Clinical trials: Device
Oncology, Medical, Hematologic Disease
Safety of Catheter Lock With or Without Heparin in Implanted Central Venous Catheters
Long-term central venous access devices are considered as safe for the administration of medication as chemotherapy, but are also used for blood sampling.
- Trial name
- NCT00994136
- Testing
- normal saline
- Where
- Belgium
- Volunteers
- 1,100 people
- Sponsor
- Universitaire Ziekenhuizen KU Leuven
Needle Phobia, Virtual Reality
Use of Augmented Reality and Virtual Reality During Cognitive Behavioral Therapy for Needle Phobia
This case series study seeks to evaluate the use of a Spatial Computing Device and Augmented Reality (AR) and Virtual Reality (VR) as an exposure therapy modality for children and adolescents with needle and…
- Conditions
- Needle Phobia, Virtual Reality, Cognitive Behavior Treatment
- Trial name
- SNAC (NCT07042074)
- Testing
- Mixed reality (XR) Exposure Therapy
- Where
- United States
- Volunteers
- 20 people
- Sponsor
- Stanford University
Blood Pressure
Validation of a Noninvasive Automated Blood Pressure Device
The investigator's objective is to validate the novel automated blood pressure device against the requirements set forth in the AAMI_ISO 81060-2:2010 standard in voluntarily consented study participants.
- Trial name
- NCT03566888
- Testing
- Blood pressure assessment
- Where
- United States
- Volunteers
- 85 people, healthy volunteers welcome
- Sponsor
- University of Southern California
Dehydration
Hydration Status Evaluation of Dehydrated Children With Experimental Devices
A pediatric study in collaboration with Boston Children's Hospital to review the performance of two novel hydration status measurement devices against standard clinical assessment methods, through repeated measurement of…
- Trial name
- NCT02960789
- Testing
- Formalized clinical assessment of hydration status, Take a measurement of body weight on calibrated scales, "RF wristband" hydration status measurement
- Where
- 2 sites in United States
- Volunteers
- 137 people
- Sponsor
- Massachusetts Institute of Technology
Treatment
Pipeline Embolization Device for the Treatment of Intracranial Aneurysms on the Long Term Safety and Efficacy
Since its launch in China in 2014, Pipeline Embolization Device (PED) has been widely used in the treatment of intracranial aneurysms.
- Trial name
- NCT06456697
- Where
- China
- Volunteers
- 482 people
- Sponsor
- Xuanwu Hospital, Beijing
Diabetes Mellitus, Polyneuropathies
Cost-effectiveness of In-shoe Pressure Measurement for Therapeutic Shoes
The purpose of this study is determine whether the use of plantar pressure measurements in the production of customized therapeutic footwear for patients with diabetes and a history of foot ulceration results in lower production…
- Trial name
- NCT02061059
- Testing
- block 1, block 2, standard
- Where
- 2 sites in Netherlands
- Volunteers
- 40 people
- Sponsor
- Maastricht University
PFO - Patent Foramen Ovale, ASD - Atrial Septal Defect
Trevisio Post-Approval Study
A single-arm, non-randomized, multi-center clinical study of the Amplatzer™ Trevisio™ Intravascular Delivery System for facilitating percutaneous, transcatheter implantation of the Amplatzer™ Occluder Devices.
- Conditions
- PFO - Patent Foramen Ovale, ASD - Atrial Septal Defect, VSD - Muscular Ventricular Septal Defect, PIVSD - Post Infarct Muscular Ventricular Septal Defect
- Trial name
- TrevisioPAS (NCT04433520)
- Testing
- Amplatzer™ Trevisio™ Intravascular Delivery System using Amplatzer PFO Occluder, ASO or Amplatzer Cribriform Occluder, Amplatzer™ Trevisio™ Intravascular Delivery System using Amplatzer Muscular VSD Occluder or Amplatzer Post-Infarct Muscular VSD Occluder
- Where
- 22 sites in France, Germany and 5 more
- Volunteers
- 254 people
- Sponsor
- Abbott Medical Devices
Anesthesia
Hand Held Nitrous Oxide Delivery Device
To study the safety and efficacy of Hand Held Nitrous. A device that delivers 120 seconds of up to 72% nitrous oxide and ambient air.
- Trial name
- HHN (NCT02119403)
- Testing
- There are no other inteventions.
- Where
- 2 sites in United States
- Volunteers
- 250 people
- Sponsor
- Strata Medical Innovations
Light Fluorescence Device
Clinical Effectiveness of(VistaProof)in Comparison With ICDAS-II & Histological Validation for Detecting Occlusal Caries
a diagnostic accuracy study control trial is to be held to evaluate the Clinical performance of quantitative light fluorescence based device (Vistacam Proof) in comparison with the visual examination and histological validation…
- Trial name
- NCT03940170
- Testing
- vistacam proof, ICDASII, fissurotomy
- Where
- Egypt
- Volunteers
- 24 people
- Sponsor
- Mohamed samy El-sayed
Influenza A, Influenza B
Detection of Influenza A, Influenza B, and RSV Using the Liat™ Assays on the Liat™ Analyzer
The objective of this study is to evaluate the clinical sensitivity and specificity of the Liat™ Influenza A/B \& RSV Assay and the Liat™ Influenza A/B Assay when used on the Liat Analyzer to detect the presence or absence of…
- Conditions
- Influenza A, Influenza B, Respiratory Syncytial Virus (RSV)
- Trial name
- NCT02067286
- Where
- 8 sites in United States
- Volunteers
- 1,642 people
- Sponsor
- IQuum, Inc.
