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Vascular Access Complication clinical trials

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NCT ID: NCT04409418 Completed - Clinical trials for Vascular Access Complication

Blood Sampling Functionality of Extended Dwell Catheters

Start date: June 23, 2021
Phase: N/A
Study type: Interventional

The purpose of this study is to compare upper arm versus forearm Extended Dwell Catheter (EDC) placement for blood sampling functionality. EDC is an alternative to peripheral Intravenous (IVs) especially during prolonged hospital stays. EDCs are generally placed using ultrasound for guidance and are commonly placed in any of 3 veins in the arm. They can be inserted above or below the antecubital fossa (the bend of the elbow). These catheters can be left for up to 30 days and don't fail as quickly when compared to peripheral IVs.

NCT ID: NCT03986151 Completed - Clinical trials for Coronary Artery Disease

Anatomical sNuffbox for Coronary anGiography and IntervEntions

ANGIE
Start date: June 11, 2019
Phase: N/A
Study type: Interventional

This randomized, single-center, prospective study seeks to compare the conventional radial approach with the recently described distal radial approach (anatomical snuffbox) concerning the patency of the radial artery in patients subjected to coronary angiography or percutaneous coronary intervention.

NCT ID: NCT03969225 Completed - Clinical trials for Vascular Access Complication

Vascular Access Outcome Measure for Function: a vaLidation Study In haemoDialysis

VALID
Start date: December 6, 2019
Phase:
Study type: Observational

A functioning vascular access provides a lifeline for patients requiring haemodialysis but vascular access dysfunction remains one of the leading causes of excessive morbidity, mortality and healthcare costs in this group. Despite increasing numbers of vascular access trials, successful interventions to improve vascular access function have been sparse and compromised by highly variable, often selectively reported outcome measures of limited relevance to patients and health professionals. Through engagement of all relevant stakeholders including patients and caregivers, vascular access function, defined by the need for interventions to enable and maintain the use of a vascular access for haemodialysis, has been identified as one of the most critically important outcome measures for trials in haemodialysis. This prospective, multi-centre, multinational validation study aims to assess the accuracy and feasibility of measuring vascular access function part of routine clinical practice and across different clinical settings to ensure successful global implementation of this core outcome measure in future trials in haemodialysis.

NCT ID: NCT03656978 Completed - Clinical trials for Perioperative/Postoperative Complications

Ultrasound-Guided Vascular Puncture and Catheterization

UGVPC
Start date: June 1, 2017
Phase: N/A
Study type: Interventional

To assess and improve the safety and success rate of vascular puncture and catheterization using ultrasound-guided methods.

NCT ID: NCT03393052 Completed - Clinical trials for Coronary Artery Disease

Left Radial comparEd to Femoral Approach for CORonary Angiography in Patients With Previous CABG StuDy

L-RECORD
Start date: January 20, 2017
Phase: N/A
Study type: Interventional

This randomized, multicenter, prospective study seeks to compare left radial and femoral access during cardiac catheterization of patients with prior history of CABG surgery, with the primary objective of demonstrating that the two access techniques do not differ in the net procedure time (non-inferiority study) expanding the documented benefits of radial access to this group of patients.

NCT ID: NCT03326739 Completed - Clinical trials for Vascular Access Complication

Ultrasound Guided Versus Landmark Guided Arterial Line Placement by Emergency Medicine Interns

Start date: January 1, 2017
Phase: N/A
Study type: Interventional

Critically ill patients in the emergency department commonly require arterial line placement for continuous direct blood pressure monitoring, frequent arterial blood gas sampling, and frequent blood sampling. Trans-radial catheterization has been shown to reduce access site complications and increase patient comfort compared to trans-femoral access. Radial artery access on the first attempt is optimal; attempts at reentry delay care and increase the risk of vascular spasm, hematoma, infection, neurovascular injury, and pain. The traditional pulse palpation method of radial artery cannulation can be challenging, especially in patients with weak pulses (i.e. morbidly obese or hypotensive individuals). A review of literature suggests that ultrasound guided trans-radial catheterization compared to standard pulse palpation reduces access time and increases rate of first-entry success when performed by physicians trained in ultrasound. Thus, complications ascribed to reentry are prevented and timely care is provided. To the investigator's knowledge, only one other prospective study has been conducted to assess the utility of ultrasound guided radial artery cannulation in the emergency department. Due to the paucity of literature to support the use of ultrasound guided trans-radial catheterization in critically ill patients, the study will aim to provide further data on the topic. Both techniques are considered standard of care.

NCT ID: NCT03036241 Completed - Clinical trials for Vascular Access Complication

Drug-eluting Balloon vs. Conventional Balloon in the Treatment of (re)Stenosis (Dialysis Fistulae)

DRECOREST2
Start date: January 23, 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether the use of drug-eluting balloons is effective in the treatment of (re)stenosis in dialysis fistulae.

NCT ID: NCT02558153 Completed - Clinical trials for Vascular Access Complication

RCT of Paclitaxel DEB Compared to Standard PTA in Dialysis Fistula

APERTO
Start date: June 2015
Phase: N/A
Study type: Interventional

A multicenter randomized clinical trial of paclitaxel drug-eluting balloon (DEB) versus standard percutaneous transluminal angioplasty (PTA) to reduce restenosis in 150 patients with haemodialysis access stenoses.

NCT ID: NCT02513303 Completed - Clinical trials for End Stage Renal Disease

Trial to Evaluate the Sirolimus-Eluting Collagen Implant on AV Fistula Outcomes

ACCESS
Start date: November 2015
Phase: Phase 3
Study type: Interventional

The objective of this study is to evaluate efficacy and safety outcomes following use of the Sirolimus-eluting Collagen Implant (SeCI) in subjects undergoing surgical creation of an AV fistula for vascular access (index procedure).

NCT ID: NCT02405728 Completed - Clinical trials for Vascular Access Complication

Vascular Access in Hematological Patients - PICC Versus CVC

Start date: February 2015
Phase: N/A
Study type: Interventional

The use of peripherally inserted central catheters (PICCs) represents a major advance for hematological patients, enabling the effective delivery of chemotherapy and/or blood products particularly for prolonged infusions or in situation of difficult venous access. In modern medical practice their use has increased rapidly for several reasons, including ease of insertion, many uses (e.g., drug administration and venous access), perceived safety, and cost-effectiveness compared with centrally inserted central catheters (CICCs).