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NCT ID: NCT05525026 Completed - Wrinkle Clinical Trials

Evaluation of Safety and Efficacy of the BTL-785F Device for Non-invasive Facial Remodeling

Start date: December 8, 2021
Phase: N/A
Study type: Interventional

This study will evaluate the clinical safety and the performance of the BTL-785F system equipped with the BTL-785-7 applicator for non-invasive facial remodeling.

NCT ID: NCT05524948 Completed - Halitosis Clinical Trials

A Clinical Study to Examine the Effects of an Experimental Toothpaste Compared to a Regular Fluoride Toothpaste on Breath Odor in a Population With Gingivitis

Start date: September 26, 2022
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate the efficacy of an experimental dentifrice, containing 0.454 percent (%) stannous fluoride and 0.3% zinc chloride, to reduce oral malodor, compared to a marketed regular fluoride dentifrice after 3 weeks twice daily brushing in a population of clinically diagnosed gingivitis.

NCT ID: NCT05524766 Completed - Wrinkle Clinical Trials

BTL-785F Device for Non-invasive Facial Rejuvenation in Patients Injected With Botulinum Toxin

Start date: July 6, 2022
Phase: N/A
Study type: Interventional

This study will evaluate the clinical safety and the efficacy of the BTL-785F system equipped with the BTL-785-7 applicator for non-invasive facial treatment in patients injected with botulinum toxin. The aim is to investigate the improvement of overall facial appearance and muscle tone.

NCT ID: NCT05524753 Completed - Clinical trials for Autism Spectrum Disorder

Active Ingredients & Efficacy of Aquatic Therapy for Autistic Children

Start date: August 4, 2022
Phase: N/A
Study type: Interventional

Accidental drowning is the number one cause of death in children with autism spectrum disorders (ASD) and highlights the critical need for swim lessons and water safety training for this population. Our team has developed and tested an innovative, occupational therapy (OT) based aquatic program - AquOTic - that provides preliminary support for the use of an individualized swim skills training intervention in children with ASD. The AquOTic program uses a combination of sensory, motor learning, and behavioral approaches to improve water safety and swim skills. In this study, we will use a randomized control trial design to identify the efficacy of the AquOTic intervention to improve swim performance in children with ASD.

NCT ID: NCT05524662 Completed - Wrinkle Clinical Trials

Clinical and Histological Evaluation of BTL-785F Device for Non-invasive Treatment of Face

Start date: June 15, 2022
Phase: N/A
Study type: Interventional

This study will evaluate the clinical efficacy, safety and the performance of the BTL-785-7 applicator of the BTL-785F system for non-invasive treatment of facial wrinkles and overall improvement of facial appearance.

NCT ID: NCT05524233 Completed - Brain Fog Clinical Trials

Transcranial Direct Current Stimulation (tDCS)

tDCS
Start date: September 29, 2022
Phase: N/A
Study type: Interventional

Cognitive impairment refers to when an individual struggles to learn, concentrate, remember, or make decisions. This can be due to underlying neurological diseases (i.e. Alzheimer's disease, dementia, etc.), caused by viral illness (i.e. brain fog experienced by COVID-19 survivors) or physical trauma (i.e. concussion). Recent reports indicate that two out of three Americans experience some amount of cognitive impairment in their lifetime. There are a number of therapies that have been used to help address this condition. One of these is transcranial direct current stimulation (tDCS), which delivers sustained direct current to to the head area via electrodes. A number of studies have indicated that this form of therapy is safe and efficacious at inducing neuroplasticity and exciting neuronal activity. These factors can help improve aspects of cognitive functioning such as working memory, learning, and task performance. The purpose of this pilot study is to examine the acceptability and proof of concept effectiveness of a wireless, transcranial direct current stimulation for people with cognitive impairments.

NCT ID: NCT05524220 Completed - Clinical trials for Obstructive Sleep Apnea, Obesity

Effect of Nasal Positive Airway Pressure Versus Standard Care on Oxygenation and Ventilation During Propofol-based Sedation for Colonoscopy in Patients With High Risk of Airway Obstruction

Start date: December 19, 2022
Phase: N/A
Study type: Interventional

The purpose of this study is to to compare oxygenation and ventilation on spontaneously ventilating obese patients or those with diagnosed or undiagnosed Obstructive sleep apnea (OSA) undergoing day colonoscopy under Propofol based sedation, between the SuperNO2VA Etâ„¢ nasal positive airway pressure (PAP) device and routine care with face mask for oxygen (O2).

NCT ID: NCT05524116 Completed - Knee Osteoarthritis Clinical Trials

Telehealth Exercise and Mindfulness for Pain in Osteoarthritis

TEMPO
Start date: October 4, 2022
Phase: N/A
Study type: Interventional

This is a parallel-arm mixed-methods randomized controlled trial to investigate the feasibility of telehealth delivered mindful exercise vs. usual exercise interventions for people with knee osteoarthritis.

NCT ID: NCT05523973 Completed - Stroke, Ischemic Clinical Trials

Lingual Endurance Exercise in Treating Post-Stroke Dysphagia

Start date: August 2, 2022
Phase: N/A
Study type: Interventional

This study will enroll 15 participants in each exercise condition (groups described below). Aim 1: Determine feasibility of lingual endurance training for individuals with persistent dysphagia after ischemic stroke. Primary outcome measures: patient adherence (# of attempted repetitions/# prescribed repetitions) and dose delivery (# of repetitions meeting goal/# prescribed repetitions). Aim 2: Determine efficacy of lingual endurance training on improving critical aspects of oropharyngeal swallowing (physiologic impairments, clearance of oropharyngeal residue, airway protection), functional oral intake, and patient reported swallowing quality of life in individuals with persistent dysphagia after ischemic stroke. Primary outcome measures: improvement on videofluoroscopic assessment of swallowing function using the gold standard Modified Barium Swallowing Impairment Profile (MBSImP) Overall Impairment (OI) score and Functional Oral Intake Scale (FOIS) score. Secondary outcome measures: oropharyngeal residue - Normalized Residue Ratio Scale (NRRS); airway invasion - Penetration Aspiration Scale (PAS). Patient reported outcome measures: EAT-10 (Eating Assessment Tool) and the Swallowing Quality of Life Questionnaire (SWAL-QoL). Aim 3: Determine if lingual endurance training + transference exercise (Exercise Group #2) results in better transference of exercise effects to the aforementioned outcomes of swallow safety and efficiency (in Aim2).

NCT ID: NCT05523687 Completed - Clinical trials for Healthy Male Volunteers

AME Study of [14C]-PC14586 in Healthy Male Participants

Start date: September 6, 2022
Phase: Phase 1
Study type: Interventional

This study will assess the PK and rates of elimination and mass balance of total radioactivity from [14C]-PC14586