiye)
- Volunteers
- 116 people
- Sponsor
- Karamanoğlu Mehmetbey University
Peripheral Venous Outflow Obstruction
Sinai Vein Stent Registry
The Sinai Vein Stent Registry aims to establish and maintain a registry of patients who have undergone a vein stent placement procedure at The Mount Sinai Medical Center.
- Trial name
- NCT02600936
- Testing
- vein stent placement
- Where
- United States
- Volunteers
- 1,000 people
- Sponsor
- Windsor Ting
Peripheral Artery Occlusive Disease, Peripheral Artery Restenosis
Drug-eluting Balloon vs. Conventional Balloon in the Treatment of (re)Stenosis - a Randomized Prospective Study
The purpose of this study is to determine whether the use of drug-eluting balloons is effective in the treatment of (re)stenosis in bypass vein grafts.
- Conditions
- Peripheral Artery Occlusive Disease, Peripheral Artery Restenosis, Peripheral Artery Stenosis
- Trial name
- DRECOREST1 (NCT03023098)
- Testing
- Conventional PTA, Drug-eluting balloon
- Where
- Finland
- Volunteers
- 57 people
- Sponsor
- Helsinki University Central Hospital