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Bradycardia clinical trials

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NCT ID: NCT03132688 Completed - Clinical trials for Anesthesia; Functional

A Study on Safety and Efficacy of Propofol in Small Children Under 2 Years of Age

Start date: April 20, 2017
Phase: N/A
Study type: Observational

This retrospective study the safety and efficacy of intravenous propofol used in children under 2 years of age during general anesthesia for surgery.

NCT ID: NCT03065309 Completed - Hypotension Clinical Trials

Determination of Remifentanil's ED50 for Rapid Sequence Intubation Avoiding Bradycardia and Hypotension in Adults

Start date: February 25, 2017
Phase: Phase 3
Study type: Interventional

This study will find the median effective dose of remifentanil for rapid sequence intubation which avoids bradycardia and hypotension

NCT ID: NCT03053609 Completed - Clinical trials for Gastroesophageal Reflux Disease

Gastroesophageal Reflux and Cardiorespiratory Problems

CR-GER
Start date: January 2006
Phase: N/A
Study type: Observational

Cardiorespiratory and gastroesophageal reflux events often coexist in infants in Neonatal Intensive Care Unit (NICU) thus leading to drugs over-prescription and delayed discharge. Through cardiorespiratory and pH-impedance monitoring this study aims to evaluate the temporal association between gastroesophageal reflux (GER) and cardiorespiratory (CR) events in a large number of infants with gastroesophageal reflux disease (GERD) and CR symptoms and, whether this association is significant, to clarify the impact of GER on CR events.

NCT ID: NCT03012568 Completed - Bradycardia Clinical Trials

Clinical Study to Confirm MRI Safety and Effectiveness Using St. Jude Medical (SJM) Cardiac Rhythm Management Systems

ASSUREMRI
Start date: November 10, 2016
Phase:
Study type: Observational

This is a clinical investigational plan (CIP) for the "Clinical Study to Confirm MRI Safety and Effectiveness Using SJM Cardiac Rhythm Management Systems (ASSURE MRI)". This study intends to enroll patients who meet standard bradycardia or tachycardia indications and have already been implanted with one of the SJM device/lead combinations listed in this protocol. The objective of this study is to confirm the safety and effectiveness of each of the four SJM device/lead combinations in an MRI environment. This clinical investigation is sponsored by St. Jude Medical.

NCT ID: NCT02930980 Completed - Bradyarrhythmia Clinical Trials

Micra Accelerometer Sensor Study 2

MASS2
Start date: October 14, 2016
Phase: N/A
Study type: Interventional

The purpose of the MASS2 is to characterize accelerometer signals of Micra implantable device during different postures and activities and to understand the source of the sensed motion, in order to test feasibility for future enhancements in device functionalities.

NCT ID: NCT02863666 Completed - Bradycardia Clinical Trials

Verification of Prediction Algorithm

VPAC
Start date: August 11, 2016
Phase:
Study type: Observational

Prospective observational clinical study to verify an algorithm used to predict cardiopulmonary events in patients presenting to the emergency department.

NCT ID: NCT02858583 Completed - Bradycardia Clinical Trials

SI + CC Versus 3:1 C:V Ratio During Neonatal CPR

SURV1VE
Start date: October 19, 2017
Phase: N/A
Study type: Interventional

Research question In newborn infants requiring CPR, does CC superimposed by sustained inflation compared to 3:1 compression to ventilation ratio improves return of spontaneous circulation? Overall objective: CC superimposed by sustained inflation will improve short- and long-term outcomes in preterm (>28 weeks or older) and term newborns. Hypothesis to be tested Primary hypothesis: By using CC superimposed by sustained inflation (CC+SI) during CPR the time needed to achieve return of spontaneous circulation (ROSC) compared to the current 3:1 compression to ventilation (C:V) will be reduced in asphyxiated newborns.

NCT ID: NCT02764970 Completed - Bradycardia Clinical Trials

Heart Rate Reducing Therapy in Cardiac CT Using Ivabradine and Bisoprolol

Start date: February 2015
Phase:
Study type: Observational

Out-patients scheduled for coronary computer tomographic angiography (CCTA) were screened regarding their baseline heart rate. If heart rate was > 75, patients were pretreated with 10mg bisoprolol (group 1) or 10mg bisoprolol plus 7.5mg ivabradine (group 2) to reduce heart rate one our before CCTA was performed. Heart rate, additional use of i.v. bradycardic agents, motion artefacts, radiation dose and drug tolerance was monitored.

NCT ID: NCT02758210 Completed - Clinical trials for Bradycardia, Atrial Tachyarrhythmia

Evaluating the Electro Magnetic Interference of Using Tablet and Smart Phone on Leadless Pacemaker (MICRA)

MICRA
Start date: April 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the effects that electromagnetic field exposure from using a tablet and smart phone have on a leadless pacemaker (MICRA device).

NCT ID: NCT02676011 Completed - Bradycardia Clinical Trials

Brad Arrhythmia Induced by Repeated Succinylcholine During Gynecological Laparoscopic Surgery

Start date: February 2016
Phase: Phase 2
Study type: Interventional

Cardiac arrhythmias are a well-recognized complication of anesthesia for laparoscopy. The aim of this study was to evaluate the efficacy of atropine sulfate for prevention of brad arrhythmia induced by repeated succinylcholine during gynecological laparoscopic surgery.