Clinical trials: Device
Device Validation of In-vivo Performance
Trima Non-DEHP Leukoreduced Red Blood Cell In Vivo Recovery Study
This is an in vivo 24-hour in-vivo recovery study of leukoreduced red blood cells (RBCs) collected on the Trima Accel System using Non-DEHP disposable sets and stored for 42 days.
- Trial name
- NCT06602804
- Testing
- Trima Accel Auto RBC Collection
- Where
- 2 sites in United States
- Volunteers
- 37 people, healthy volunteers welcome
- Sponsor
- Terumo BCT
LVAD (Left Ventricular Assist Device) Driveline Infection
A Silver Lining in the VAD Sky
The investigators propose to conduct a prospective randomized trail (RCT) of a driveline management protocol. The study will be initiated at UCSF from January 1st 2022 to December 31st 2022 as a pilot to be extended to other…
- Trial name
- LVAD-SilverD (NCT05163392)
- Testing
- Silverlon, Control
- Where
- United States
- Volunteers
- 25 people, healthy volunteers welcome
- Sponsor
- University of California, San Francisco
Alzheimer's Dementia, Neuropsychiatric Symptoms Related to Neurodegenerative Disease
Feasibility of Wearables in Dementia Care in Rural Taiwan
Taiwan is becoming a super-aged society, and more older adults are living with Alzheimer's disease. Many people with Alzheimer's experience behavioral and psychological symptoms, such as agitation, sleep problems, or mood…
- Conditions
- Alzheimer's Dementia, Neuropsychiatric Symptoms Related to Neurodegenerative Disease, Wearable Devices, Caregiver Burden of People With Dementia
- Trial name
- NCT07249918
- Testing
- Re-Timer (light therapy glasses)
- Where
- Taiwan
- Volunteers
- 20 people, healthy volunteers welcome
- Sponsor
- China Medical University Hospital
Ventilator Acquired Pneumonia, Central Line Associated Blood Stream Infections (CLABSI)
Evidence-Based Nursing to Reduce Adverse Events Regarding Ventilator Associated Pneumonia, Pressure Injuries and Central Line Bloodstream Infection in Intensive Care Unit in Bangladesh
Quality of care is crucial for preventing adverse events such as infection in the intensive care units (ICUs). The most common ICU-acquired infections include pneumonia such as Ventilator Associated Pneumonia (VAP), Pressure…
- Conditions
- Ventilator Acquired Pneumonia, Central Line Associated Blood Stream Infections (CLABSI), Pressure Ulcer (PU), Medical Device Related Pressure Ulcer (MDRPU)
- Trial name
- EBP in Nursing (NCT07299799)
- Testing
- Education with EBP, This is a pre- and post- quasi-experimental study.
- Where
- 2 sites in Bangladesh, Japan
- Volunteers
- 272 people, healthy volunteers welcome
- Sponsor
- Hiroshima University
This Study Explores How Young Children Aged 3 to 5 Use Interactive Electronic Devices
Observing 3-5 Year Old Children's Use of Interactive Electronic Devices (IED) in the Family Home to Understand the Context These Devices Are Being Used in, Exploring Whether Socioeconomic Factors or Parent's Own Use of Such Devices Influence the Child's IED Usage.
This study aims to explore the context of how children aged 3-5 use interactive electronic devices like tablets or smartphones in their everyday home environment.
- Trial name
- iKids (NCT07373483)
- Where
- United Kingdom
- Volunteers
- 20 people, healthy volunteers welcome
- Sponsor
- Sheffield Hallam University
MR Multinuclear, Image Quality
MR 7700 Multinuclear Application Clinical Trial
The purpose of this clinical trial is to use the medical magnetic resonance imaging system MR 7700 to perform phosphorus (31P) and sodium (23Na) scanning imaging on the human body, evaluate the image quality of phosphorus (31P)…
- Conditions
- MR Multinuclear, Image Quality, Device Convenience, Device Stability
- Trial name
- NCT07368036
- Testing
- MR Scanning with Phosphorus nucleus + Sodium nucleus
- Volunteers
- 200 people, healthy volunteers welcome
- Sponsor
- Philips Clinical & Medical Affairs Global
Wearable Electronic Devices, Polygenic Risk Score
DELphi Procedure for Developing Recommendations for the Implementation of Wearable Devices and Polygenic Risk Scores
DEL-DIP is a prospective observational study employing a Delphi methodology (at least two online rounds) to elicit and consolidate the views of an expert panel within the INNOPREV project.
