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NCT ID: NCT04556838 Completed - Dry Eye Clinical Trials

Study of VVN001 Ophthalmic Solution in Dry Eye Disease

Start date: December 3, 2020
Phase: Phase 2
Study type: Interventional

This is a Phase 2a, multi-center, double-masked, randomized, vehicle-controlled, parallel-group study designed to evaluate the safety and tolerability and to explore the efficacy activity of VVN001 ophthalmic solution versus vehicle in subjects with dry eye disease.

NCT ID: NCT04556786 Completed - Chronic Disease Clinical Trials

A Pharmacist-led Transitions of Care Program

Start date: October 2, 2018
Phase: N/A
Study type: Interventional

This study was to show the value of pharmacists in providing transitions of care to and improving health outcomes of uninsured populations. It also aimed to demonstrate the feasibility of implementing a transitions of care program in an indigent care clinic with limited resources. We hypothesized that a pharmacist-led transitions of care program will reduce 30-day hospital readmission rates among the uninsured discharged from a community hospital.

NCT ID: NCT04556747 Completed - Pain Clinical Trials

FOREVR Peds VR Pilot

Start date: September 1, 2018
Phase: N/A
Study type: Interventional

To determine the feasibility and acceptability of using immersive virtual reality technologies to impact clinical outcomes (e.g., pain and anxiety) and medication utilization (e.g., narcotics) in pediatric patients with acute and chronic pain.

NCT ID: NCT04556734 Completed - Alopecia Areata Clinical Trials

Safety and Efficacy of Oral Etrasimod in Adult Participants With Moderate-to-Severe Alopecia Areata

Start date: July 29, 2020
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the safety and efficacy of etrasimod monotherapy (2 milligrams [mg] and 3 mg) in participants with moderate-to-severe alopecia areata (AA).

NCT ID: NCT04556591 Completed - Caregivers Clinical Trials

Mobile Technology and Data Analytics to Identify Real-time Predictors of Caregiver Well-Being

Start date: November 5, 2020
Phase: N/A
Study type: Interventional

The purpose of this study is to test whether personalized messages from an easy-to-use mobile app improve mood and stress among care partners and to see if care partners like using the app.

NCT ID: NCT04556552 Completed - Opioid Use Clinical Trials

Non-Invasive Vagal Nerve Stimulation in Opioid Use Disorders

nVNS in OUDs
Start date: November 13, 2020
Phase: Phase 3
Study type: Interventional

Subjects in this study will be patients with opioid use disorders (OUDs) based on DSM-5 criteria recruited from the greater Atlanta metropolitan region. Recruitment will be from treatment programs in the greater Atlanta Metropolitan Region including the DeKalb Community Service Board residential, detoxification and other treatment programs which with over 30,000 patient visits per year represents the largest treatment program in one of two urban counties in greater Atlanta. This trial involves a second phase after completing an exploratory study in 20 patients with OUDs to assess different timing parameters of nVNS effects on sympathetic measures and symptoms of craving, as well as modelling to verify and iteratively refine the methods for vagal nerve stimulation. The investigators in this trial will then apply nVNS comparing active (N=10) to sham (N=10) in OUD patients recently started on medication, looking at opioid craving, brain functional response with HR-PET, and cardiovascular and inflammatory biomarker responses to imagery-induced opioid drug craving.

NCT ID: NCT04556448 Completed - Clinical trials for Malocclusion, Angle Class II

RCT Comparing Invisalign and Traditional Orthodontic Treatment

Start date: January 1, 2013
Phase: N/A
Study type: Interventional

Comparison of orthodontic patients treated with aligners and traditional (clear braces)

NCT ID: NCT04556396 Completed - Nephrolithiasis Clinical Trials

Intraoperative Cone-beam CT for Percutaneous Nephrolithotomy

Start date: June 25, 2020
Phase: N/A
Study type: Interventional

Percutaneous nephrolithotomy (PCNL) is a first-line treatment for kidney stones >2cm. Frequently, patients require multiple procedures to address their stone burden. The decision to proceed with a second-look procedure is based on follow-up CT imaging, which is obtained postoperatively. In this study, we propose the use of a portable CT scan technology to obtain follow-up imaging while the patient is still under anesthesia for the initial procedure. The goal of this study is to determine whether this allows the surgeon to identify residual fragments and render the patient stone-free within a single anesthetic event.

NCT ID: NCT04556201 Completed - Kidney Stone Clinical Trials

The Performance of the SOLTIVE Laser System for Laser Lithotripsy in Kidney or Ureteral Stones

Start date: December 1, 2020
Phase: N/A
Study type: Interventional

The purpose of this study is to collect real-world evidence on the performance of the SOLTIVE™ Premium SuperPulsed Laser System for laser lithotripsy in ureteroscopy, percutaneous nephrolithotomy (PCNL) and mini PCNL for kidney and ureteral stones.

NCT ID: NCT04556149 Completed - Clinical trials for Corona Virus Infection

imPulse™ Una Full-spectrum, Over Clothing E-stethoscope

Start date: October 1, 2020
Phase:
Study type: Observational

This study generates robust clinical data to train ML/AI algorithms of the Sponsor's imPulse™ Una full-spectrum e-stethoscope for digital diagnostic feature synthesis of symptomatic SARS-CoV-2/COVID-19 biosignatures for rapid and accurate mass screening.