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NCT ID: NCT05163782 Completed - Foot Drop Clinical Trials

Validation of an Ankle Foot Orthosis With Anterior Support for Foot Drop

Start date: July 19, 2021
Phase: N/A
Study type: Interventional

The objective of this research is to compare the new ankle foot orthosis (AFO) with prior support developed by Turbomed, with the AFO with posterior support from Turbomed as well as two competing AFOs currently on the market. With this research, we seek to answer the following questions: - Is the new AFO as biomechanically efficient as the AFOs currently on the market? - Is the new AFO more comfortable than the AFO currently on the market? - Is the new AFO easier to put on and attach than the AFOs currently on the market?

NCT ID: NCT05163431 Completed - Hallux Valgus Clinical Trials

Dimensional Validation of the Hallux Valgus Orthosis

Start date: July 20, 2021
Phase: N/A
Study type: Interventional

The goal of this project is to optimize the design of the orthosis by establishing the key volumetric characteristics of the custom iterations in order to subsequently transpose them to a standard model and establish the increment proportions of the different sizes. The final product should reduce the pain by repositioning the phalanges of the first toe with the first metatarsal in its axis.

NCT ID: NCT05161832 Completed - Kinesiophobia Clinical Trials

Impact of Kinesiophobia on Descending Corticospinal and Bulbospinal Projections

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

Fear of movement (kinesiophobia) is a phenomenon commonly observed in people suffering from chronic pain. The aims of this project are to better understand the neurophysiological basis of this phenomenon, in particular 1) the effect of kinesiophobia (induced by nocebo intervention) on the excitability of corticospinal projections and 2) the association between kinesiophobia and top-down inhibitory mechanisms.

NCT ID: NCT05160090 Completed - Bioequivalence Clinical Trials

Single Dose Crossover Comparative Bioavailability Study of Bupropion Hcl MR Tablet 300mg

Start date: January 18, 2020
Phase: Phase 1
Study type: Interventional

The objective of this study is to determine the bioequivalence of 2 different formulations of bupropion after a single oral dose administration under fasting conditions. The secondary objective of this study is to evaluate the safety and tolerability of the Test and Reference formulations in healthy subjects.

NCT ID: NCT05158023 Completed - Atopic Dermatitis Clinical Trials

Phase 2b Study of ASLAN004 in Adults With Moderate-to-Severe Atopic Dermatitis

Start date: March 16, 2022
Phase: Phase 2
Study type: Interventional

Phase 2b study designed to evaluate the efficacy and safety of ASLAN004 in adult patients with moderate-to-severe Atopic Dermatitis (AD) who are candidates for systemic therapy. This study will have 5 treatment arms (4 active and 1 placebo).

NCT ID: NCT05155748 Completed - Dementia Clinical Trials

Deprescribing Intervention Among Nursing Home Residents With Major Neurocognitive Disorders

OptimaMedLTC
Start date: December 6, 2016
Phase: N/A
Study type: Interventional

Canadians with neurocognitive disorders often are admitted to nursing homes when their disease reaches an advanced stage. At the end of their life, they may encounter adverse symptoms related to medications they no longer need, while they should receive comfort care. This study proposes an intervention to reduce the use of inappropriate medications among residents of nursing homes with major neurocognitive disorders. For that purpose, nursing homes' nursing staff, physicians and pharmacists will receive education and tools for the review, adjustment or discontinuation of the medications that have become inappropriate for the residents. The residents' families will receive information regarding the complexity of drug treatment for elderly patients with major neurocognitive disorders and they will be kept informed about the proposed changes to their relative's medication. The intervention is expected to reduce the medication load while improving or maintaining the residents' well-being.

NCT ID: NCT05155410 Completed - Clinical trials for Diabetes Mellitus, Type 2

Examining the Effect of Exogenous Ketone Supplementation on Glucose Control in Type 2 Diabetes

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

Ketone bodies are a fuel source and signaling molecule that are produced by the body during prolonged fasting or if an individuals consistently eats a low-carbohydrate "keto" diet. Blood ketones can be used as a source of energy by the body, but they may also act as signals that impact the functioning of different cells in the body. Recently, the availability of ketone supplements that can be taken orally allows for raising blood ketones without having to fast or eat a "keto" diet. The investigators' studies and those of other researchers have shown that ketone supplementation can lower blood sugar without having to make any other dietary changes. Oral ingestion of ketones may therefore be an effective strategy to improve blood sugar control and influence how cells function. The main objective of this study is to determine if consuming a ketone supplement 3 times per day (before meals) for 14 days lowers blood sugar and impacts how the body's cells function. The results of this study will be used to guide future recommendations on the utility of ketone supplements for improving health in individuals with, or at elevated risk of, type 2 diabetes.

NCT ID: NCT05154968 Completed - Clinical trials for Healthy Participants

A Study of Two Formulations (Both Refrigerated and Room Temperature) Using an Autoinjector Device in Healthy Participants

Start date: November 24, 2021
Phase: Phase 1
Study type: Interventional

The main purpose of the study is to assess the injection site pain intensity of two formulations using prefilled autoinjector device in healthy participants.

NCT ID: NCT05154864 Completed - Inflammation Clinical Trials

Ultrafiltration in Pediatric Cardiac Surgery: An Observational Cohort Study

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

Infants and children undergoing cardiac surgery with cardiopulmonary bypass (CPB) can experience systemic inflammation that prolongs post-operative recovery. Ultrafiltration is an intra-opreative technique that is hypothesized to extract circulating inflammatory mediators during the CPB time. There have been only a few small studies looking at a limited number of inflammatory marker profiles in this context. Our institution uses an innovative form of ultrafiltration "subzero-balance simple-modified ultrafiltration" (SBUF-SMUF) throughout the entire CPB time. SBUF-SMUF has been our standard of care for the last 5 years. This observational seeks to describe the clinical and immunologic outcomes of infants and children undergoing cardiac surgery with CBP and SBUF-SMUF.

NCT ID: NCT05154123 Completed - Clinical trials for Healthy Volunteer Study

Drug-drug Interaction Study of Rosuvastatin and AT-527 (R07496998)

Start date: November 16, 2021
Phase: Phase 1
Study type: Interventional

Drug-drug interaction study of rosuvastatin and AT-527 (R07496998)