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Central Venous Catheterization clinical trials

View clinical trials related to Central Venous Catheterization.

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NCT ID: NCT03442790 Not yet recruiting - Clinical trials for Central Venous Catheterization

Agitated Saline Versus CXR Confirmation of Central Venous Lines

Start date: May 1, 2018
Phase: N/A
Study type: Interventional

Central venous lines insertion are common procedures these days. CVL placed under USG guidance have high success rates and low complications even in developing country settings. However, the investigators still have to rely on chest x-ray (CXR) to confirm the correct placement of central venous lines as a gold standard method. This might be time consuming and may cause delay in initiation of treatment. In some cases, as in operating room, the treatment is started even before confirmation by CXR. Ultrasound has ability to localize the tip of the catheter at the superior venacava- right atrium junction using agitated saline and the appearance of contrast within 2 seconds in right atrium. However, this technique is rarely used. The investigators, therefore, designed the trial to study whether confirmation of tip of CVL by ultrasound is non-inferior to the CXR confirmation.

NCT ID: NCT03395691 Completed - Clinical trials for Central Venous Catheterization

Comparison of the Proximal Approach and Distal Approach of Axillary Vein Catheterization Under Ultrasound Guidance

Start date: February 11, 2018
Phase: N/A
Study type: Interventional

Ultrasound-guided axillary vein catheterization can be performed via the proximal or distal approach of the axillary vein. The aim of our study is to compare the first puncture success rate and safety between the two approaches of ultrasound-guided axillary vein catheterization in cardiac surgical patients with risk of bleeding.

NCT ID: NCT03348826 Withdrawn - Cancer Clinical Trials

Study of Sodium Bicarbonate in Restoring Blocked Catheters

Start date: June 1, 2020
Phase: Phase 2
Study type: Interventional

This is a study looking at the use of sodium bicarbonate to restore the flow of blocked central line devices in patients with blood cancers. Central line devices uses thin tubes that are placed into a vein in the body to give medicines, fluids, nutrients, blood products, etc. Sometimes, the lines become blocked. The standard procedure to get the line working again is to use alteplase, a protein that dissolves blood clots. While blood clotting is one cause of a blocked line, other reasons included the formation of calcium deposits. Sodium bicarbonate is routinely used in the treatment of patients receiving chemotherapy. Sodium bicarbonate is a liquid drug which is capable of dissolving protein and calcium deposits. This study will compare whether sodium bicarbonate works just as well as alteplase to recover the function of a blocked line.

NCT ID: NCT02939690 Completed - Clinical trials for Central Venous Catheterization

Umbilical Venous Catheter Insertion Depth in Neonates

Start date: October 2016
Phase: N/A
Study type: Interventional

In this randomized clinical study, neonates who require umbilical venous catheter (UVC) insertion as part of their routine care at anytime during their NICU admission will be randomized to one of the 2 formulas for estimation of the pre-insertion UVC depth (umbilicus to the nipple in cm minus 1 (UN - 1) or birth weight based formula ([(3× birth weight (Kg) + 9)/2+1)]. UVC will be inserted under sterile condition as per unit protocol. To verify the UVC tip position, a thoracoabdominal radiograph will be taken. In addition, the investigators will do a ultrasound of the heart to assess the exact location of the catheter tips as soon as possible but within 6 hours of insertion.

NCT ID: NCT02741453 Completed - Critical Care Clinical Trials

Bilateral Internal Jugular Veins Ultrasound Scanning Prior to CVC Placement

BIUS
Start date: September 1, 2016
Phase: N/A
Study type: Interventional

Central venous catheter placement is a common procedure in the intensive care unit and is a required skill for all residents working in the critical care setting. Central venous catheters (CVC) are placed for a variety of reasons including administration of caustic medications, administration of fluids or blood products for rapid resuscitation, access for hemodynamic monitoring or transvenous pacing, temporary vascular access for dialysis, or inability to obtain peripheral IV access. CVC's are routinely placed in the internal jugular vein in the Vanderbilt medical ICU and ultrasound guidance is used. Placement of the CVC on the right IJ instead of the left IJ is commonly preferred due to the more direct path to the superior vena cava. However, placement in the left IJ may be necessary for a variety of reasons. The investigators intend to compare the standard practice of residents and nurse practitioners placing IJ CVCs in the medical ICU against mandatory screening of the right and left IJ prior to selection of the CVC placement site. The investigators will accomplish this by assessing the relative first pass stick and overall success rates, the rate of aborted procedures, and the rate of complications between standard practice and mandatory screening of bilateral internal jugular veins prior to CVC site selection.

NCT ID: NCT02661607 Completed - Critical Care Clinical Trials

Point of Care Echocardiography Versus Chest Radiography for the Assessment of Central Venous Catheter Placement

Start date: October 2014
Phase: N/A
Study type: Interventional

A prospective study to compare the use of point of care echocardiography versus routine chest radiography for the assessment of central venous catheter placement.

NCT ID: NCT02264964 Not yet recruiting - Venous Thrombosis Clinical Trials

Duration and Adverse Events of Non-cuffed Catheter in Patients With Hemodialysis

DACAPO
Start date: January 2015
Phase: N/A
Study type: Interventional

The duration and adverse events of non-cuffed catheter in patients with hemodialysis will be investigated by multicenter prospective cohort. Totally, 1,400 patients with chronic renal failure requiring hemodialysis will be enrolled. 900 patients will be given right internal jugular catheterization, and the other 500 patients unsuitable for right internal jugular catheterization will receive femoral catheterizations. Every patient will be followed-up for six months. During following-up period, the duration time and adverse events of non-cuffed catheter will be recorded in details, including inadequate hemodialysis blood flow, venous stenosis, venous thrombosis, infection, catheter thrombosis and so on. The central vein will be evaluated by CT Angiography to identify its stenosis at last visit after 6 months. This multicentre trial will provide evidence to develop guideline for duration time of using non-cuffed catheter.

NCT ID: NCT01543360 Completed - Clinical trials for Central Venous Catheterization

Comparison of Axillary Versus Subclavian Vein Strategies for Central Venous Catheterization Under Continuous Ultrasound Guidance

Start date: June 2012
Phase: N/A
Study type: Interventional

The main objective of this study is to compare the rate of successful establishment of a central venous catheter in the first two attempts of ultrasound-guided puncture between two techniques: (1) a subclavian technique versus (2) an axillary technique.

NCT ID: NCT01003366 Completed - Clinical trials for Central Venous Catheterization

Effect of the Bevel Direction of Puncture Needle on Success Rate and Complications During Central Venous Catheterization

Start date: March 2009
Phase: N/A
Study type: Interventional

To test the hypothesis that approaching the internal jugular vein with the needle bevel down would produce less injury to the vessel wall compared to the bevel up approach during central venous catheterization.