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NCT ID: NCT05909605 Completed - Medical Device Clinical Trials

Clinical Feasibility of a Conformal Ultrasound Blood Pressure Sensor

Start date: October 20, 2020
Phase:
Study type: Observational

Blood pressure (BP) monitoring is essential for managing cardiovascular diseases. Arterial line (A-line), the clinical gold standard for BP monitoring, is too invasive for routine measurements. The sphygmomanometer, on the other hand, is non-invasive but captures only discrete values. The recently introduced conformal ultrasound sensor offers non-invasive and continuous monitoring of BP, which can potentially improve the quality of patient care, but its accuracy has yet to be thoroughly validated. Here the investigators are working to validate the accuracy of a redesigned ultrasound sensor with enhanced reliability in BP measurements at-home and in clinics even under different interventions.

NCT ID: NCT05329246 Completed - Clinical trials for Cardiovascular Diseases

Validation of PMcardio AI-assisted Clinical Assistant in Primary Care

PMCARDIO-PT1
Start date: November 22, 2021
Phase: N/A
Study type: Interventional

This study aimed to analyze and investigate whether the use of the PMcardio clinical assistant leads to a more efficient patient management in primary care and more accessible specialised care compared to usual standards of care and to assess the reliability and safety of the PMcardio smartphone application in the primary care use environment. Additionally, to evaluate time savings and cost saving implications of increased availability of specialised care at the primary care level.

NCT ID: NCT04012437 Completed - Clinical trials for Premature Ejaculation

Efficacy of App and Electronic Device in the Treatment of Premature Ejaculation

Start date: July 1, 2019
Phase: N/A
Study type: Interventional

Randomized control trial to determine if we can produce increases in the IELT using a new masturbator electronic in subjects with premature ejaculation in combination with a exercise app, producing improvements in the quality and satisfaction of the sexuality of the patient.

NCT ID: NCT04006899 Completed - Medical Device Clinical Trials

Development of a Segmental Bioelectrical Impedance Spectroscopy Device for Body Composition Measurement

Start date: June 20, 2018
Phase:
Study type: Observational

A device for measuring body composition with a small electric current, at 200 μA, (bioelectrical impedance analysis, or BIA) was designed. The goal of this study is to validate the device against several existing devices using the same method of measuring body composition with a small electric current.

NCT ID: NCT03781232 Completed - Diabete Mellitus Clinical Trials

Non-invasive Glucose Measurement With Raman Technology in Patients With Type 1 and Type 2 Diabetes

Start date: November 22, 2018
Phase: N/A
Study type: Interventional

The study was established to collect data and reference measurements in order to establish calibration models for the Prototype 0.3

NCT ID: NCT03443349 Completed - Medical Device Clinical Trials

"Vibwife One" a New Medical Device to Support Delivering Women in Their Mobilization

Start date: January 23, 2018
Phase: N/A
Study type: Interventional

"Vibwife One" was developed to support the mobilization of the delivering women during the labor process. It consists of a mattress that fits on existing delivery beds. Different movements, adjustable in pace and intensity can be chosen to mobilize women in labor. Although existing evidence is rare, some literature and historical reports have shown a positive impact of active mobilization during labor. At time of rising epidural anesthesia rate, "Vibwife One" could be an interesting way to active mobilize those women to support the physiological birth process. So far, the device has not yet been applied in delivering women. The investigators carry out a first safety study to assess the safety, to evaluate the comfort and the practicability for delivering women and medical staff of this new medical device.

NCT ID: NCT00708058 Completed - Clinical trials for Congestive Heart Failure

Use of Defibrillator Information in the Emergency Department

Start date: August 2007
Phase: N/A
Study type: Observational

This is a study to determine the feasibility of obtaining information stored in existing Medtronic internal defibrillators in patients who present to the Emergency Department(ED) for any reason. In addition, the study will determine if this information is useful to the ED physician in managing the patient's care, specifically as it relates to heart failure.

NCT ID: NCT00486681 Completed - Diabetes Mellitus Clinical Trials

Clinical Assessment of an in-Patient Glucose Monitoring System (Accu-Chek Inform Cobas IT 1000)

COBAS
Start date: January 2007
Phase: N/A
Study type: Observational

The principal objective of this single-center 2-period study is to evaluate the glycemic control of in-patients in 3 hospital departments (Diabetology, Cardiology and Pulmonary Care) as the rate of capillary blood glucose measurements within a pre-define target range, and to compare results during the period I (warning of the Accu-Check Inform glucose meter on glucose levels not activated) and period II (warning activated).