Laceration, Skin Wound
Comparison of microMend® Devices to Sutures in Closing Lacerations in Children
This study will gather information on the use of microMend® to repair lacerations in children and compare the efficacy of microMend® to sutures for laceration repair.
- Conditions
- Laceration, Skin Wound, Wound Heal
- Trial name
- NCT04557761
- Testing
- microMend®, Closure with Sutures
- Where
- United States
- Volunteers
- 30 people
- Sponsor
- Children's Hospital of Orange County
Cystic Fibrosis, Venous Thrombosis
Cystic Fibrosis and Totally Implantable Vascular Access Devices
The purpose of this study is to evaluate the incidence of venous thrombosis occurring on totally implantable vascular access devices in cystic fibrosis patients who need a new device (it can be the first one or a subsequent one)…
- Trial name
- RITHM (NCT00244270)
- Testing
- totally implantable vascular access device
- Volunteers
- 97 people
- Sponsor
- Assistance Publique - Hôpitaux de Paris
Efficacy of a Noise Reduction Program, Surgical Complications
Prospective Trial on Noise Reduction in Surgical Operating Theaters
Aim of Study: Adverse effects from noise pollution in operation theatres have been throughly demonstrated. We assessed the impact of a noise reduction program in paediatric surgery.
- Conditions
- Efficacy of a Noise Reduction Program, Surgical Complications, Sound Pressures in the Operating Theatre
- Trial name
- NCT01612754
- Testing
- Noise reduction work place rules, Presence of an examiner in the concerned theatre
- Where
- Germany
- Volunteers
- 16 people, healthy volunteers welcome
- Sponsor
- Hannover Medical School
"Lost" IUD
Anesthetic Efficacy of Intrauterine Lidocaine for Removal of a "Lost" Intrauterine Device
Objective: To evaluate the efficacy of intrauterine lidocaine instillation in reducing patient discomfort during the removal of a "lost" intrauterine device (IUD).
- Trial name
- NCT00308841
- Testing
- Lidocaine (drug)
- Where
- Turkey (Türkiye)
- Sponsor
- Suleyman Demirel University
Hemiparesis, Paraparesis
Immediate Effects On Gait and Spasticity After The Use Of Passive Kinesiotherapy Equipment In The Lower Limbs Of Neurological Patients
Undergo assessment of muscle tone (Ashworth Scale), gait (BAIOBIT) and risk of falling (Timed Up and Go) before using the device; Use the device on the spastic lower limb(s) for 30 minutes; Go through the same assessment carried…
- Conditions
- Hemiparesis, Paraparesis, Tetraparesis, Cerebral Palsy
- Trial name
- NCT06696040
- Testing
- Passive mobilization using a device
- Where
- Brazil
- Volunteers
- 80 people
- Sponsor
- Fernanda Trubian
Fracture Arm, Fracture Leg
Accuro XV Ultrasound Imaging System for BoneEnhance and Fracture Detection Algorithms
The Accuro XV is a cart-based, bedside ultrasound instrument that incorporates new signal processing-based technologies for enhanced bone and soft-tissue imaging.
- Conditions
- Fracture Arm, Fracture Leg, Wrist Injury, Ankle Injury
- Trial name
- NCT07853768
- Testing
- Accuro XV Ultrasound Imaging System
- Where
- 10 sites in United States
- Volunteers
- 25,000 people
- Sponsor
- Rivanna Medical, Inc.
Jaundice
Value of Transcutaneous Bilirubin Devices
The goal of this observational study is to compare the value of transcutaneous bilirubin devices versus serum bilirubin in jaundiced neonates
- Trial name
- NCT06232174
- Where
- Egypt
- Volunteers
- 80 people
- Sponsor
- Assiut University
Congenital Heart Disease
RAPID: a Comparison Study of a Novel Ultrasound Device of Automated Congenital Heart Imaging
The RAPID ultrasound is a portable imaging device that captures a one point image from the subcostal region of the heart. The device is set on the patient's chest and captures the image in \<1 minute.
- Trial name
- NCT06281639
- Testing
- RAPID
- Where
- United States
- Volunteers
- 22 people
- Sponsor
- University of Minnesota
Vital Signs
Detection of Deterioration by SNAP40 Versus Standard Monitoring in the ED
In recent years there has been increasing focus on the earlier detection of deterioration in the clinical condition of hospital patients with the aim of instigating earlier treatment to reverse this deterioration and prevent…
- Trial name
- SNAP40ED (NCT03179267)
- Testing
- SNAP40
- Where
- United Kingdom
- Volunteers
- 250 people
- Sponsor
- NHS Lothian
Hemiplegia, Cerebral Palsy
Motus Nova Foot Device for Patients With Hemiplegia
Individuals with hemiplegia commonly demonstrate gait deviations such as difficulties with heel strike at initial contact, foot drop in swing, asymmetrical limb loading, muscle activation, and balance impairments.
- Conditions
- Hemiplegia, Cerebral Palsy, Hemiplegic Cerebral Palsy
- Trial name
- NCT07754773
- Testing
- Motus Nova Foot
- Where
- United States
- Volunteers
- 5 people
- Sponsor
- MultiCare Health System Research Institute
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