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NCT ID: NCT05927753 Completed - Clinical trials for Refractive Error - Myopia Bilateral

Study to Evaluate the Clinical Performance of Deseyne (Vifilcon C) Daily Disposable Soft Contact Lens

Start date: June 8, 2023
Phase: N/A
Study type: Interventional

This clinical study is to provide clinical performance data comparing the test lens (Deseyne [vifilcon C] daily disposable soft contact lens) to a control lens (1-Day Acuvue Moist [etafilcon A] daily disposable soft contact lens) in the same indication for use (single use prior to removal followed by a fresh lens upon the next lens wear exposure). The study is designed to test the hypothesis that the test lens is substantially equivalent to the control lens in like indications for use.

NCT ID: NCT05927649 Completed - Clinical trials for Health Adult Subjects

A TQTc Study for Omaveloxolone

Start date: July 11, 2023
Phase: Phase 1
Study type: Interventional

This is a randomized, double blind, placebo and active (moxifloxacin open label) controlled study in healthy subjects to assess the effect of the supratherapeutic exposure of omaveloxolone on QTc interval. Moxifloxacin will be used as an active control and will be administered as open label. Omaveloxolone and placebo will be administered in a blinded fashion. All treatments will be administered after an FDA high-fat meal. Concentration-QTc (C-QTc) analysis is the primary analysis for the study.

NCT ID: NCT05927597 Completed - Healthy Volunteers Clinical Trials

A Study of the Safety, Pharmacokinetics, and Pharmacodynamics of INS1007 in Healthy Japanese and Caucasian Participants

Start date: January 9, 2019
Phase: Phase 1
Study type: Interventional

The primary purpose of Part A of this study is to compare, in a single dose and multiple doses the safety, tolerability, and pharmacokinetics (PK) profile administered in Japanese and Caucasian participants and of Part B of the study is to assess the food effect of a single dose of INS1007 administered in Japanese and Caucasian participants.

NCT ID: NCT05927480 Completed - Clinical trials for Lower Extremity Fracture

Audio Distraction for Traction Pin Placement

ADTPP
Start date: April 25, 2018
Phase: N/A
Study type: Interventional

Traction pin placement is a common way to temporarily manage femur fractures and unstable acetabular fractures while awaiting surgery. Skeletal traction is thought to reduce patient discomfort by improving fracture alignment as well as relaxing muscle spasm pain felt from the broken bone by stretching out the leg. Skeletal traction may also help prevent articular surface damage in the hip by decreasing joint pressure. Despite the benefits of skeletal traction, insertion of the traction pin can be a painful and unpleasant experience for the patient. Our study hopes to see if listening to music with headphones during insertion of the traction pin decrease patient pain and anxiety.

NCT ID: NCT05926674 Completed - Clinical trials for N/A Healthy Individuals

Does Manual Therapy Provide Immediate Improvement in Lumbar Range of Motion?

Start date: July 15, 2023
Phase: N/A
Study type: Interventional

The goal of this clinical study is to determine if manual therapy can improve lumbar mobility in healthy individuals. The main questions it aims to answer are: - Is there an immediate local spinal effect? - Is there an associated distal effect? Researchers will compare an experimental group and a control group to examine the effects.

NCT ID: NCT05926661 Completed - Clinical trials for Heart Disease Congenital

Support Tool for Families of High-Risk Children With Heart Disease During Hospital Admission and After Discharge

Start date: November 29, 2023
Phase: N/A
Study type: Interventional

The goal of this study is to pilot the "support tool" in the Nemours Cardiac Center to assess acceptability and feasibility. This tool will be offered to 5 high-risk families, and they will be asked to complete a survey. In addition, healthcare providers including bed-side nurses and cardiologists will be asked to complete a survey to assess the feasibility of the tool.

NCT ID: NCT05926648 Completed - Healthy Clinical Trials

Form, Fit, and Function of INVSENSOR00061

Start date: May 12, 2023
Phase: N/A
Study type: Interventional

The objective of this study is to evaluate the form, fit, and function of INVSENSOR00061 when used on newborn and infant subjects 0-18 months.

NCT ID: NCT05926245 Completed - Clinical trials for Glutathione-cyclodextrin Complex Absorption

Topical Absorption of Glutathione-cyclodextrin Complex in Healthy Human Subjects Improves Immune Response Against Mycobacterium Infection

Start date: July 11, 2022
Phase: Phase 1
Study type: Interventional

The proposed clinical trial will confirm the therapeutic absorption of glutathione following topical Glutaryl application in increasing blood GSH levels without an invasive procedure. GOAL: Confirm therapeutic level of glutathione following topical transdermal application. HYPOTHESIS: The hypothesis of the proposed study is that the glutathione administration will increase RBC levels of glutathione above 80%. AIM: Determine a non-invasive way to increase glutathione levels in the plasma and blood cells. This aim will be accomplished as follows: STEP 1: We will recruit eligible healthy participants in the two study groups who are not currently taking any glutathione or N-acetyl cysteine (NAC) supplementation. STEP 2: Determine baseline levels of GSH, free radicals and cytokines through analysis of venipuncture blood draws. STEP 3: Study subjects will be asked to spray themselves with either placebo or Glutaryl four times twice a day for three days on the ventral part of the abdomen. Measure the levels of GSH, free radicals and cytokines after 1 hour, 4 hour and 72 hours.

NCT ID: NCT05926193 Completed - Hypertension Clinical Trials

Food as Medicine Project

Start date: March 30, 2023
Phase: N/A
Study type: Interventional

Causes' Fresh Produce Program (FPP) in Durham County has addressed barriers to food security related to transportation with an innovative delivery model, but lacks evidence regarding the impact of food supplementation on chronic diseases like hypertension, which is prevalent in historically excluded populations in Durham County. The goal of this research study is to determine the efficacy of the modified Dietary Approach to Stop Hypertension (DASH) diet in Black/African American and Hispanic/Latinx participants with chronic hypertension who identify as food insecure using a randomized controlled trial. This research will leverage FPP's innovative distribution system to deliver medically-tailored produce bags and provide education workshops to the experimental participants relative to their experimental group. The study population group intends to include members of the Durham community and surrounding areas that identify as members of either the Black/African American or Hispanic/Latinx populations. Success will be measured in pre- and post-intervention biomarkers and qualitative participant experience data. Recognizing the risk of using Protected Health Information of Durham community members, many of whom are members of historically excluded populations that have been subjugated to harmful and extractive research practices, steps will be taken to ensure that collected information about research participants' personal and health information is protected and used only for the purposes of research. Ultimately, this research aims to work directly with the community to address hypertension outside of the clinic using food and education delivered directly to participants. The success of such an intervention could lead to expansion of delivering medically and culturally tailored foods to the larger FPP population and beyond.

NCT ID: NCT05926050 Completed - Reaction Time Clinical Trials

The Acute Effects of a Dietary Supplement on Cognitive Performance in Highly Trained Athletes.

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

This study was designed to determine if a dietary supplement containing extracts of American ginseng, bacopa monnieri and coffee fruit can enhance cognitive performance in a population of trained athletes.