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NCT ID: NCT03967587 Terminated - Oxygen Saturation Clinical Trials

Evaluation of Intravascular Monitoring of Partial PRessure of Oxygen for Neonatal intensiVE Care Patients

IMPROVE
Start date: November 19, 2020
Phase: N/A
Study type: Interventional

The study is a non-blinded trial with one single intervention in sick newborn infants. The Neosense umbilical catheter will be used instead of the routinely used umbilical catheter on infants where the treating physician has ordered use of an umbilical catheter. The catheter will be connected to the Neosense monitor/measuring unit. Blood samples for blood gas analysis are collected from the patients according to the clinical routine (every 4th to 6th hour). Oxygen tension data from the Neosense measuring system, from the time points when a blood gas sample was collected, will be recorded. This data will be compared to the oxygen tension value from the blood gas sample collected at the same time point. The blood gas samples will be analysed according to clinical and laboratory routine. The infants will remain in the study as long as the Neosense measuring system is used.

NCT ID: NCT03642756 Not yet recruiting - Catheters Clinical Trials

Effects of Different Intra-arterial Catheter Size on Frequency of Optimal Dynamic Response in Radial Arterial Waveform

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

The aim of this study is to compare the effects of different intra-arterial catheter size on the frequency of optimal dynamic response in radial arterial waveform.

NCT ID: NCT03106389 Recruiting - Misoprostol Clinical Trials

Misoprostol With And Without Transcervical Balloon Catheter In Second Trimester Termination Of Pregnancy

Start date: March 1, 2017
Phase: Phase 4
Study type: Interventional

This randomized controlled study will be performed to compare the benefits and risks associated with the administration of misoprostol with or without the use of a transcervical balloon catheter to terminate pregnancy in the second trimester (defined as gestational age between 14 and 28 weeks of gestation).

NCT ID: NCT02769442 Completed - Clinical trials for Catheterization, Peripheral

Prospective, Randomized Controlled Comparison of TERUMO SurFlash Plus Versus BD Insyte Autoguard in an Urban ED

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

A randomized prospective comparison of two FDA approved intravenous catheters in the emergency department setting. The Terumo SurFlash Plus offers novel technologies that promise to increase intravenous access success rates and decrease blood contamination of the insertion site. This study would analyze these properties in our busy, urban emergency department setting where time and safety of intravenous access are most critical.