- Conditions
- Wearable Electronic Devices, Polygenic Risk Score, CVD - Cardiovascular Disease, Primary Prevention
- Trial name
- DEL-DIP (NCT07358481)
- Where
- Italy
- Volunteers
- 10 people, healthy volunteers welcome
- Sponsor
- Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Back Pain, Exoskeleton Device
Effects of Wearable Passive Back Support Suit on Back Pain in Caregivers
The physical demands of patient transport, including lifting and transferring patients, are significant contributors to the high risk of musculoskeletal disorders.
- Trial name
- back pain (NCT07333157)
- Testing
- wearable passive back support suit, traditional lumbosacral orthosis
- Where
- South Korea
- Volunteers
- 30 people, healthy volunteers welcome
- Sponsor
- Samsung Medical Center
Urinary Catheterization, Device
Positioning Device for Female Urinary Catheterization
In female patients, the dorsal recumbent position is required to visualize the urethral meatus. In female patients, direct visualization of the urethral meatus after providing a suitable position is very important for successful…
- Conditions
- Urinary Catheterization, Device, Nursing, Positioning (Prone, Right Lateral and Semi-Elevated Supine Position)
- Trial name
- NCT07327671
- Testing
- dorsal recumbent positioning device
- Where
- Turkey (Türkiye)
- Volunteers
- 60 people, healthy volunteers welcome
- Sponsor
- Saglik Bilimleri Universitesi Gulhane Tip Fakultesi
Device Replacement
A Comparative Study of Portable Patch-type Carotid Ultrasound CADFlow and Desktop Ultrasound Machines
observational study The purpose of this observational study is to clarify the consistency, accuracy, and reproducibility of portable patch carotid ultrasound (CADFlow) compared to desktop ultrasound machines in detecting cardiac…
- Trial name
- NCT07197411
- Testing
- Evaluating the Consistency and Accuracy of Two Devices in Monitoring Hemodynamic Parameters, Hemodynamic monitoring
- Where
- China
- Volunteers
- 140 people, healthy volunteers welcome
- Sponsor
- Xuzhou Medical University Affiliated Suqian Hospital
Intrauterine Device
Can Uterocervical Angle Predict the Displacement of Copper Intrauterine Devices (T-Cu 380A)
The investigators conducted a case-control study between December 2020-June 2021 at Istanbul Health Sciences University Kanuni Sultan Suleyman Training and Research Hospital family planning outpatient clinics.
- Trial name
- NCT05556421
- Testing
- uterocervical angle
- Where
- Turkey (Türkiye)
- Volunteers
- 123 people, healthy volunteers welcome
- Sponsor
- Kanuni Sultan Suleyman Training and Research Hospital
Contraception, Intrauterine Device
Structured Contraceptive Counseling During Pregnancy
Unintended pregnancy is common among women of fertile age, and also among those who have recently given birth. A Swedish study has shown that about 7.7% experience a new pregnancy, and that 2.5% will have an abortion between…
- Conditions
- Contraception, Intrauterine Device, Contraceptive Implant, Long-acting Reversible Contraception
- Trial name
- NCT05550064
- Testing
- Structured contraceptive counseling
- Where
- 4 sites in Sweden
- Volunteers
- 160 people, healthy volunteers welcome
- Sponsor
- Dalarna University
Orthotic Devices
Boutonniere Deformity Effectiveness of Thermoplastic and Fabricated Orthoses
The goal of this study is to present the author's thumb orthosis with a butonier deformity and its effect on hand function, strength, dexterity and pain levels in relation to patients wearing factory-made orthopedic supplies.
