Clinical trials: VALİDİTY
Intracranial Hypertension, Abnormality of Intracranial Pressure
Validation of Non-Invasive Intracranial Pressure (ICP) Monitoring Device
For purposes of validation, this study compares intracranial pressure measurements obtained with a novel self-calibrating, non-invasive, intracranial pressure measuring (ICP) device, with the values obtained from (a) patients in…
- Trial name
- NCT03865576
- Testing
- Non-invasive ICP measurement
- Where
- 4 sites in United States
- Volunteers
- 80 people
- Sponsor
- Boston Neurosciences
Nutrition Poor
Validation of a Nutrient Profiling System for Reformulation
The objectives of the study are to assess the validity of Nestlé reformulation criteria in two national dietary surveys: the US NHANES 2011, and the French INCA2 2006-07.
- Trial name
- NCT03411603
- Testing
- Diet and socio-demographic questionnaires
- Volunteers
- 6,991 people, healthy volunteers welcome
- Sponsor
- Société des Produits Nestlé (SPN)
Uterine Fibroids, Uterine Leiomyomas
MR Guided Focused Ultrasound Surgery in the Treatment of Uterine Fibroids: Software V4.2 Validation
The goal of this study is to validate the new ExAblate Application software V4.2 by developing additional data that shows the safety of this treatment.
- Trial name
- NCT00295217
- Testing
- ExAblate 2000
- Where
- 4 sites in United States
- Volunteers
- 15 people, healthy volunteers welcome
- Sponsor
- InSightec
Atrial Fibrillation
Withings ECG-app Study
The aim of the study is to evaluate the performance of Withings HWA10 with embedded Withings ECG-app in the automatic detection of atrial fibrillation
- Trial name
- NCT05316350
- Testing
- Electrocardiogram recording
- Where
- 10 sites in United States, France
- Volunteers
- 685 people
- Sponsor
- Withings
Lung Diseases, Lung Cancer Screening
Validation of the SPOT-MAS Lung Test Using Circulating Tumor DNA for the Detection of Lung Cancer
This is an observational clinical trial, aiming to evaluate the efficacy of the SPOTMAS LUNG (SML) test compared to Low dose CTScan (LDCT)/None contrast CTScan (NCCT) in two distinct risk populations: Cohort A: To demonstrate…
- Trial name
- NCT07126626
- Where
- Vietnam
- Volunteers
- 1,184 people
- Sponsor
- Gene Solutions
Pelvic Organ Prolapse
Validation of Transvaginal Tactile Imaging
The purpose of this study is to validate safety and effectiveness in assessment of the female pelvic floor tissue, and, assess the ability of Vaginal Tactile Imager (VTI) to detect early prolapse conditions and characterize the…
- Trial name
- VTI-03 (NCT01491334)
- Where
- 2 sites in United States
- Volunteers
- 158 people, healthy volunteers welcome
- Sponsor
- Artann Laboratories
Healthy
Desaturation Validation of INVSENSOR00009
This study is designed to measure the trending accuracy of a noninvasive measurement of cerebral oxygen saturation. One Large sensor (adult sensor) and one INVSENSOR00009 will be placed on the subject's forehead.
- Trial name
- NCT03396835
- Testing
- INVSENSOR00009
- Where
- United States
- Volunteers
- 16 people, healthy volunteers welcome
- Sponsor
- Masimo Corporation
Allergy, Allergic Asthma
Analytical Validation of the abioSCOPE Device With an IgE Test Panel: Point-of-Care Precision, Sample Type Comparison and Method Correlation
This is a multicenter, prospective, observational study to evaluate the analytical performance of the Abionic IgE Multi-Allergen Test Panel on the abioSCOPE® device in a U.S.
- Conditions
- Allergy, Allergic Asthma, Allergy to Cats, Allergy to House Dust
- Trial name
- NCT04401631
- Testing
- Blood Collection
- Where
- 3 sites in United States
- Volunteers
- healthy volunteers welcome
- Sponsor
- Abionic SA
COVID-19, Sars-CoV-2 Infection
This Trial is a Clinical Performance Validation Study That Will Evaluate the Clinical Agreement of the Sky Medical™ Rapid Antigen Test Comparing the Antigen Rapid Test to RT-PCR
Prospective study that will evaluate the clinical agreement of the Sky Medical™ Rapid Antigen Test compared to SARS-CoV-2 RT-PCR.
- Trial name
- NCT05491993
- Testing
- Sky Medical™ Rapid Antigen Test
- Where
- United States
- Volunteers
- 200 people
- Sponsor
- Sky Medical Supplies & Equipments, LLC
Healthy Population, Chronic Disease
Verily Clinical Study Watch Analytical Validation Study
This study is designed to evaluate the performance of the Verily Clinical Study Watch for the quantification of participants' movement and pulse rate when the wearer is at rest.
- Trial name
- NCT05534477
- Testing
- Verily Clinical Study Watch, Vivalink ECG Patch, Modus StepWatch 4
- Where
- United States
- Volunteers
- 100 people, healthy volunteers welcome
- Sponsor
- Verily Life Sciences LLC
Complete Questionnaires Following TKR Surgery
Development of a New Patient Reported Outcome Measure (PROM) to Assess Patient's Emotional Wellbeing, and Perceptions of Total Knee Replacement Surgery for the Treatment of Knee Arthritis
Development of a new Patient Reported Outcome Measure (PROM) to assess patient's emotional wellbeing, and perceptions of Total Knee Replacement surgery for the treatment of knee arthritis.
