Clinical trials: Device
Glaucoma
Automatic Evaluation of the Anterior Chamber Angle Width by a New Non-contact Optical Device
The aim of the study is to evaluate an objective, non-invasive optical device able to quantify, without eye contact, the width of the irido-corneal angle and to better identify cases of narrow angle or angle closure that may be…
- Trial name
- NCT06278597
- Testing
- NACA Estimator
- Where
- Italy
- Volunteers
- 64 people, healthy volunteers welcome
- Sponsor
- Fondazione G.B. Bietti, IRCCS
Sleep Disorder
Accuracy Evaluation of EarlySense With Modified Sensor (Smaller Shape Sensor With BLE) at Home Setting Monitoring a Subject While Partner in Bed
Accuracy evaluation of EarlySense device, a smaller shape sensor with BLE connection to processing unit (HUB)) for use while two people are in bed ("Home Use" scenario) The EarlySense device is intended for continuous…
- Trial name
- NCT05237518
- Testing
- EarlySense Noomi system
- Volunteers
- 36 people, healthy volunteers welcome
- Sponsor
- EarlySense Ltd.
[Trial of device that is not approved or cleared by the U.S. FDA]
- Trial name
- NCT05670210
- Sponsor
- [Redacted]
Opioid Overdose, Opioid-use Disorder
User Acceptability of a Device-Based Opioid Overdose Intervention
This pilot study evaluates the needs of opioid users for a device-based intervention for opioid overdoses. The results of this one-time short questionnaire will inform development of a novel naloxone delivery device.
- Conditions
- Opioid Overdose, Opioid-use Disorder, Substance Use Disorders
- Trial name
- NCT04530591
- Testing
- Survey, Interview
- Where
- United States
- Volunteers
- 97 people
- Sponsor
- University of Pennsylvania
[Trial of device that is not approved or cleared by the U.S. FDA]
- Trial name
- NCT00788437
- Sponsor
- [Redacted]
Improvement of Abdomen Appearance
Effect of the BTL-899 Therapy for Non-invasive Lipolysis and Circumference Reduction of Abdomen When Compared to a Sham Treatment
The study is a prospective single-blinded two-arms study that includes three treatment procedures and four follow-up visits
- Trial name
- NCT04000945
- Testing
- BTL-899
- Where
- Bulgaria
- Volunteers
- 60 people, healthy volunteers welcome
- Sponsor
- BTL Industries Ltd.
Pneumonia
A Study to Determine the Correct Dose of Amikacin Which is Delivered Directly to the Lungs of Ventilated Patients as an Aerosol Via an Investigational Device Called the Pulmonary Delivery Device System (PDDS)
This study is part of a research program too see if amikacin delivered as an aerosol directly to the lungs in combination with IV antibiotic therapy can help intubated patients with gram-negative pneumonia get better faster than…
- Trial name
- NCT01004445
- Testing
- Amikacin (BAY41-6551)
- Where
- 20 sites in United States, France and 1 more
- Volunteers
- 69 people
- Sponsor
- Bayer
Cancer of Pancreas, Cancer of Pelvis
Daily Imaging, Target Identification, and Simulated Computed Tomography-Based Stereotactic Adaptive Radiotherapy Workflow in a Novel Ring Gantry Radiotherapy Device
The investigators propose here to evaluate the feasibility of a novel cone-beam CT (CBCT)-guided online adaptive radiotherapy (ART) workflow on the Halcyon device.
- Conditions
- Cancer of Pancreas, Cancer of Pelvis, Cancer of Abdomen, Cancer of Thorax
- Trial name
- NCT04008537
- Testing
- Ring gantry kV-CBCT combined with linear accelerator
- Where
- United States
- Volunteers
- 37 people
- Sponsor
- Washington University School of Medicine
Premature Ejaculation, Masturbation
Efficacy of App and Electronic Device in the Treatment of Premature Ejaculation
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…
- Conditions
- Premature Ejaculation, Masturbation, Medical Device
- Trial name
- NCT04012437
- Testing
- Sphincter Control Training (SCT)
- Where
- Spain
- Volunteers
- 40 people
- Sponsor
- Instituto Sexológico Murciano
Percutaneous Intervention Via Femoral Artery
Star-Close Versus Angio-Seal for Femoral Artery Hemostasis
This study was designed to evaluate the efficacy and safety of Starclose (Abbott Vascular Devices) for femoral access site closure in patients undergoing PCI compared to Angio-Seal STS Plus (St. Jude Medical).