- Trial name
- NCT06267469
- Testing
- Thermoplastic orthosis
- Where
- 2 sites in Poland
- Volunteers
- 60 people, healthy volunteers welcome
- Sponsor
- Magdalena Kolasińska
Evaluation of IUD Position Six Weeks After Insertion, Intrauterine Device Placement and Displacement
Transvaginal Three-Dimensional Ultrasound for Evaluation of Intrauterine Device Position Six Weeks After Insertion
This study aims to evaluate the position of intrauterine devices (IUDs) six weeks after insertion using transvaginal three-dimensional (3D) ultrasound.
- Trial name
- NCT07138248
- Testing
- 2D Transvaginal Ultrasound
- Where
- Egypt
- Volunteers
- 138 people, healthy volunteers welcome
- Sponsor
- Assiut University
Device Safety
Adaptive Study to Assess the Safety and Functioning of Motiva Devices on Minimally Invasive Gluteal Augmentation
The objective of this clinical trial is to assess the initial performance and safety of Motiva® Ergonomix2® Diamond®, Motiva Injector®, Motiva® Inflatable Balloon, Motiva® Reusable Channel Dissector, and Motiva® GEM Channel…
- Trial name
- GEM (NCT07135011)
- Testing
- Primary gluteal enhancement
- Where
- Costa Rica
- Volunteers
- 120 people, healthy volunteers welcome
- Sponsor
- Establishment Labs
Endometrial Biopsy, Intrauterine Devices
Methoxyflurane for IUD Insertion and Endometrial Biopsy
The aim of this study is to determine if 3ml of inhaled Methoxyflurane, in the form of a Penthrox inhaler, reduces pain during IUD insertion and/or endometrial biopsy. The proposed study is a double-blind, placebo-controlled RCT.
- Trial name
- NCT07046572
- Testing
- Methoxyflurane - Penthrox
- Where
- Canada
- Volunteers
- 174 people, healthy volunteers welcome
- Sponsor
- Mount Sinai Hospital, Canada
Exoskeleton Device
Evaluation of Trunk Assistance Exoskeleton
The goal of this interventional study is to evaluate the effect of three different designs of trunk assistance exoskeletons on cumulative lumbar load, trunk extensors' muscular fatigue and comfort in healthy volunteers.
- Trial name
- NCT07084974
- Testing
- Adjustment and practice session, No trunk assistance, Uplift Lite exoskeleton
- Where
- Canada
- Volunteers
- 20 people, healthy volunteers welcome
- Sponsor
- TOPMED
Low-immersion (Mobile Device), High-immersion (Head Mounted Display)
Developing a Virtual Reality Training Tool for Exposure Therapy: Simulated Exposure Trainer (SET)
The goal of this study is to develop a targeted virtual training program (Simulated Exposure Trainer; SET) for exposure therapy.
- Trial name
- SET-VR (NCT06706245)
- Testing
- SET-VR (computer), SET-VR (headset)
- Where
- United States
- Volunteers
- 42 people, healthy volunteers welcome
- Sponsor
- Bradley Hospital
Intrauterine Device (IUD), Abnormal Uterine Bleeding
Suction Cervical Stabilizer Compared to Standard Tenaculum for Intrauterine Procedures
To evaluate patient-reported pain, bleeding, and device efficiency along with provider satisfaction and ease of use between intrauterine procedures employing a suction cervical stabilizer (new device, FDA approved, atraumatic) or…
- Trial name
- NCT06193590
- Testing
- Carevix, Tenaculum
- Where
- United States
- Volunteers
- 73 people, healthy volunteers welcome
- Sponsor
- Indiana University
Medical Device Site Injury
The Effects of PechaKucha Presentation About Medical Device-Related Pressure Injuries
In the literature, no research has been found examining the knowledge and attitudes of students regarding medical device related pressure injury education given using the PK method.
- Trial name
- NCT06650982
- Testing
- Pecha Kucha presentation on MDPRI
- Where
- Turkey (Türkiye)
- Volunteers
- 120 people, healthy volunteers welcome
- Sponsor
- MAİDE YEŞİLYURT