- Trial name
- SYNC01- P4 (NCT06585267)
- Where
- United Kingdom
- Volunteers
- 167 people
- Sponsor
- Invibio Ltd
Steatoblepharon
Live Validation of the Lower Eyelid Steatoblepharon Severity (LESS) Scale
This observational study will test the inter-rater and test-retest reliability of the LESS scale in a live context.
- Trial name
- NCT02609763
- Volunteers
- 100 people, healthy volunteers welcome
- Sponsor
- Topokine Therapeutics, Inc.
Low Back Pain, Neck Pain
Wearable Spine Assessment in Adults With and Without Low Back or Neck Pain
This is a single-site, prospective, observational, single-visit feasibility and validity study. Adult participants with and without low back or neck pain will be screened, consented, and enrolled to undergo a structured…
- Trial name
- AxiSens-01 (NCT07643207)
- Where
- United States
- Volunteers
- 5 people, healthy volunteers welcome
- Sponsor
- Ashkan Vaziri
Establish Normative pH Values in Neonates
Product Validation Study of RightSpot Infant pH Indicator for Rapid Bedside Verification of Proper Nasogastric (NG) Tube Placement in Newborn Intensive Care (NICU) Patients
Objectives: 1. To validate the accuracy of pH measurements of gastric fluid by comparing the readings from the RightSpot Infant pH Indicator to a standard clinically approved pH monitor 2.
- Trial name
- NCT02279264
- Testing
- RightSpot Infant pH Indicator
- Where
- United States
- Volunteers
- 40 people
- Sponsor
- RightBio Metrics
Osteoporosis, Osteopenia
Bone UltraSonic Scanner (BUSS): Validation Study
The aim of clinical study is to assess effectiveness of Bone UltraSonic Scanner (BUSS) versus densitometry (DXA) in osteoporosis detection.
- Trial name
- NCT01439139
- Where
- United States
- Volunteers
- 130 people, healthy volunteers welcome
- Sponsor
- Artann Laboratories
Hypoxia
SpO2 Hypoxia Accuracy Validation Study
The primary objective of this study is to evaluate the % oxygen saturation by pulse oximetry accuracy of a combined pulse oximetry system which consists of a Nonin sensor ), an adaptor cable, and an oximetry system during…
- Trial name
- NCT03348189
- Testing
- Pulse Oximeter
- Where
- United States
- Volunteers
- 12 people, healthy volunteers welcome
- Sponsor
- Nonin Medical, Inc
Febrile, Healthy
The Clinical Performance Validation of Electronic Thermometer and Infrared Thermometers
Geon Corporation develops ear thermometers and forehead thermometers that use infrared measurement technology to measure human body temperature. This study verify the accuracy and repeatability of investigational devices.
- Trial name
- NCT06353490
- Testing
- Infrared Forehead Thermometer (GE-TF03), Infrared Ear Thermometer (GE-TE06), Electronic Thermometer (MT-B321FB)
- Where
- 2 sites in Taiwan
- Volunteers
- 150 people, healthy volunteers welcome
- Sponsor
- Geon Corporation
Alzheimer's Disease, Amnestic Mild Cognitive Impairment
[18F]MK-6240 Positron Emission Tomography (PET) Tracer First-in-Human Validation Study (MK-6240-001)
This 2-part, open-label study was designed to investigate the safety, tolerability, and efficacy of [18F]MK-6240, a Positron Emission Tomography (PET) imaging agent, for the quantification of neurofibrillary tangle (NFT)…
- Trial name
- NCT02562989
- Testing
- [18F]MK-6240, ~185 MBq, [18F]MK-6240, ~160 MBq
- Volunteers
- 13 people, healthy volunteers welcome
- Sponsor
- Merck Sharp & Dohme LLC
Glioma, Malignant, Computer-Assisted
Radiomics-Based Visualization and Quantitative Validation of IDH1 Heterogeneity in Gliomas
The goal of this clinical trail is to non-invasively visualise and quantitatively validate an radiomics model of genetic heterogeneity in adult patients with diffuse glioma to help clinicians better guide surgical resection and…
- Trial name
- NCT05969691
- Testing
- Validation of IDH1 mutations from the radiomics model
- Where
- China
- Volunteers
- 18 people
- Sponsor
- Mingge LLC
Anemia
Spot-Check Noninvasive Hemoglobin (SpHb) Clinical Validation of INVSENSOR00026
The primary objective of this clinical investigation is to evaluate the accuracy of using Masimo's INVSENSOR00026 Pulse CO-Oximeter and Sensor to measure hemoglobin, as compared to hemoglobin measurements obtained from various…
- Trial name
- NCT03610269
- Testing
- INVSENSOR00026 (Pulse CO-Oximeter and sensor)
- Where
- United States
- Volunteers
- 143 people, healthy volunteers welcome
- Sponsor
- Masimo Corporation