Showing page 3 of 8 - total 77 results found.
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A Randomized Trial to Evaluate Sequential vs Simultaneous Patching
https://clinicaltrials.llu.edu/trials/randomized-trial-evaluate-sequential-...A randomized trial to determine whether simultaneous treatment with spectacles and patching has an equivalent VA outcome compared with sequential treatment, first with spectacles alone followed by patching (if needed), for previously untreated amblyopia … -
Extension Study to Evaluate the Long-Term Outcomes of Pediatric Patients Who Received Treatment for Retinopathy of Prematurity in the VGFTe-ROP-1920 Study (Acronym: Butterfleye Next)
https://clinicaltrials.llu.edu/trials/extension-study-evaluate-long-term-ou...Primary objectives of the study are: * To evaluate binocular visual acuity at the end of this study in patients included from the VGFTe-ROP-1920 study, for treatment of Retinopathy of Prematurity (ROP). * To evaluate long-term safety outcomes in patients … -
Melatonin Adolescent Research Study
https://clinicaltrials.llu.edu/trials/melatonin-adolescent-research-studyThe present study will use a within-person, randomized cross-over experimental design to test the effects of exogenous melatonin supplementation on the sleep and daytime functioning of typically developing adolescents with short or disrupted sleep of … -
PROACTIVE-HF IDE Trial Heart Failure NYHA Class III
https://clinicaltrials.llu.edu/trials/proactive-hf-ide-trial-heart-failure-...This is a prospective, open- label, single arm, multicenter clinical trial to evaluate the safety and effectiveness of the Cordella PA Sensor System in NYHA Class III Heart Failure Patients compared to a Performance Goal (PG). Conditions Heart Failure … -
A Comparison of Conventional Physical Therapy, Powered Exoskeleton, and Hybrid Physical Therapy With Exoskeleton
https://clinicaltrials.llu.edu/trials/comparison-conventional-physical-ther...The purpose of this investigator-initiated study is to establish if powered exoskeleton therapy as a part of a rehabilitation program can be used as a standard of care in stroke rehabilitation. Conditions Stroke Intervention Hybrid combination of physical … -
Fenofibrate for Prevention of DR Worsening
https://clinicaltrials.llu.edu/trials/fenofibrate-prevention-dr-worseningThis randomized trial will evaluate the effect of fenofibrate compared with placebo for prevention of diabetic retinopathy (DR) worsening through 6 years of follow-up in eyes with mild to moderately severe non-proliferative DR (NPDR) and no CI-DME at … -
Bridge to HOPE: Hypothermic Oxygenated Perfusion Versus Cold Storage Prior to Liver Transplantation
https://clinicaltrials.llu.edu/trials/bridge-hope-hypothermic-oxygenated-pe...This is a prospective, multi-center, controlled, randomized, pivotal study to evaluate the safety and effectiveness of the VitaSmart Liver Machine Perfusion System by comparing clinical outcomes in patients undergoing liver transplantation with ex-vivo … -
Effect of Magnesium Sulfate Bolus on Intraoperative Neuromonitoring
https://clinicaltrials.llu.edu/trials/effect-magnesium-sulfate-bolus-intrao...Magnesium Sulfate(MgSo4) is increasingly being used as part of the multimodal pain regimen in the perioperative period. The intraoperative neurophysiological monitoring (IONM) is utilized in complex spine and cranial surgeries to assess the functional … -
Study of Lenacapavir for HIV Pre-Exposure Prophylaxis in People Who Are at Risk for HIV Infection
https://clinicaltrials.llu.edu/trials/study-lenacapavir-hiv-pre-exposure-pr...The goal of this clinical study is to test how well the study drug, lenacapavir (LEN), works in preventing the risk of HIV. Conditions Pre-Exposure Prophylaxis of HIV Infection Intervention Oral Lenacapavir (LEN) F/TDF Sub-cutaneous (SC) Lenacapavir (LEN) … -
Pivotal-Safety and Therapeutic Measures of tDCS in Patients With Refractory Focal Epilepsy
https://clinicaltrials.llu.edu/trials/pivotal-safety-and-therapeutic-measur...This is a multiple site, randomized, double blinded parallel-group controlled study. The purpose of this study is to evaluate efficacy, safety, and tolerability of repeated, daily sessions with the STARSTIM device, which delivers transcranial cathodal …