- Trial name
- CLOSE (NCT00590356)
- Testing
- StarClose®, AngioSeal®
- Where
- South Korea
- Sponsor
- Seung-Jung Park
Amputation, Amputation; Traumatic, Hand
Evaluation of Myoelectric Implantable Recording Array (MIRA) in Participants With Transradial Amputation
The purpose of this research study is to see how well a new type of myoelectric prosthesis works. A myoelectric prosthesis is a robotic limb for amputees that is controlled by sensing the activity of muscles in the body above the…
- Trial name
- MIRA (NCT05768802)
- Testing
- Myoelectric Implantable Recording Array (MIRA)
- Where
- United States
- Volunteers
- 5 people
- Sponsor
- Boninger, Michael, MD
Stroke
Upper Limb Robotic Rehabilitation During COVID-19 Outbreak
The COVID-19 outbreak requires a rapid re-shaping of the entire organization of the rehabilitation services. This includes the design and planning of appropriate rehabilitation settings, intervention and logistics for organizing…
- Trial name
- NCT04392453
- Testing
- Robotic therapy
- Where
- Italy
- Volunteers
- 22 people
- Sponsor
- Fondazione Don Carlo Gnocchi ETS
Infiltration of Peripheral IV Therapy
ivWatch Model 400: Device Validation for Infiltrated Tissues
A single arm trial consisting of 70 adult volunteers to assess the safety and efficacy of the ivWatch Model 400 when observing infiltrated tissues at common sites for peripheral IV therapy.
- Trial name
- NCT02123745
- Testing
- The ivWatch Model 400
- Where
- United States
- Volunteers
- 71 people, healthy volunteers welcome
- Sponsor
- ivWatch, LLC
Cutaneous Allergy, Diabetes Mellitus, Type 1
Skin Tolerance of Medical Devices for Diabetes Monitoring and Treatment in Children With Type 1 Diabetes
In view of the emergence over the last few years of adverse skin reactions caused by diabetes monitoring and treatment devices, which have become essential to the optimal management of these patients, it is necessary to determine…
- Conditions
- Cutaneous Allergy, Diabetes Mellitus, Type 1, Atopic Disorders
- Trial name
- NCT05932953
- Testing
- questionary
- Where
- France
- Volunteers
- 400 people
- Sponsor
- Central Hospital, Nancy, France
Chickenpox
Open Clinical Investigation to Evaluate the Effectiveness and Safety of a Topical Medical Device.
The primary endpoint is the change of the itching score after 3 days of the product use in comparison to the basal value.
- Trial name
- NCT05732337
- Testing
- Poxclin Coolmousse
- Where
- Poland
- Volunteers
- 28 people, healthy volunteers welcome
- Sponsor
- Karo Pharma AB
Digital Health Intervention, Remote Consultation, Teleconsultation
Evaluation and Implementation of Digital Health Ecosystem in Academic Health Center
Mobile health technologies, such as smartwatches, wearable sensors, and digital applications, have the potential to support healthier lifestyles and improve the management of health conditions.
- Conditions
- Digital Health Intervention, Remote Consultation, Teleconsultation, Lifestyle Factors, Stress
- Trial name
- e-IDEA (NCT07831837)
- Testing
- Integrated Digital Health Ecosystem, Usual Primary Care
- Where
- 2 sites in Canada
- Volunteers
- 60 people, healthy volunteers welcome
- Sponsor
- Laval University
Pulmonary Neoplasm
Impact of Different Lung Isolation Devices on Pharyngolaryngeal Injuries After Pulmonary Resection
The goal of this clinical trial is to assess the impact of laryngeal mask combined with visual bronchial blocker on pharyngolaryngeal injury after pulmonary resection in patients with pulmonary nodules.
- Trial name
- PLIAP (NCT07117539)
- Testing
- visual bronchial blocker (VBB), double-lumen endotracheal tube (DLT)
- Where
- 3 sites in China
- Volunteers
- 270 people
- Sponsor
- Tingting Li
[Trial of device that is not approved or cleared by the U.S. FDA]
- Trial name
- NCT00758875
- Sponsor
- [Redacted]
Breathing, Mouth, Lung Function Decreased
Evaluating the Use of a Device Called Impulse Oscillometry in Participants With Vocal Cord Disorders or Asthma
This study will determine if airway resistance to airflow and pressure, measured by Impulse Oscillometry, is impacted in subjects with vocal cord disorders and whether these measurements are different when compared to subjects…
- Conditions
- Breathing, Mouth, Lung Function Decreased, Vocal Cord Dysfunction, Laryngeal Obstruction
- Trial name
- NCT05246930
- Testing
- Impulse Oscillometer
- Where
- United States
- Volunteers
- 43 people
- Sponsor
- University of Rochester
Intracranial Aneurysm
Nomogram for Predicting In-stent Stenosis After Pipeline Embolization Device Treatment in Patients With Intracranial Aneurysm
Intracranial aneurysms (IAs) are the primary cause of non-traumatic subarachnoid hemorrhage with high morbidity and mortality. Flow diverters, such as pipeline embolization devices (PEDs), are among the most effective methods for…
- Trial name
- PED-ISS (NCT06715930)
- Testing
- Interventional treatment
- Where
- China
- Volunteers
- 1,500 people
- Sponsor
- Beijing Tiantan Hospital