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NCT ID: NCT04841525 Completed - Clinical trials for Autism Spectrum Disorder

Autism Biomarker Consortium for Clinical Trials (ABC-CT): Follow-up Study

ABC-CT
Start date: April 9, 2021
Phase:
Study type: Observational

This is a multicenter longitudinal follow-up study to the main study of an a registered already (NCT# ). The Follow-up Study (T4) will assess the Main Study cohort for an additional longitudinal time point approximately 2-5 years after the initial study. Children participating in the Follow-up Study will be approximately 8-16 years old. The aims of the main study is to identify, develop and validate a set of measures that can be used as stratification biomarkers and/or sensitive and reliable objective measures of social impairment in autism spectrum disorders (ASD) that could serve as markers of long term clinical outcome.

NCT ID: NCT04841499 Completed - Menopause Clinical Trials

Effects of a Seven-day BASIS™ Supplementation on Menopausal Syndromes and Measurements of the Urinary Vitamin B3 and Estradiol Levels in Pre-, Peri- and Post-menopause

Start date: April 5, 2021
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether a short supplementation (7days) with BASIS™ increases the natural production of estradiol, measured in urinary waste. The overall objective is to determine whether through increased estradiol levels, the undesirable menopausal effects, assessed via questionnaires, are mitigated by a short-term supplementation with BASIS™

NCT ID: NCT04841473 Completed - Concussion, Brain Clinical Trials

The TRAIN Study: A Concussion Prevention Strategy in Middle Schools

Start date: May 17, 2021
Phase: N/A
Study type: Interventional

Purpose: The purpose of this study is to evaluate the effectiveness of a theory-driven intervention (TRAIN concussion education) to improve parental concussion-related attitudes, beliefs, intentions, confidence in knowledge, and self-efficacy. Participants: 180 parents of United States middle school aged children whose children have been engaged in organized sports within the past 2 years. Procedures: The study is a single-blind (participants) randomized control trial. The investigators will randomize eligible parents into two groups: (1) control (standard concussion education); and treatment (standard concussion education AND TRAIN concussion education) to evaluate the effectiveness of the TRAIN concussion education intervention.

NCT ID: NCT04841460 Completed - Cholesterol, LDL Clinical Trials

Impact of Beef's Unique Food Matrix on Human Health

Start date: February 18, 2019
Phase: N/A
Study type: Interventional

The primary goal of the proposed research is to document changes in plasma lipoprotein fractions, including high-density lipoprotein (HDL) and low-density lipoprotein (LDL) particle sizes and functionality, following the ground beef interventions. This specifically addresses the hypothesis that increasing the amount of fat in ground beef reduces risk factors for cardiovascular disease. Also, the investigators will measure changes in glucose, insulin, and triacylglycerols (TAG) following low-fat and high-fat ground beef interventions. An important aspect of this research is that the investigators will confirm that consumption of high-fat ground beef will reduce carbohydrate intake and increase insulin sensitivity in men. Furthermore, the investigators will be able to establish which protein sources are voluntarily replaced by the low- and high-fat ground beefs.

NCT ID: NCT04841356 Completed - Clinical trials for Total Knee Arthroplasty

Swelling Management After Total Knee Arthroplasty

Start date: April 1, 2021
Phase: N/A
Study type: Interventional

The purpose of this feasibility study is to estimate the initial efficacy and feasibility of an inelastic compression garment donned immediately after TKA on peak swelling in 14 subjects.

NCT ID: NCT04841343 Completed - Sinusitis Clinical Trials

Triamcinolone Packing Following Endoscopic Sinus Surgery

Start date: January 29, 2021
Phase:
Study type: Observational [Patient Registry]

Endoscopic sinus surgery (ESS) is a well-established treatment strategy for medically refractory chronic rhinosinusitis. Middle meatus spacers are currently used following ESS to prevent scarring, synechiae formation, and middle turbinate lateralization. A 2012 systematic review favored spacers compared to no spacers, with a follow up 2013 systematic review finding no difference between the use of absorbable and non-absorbable spacers. This review, however, noted that steroidal spacers may reduce middle meatus scarring and adhesions. More recent data has shown the effectiveness of steroid releasing middle meatus implants in preventing middle turbinate lateralization, reducing synechiae formation, and reducing revision surgery. However, these stents are costly, and may result in excess crusting postoperatively, which limits their use in some settings. Another study investigated the use of steroid-impregnated absorbable packing materials, and demonstrated the safety and utility of this method of middle meatus packing. However, a limitation to this study was overall low enrollment with only 19 total patients enrolled. The purpose of this project is to add to the existing body of evidence regarding middle meatus spacers, by studying the impact of steroid impregnated, bioabsorbable hemostatic packing (Hemopore®, Stryker) on postoperative visualization and scar formation.

NCT ID: NCT04841330 Completed - Clinical trials for Peripheral Intavenous Catheter Stabilization

Prospective Healthy Volunteer Study of the Securis™ Stabilization Device

Start date: June 9, 2021
Phase:
Study type: Observational

This study is being conducted to assess the performance of the Securis™ Stabilization Device in simulated clinical use.

NCT ID: NCT04841317 Completed - Hypertension Clinical Trials

Mobile Technology for Blood Pressure Management

Start date: March 31, 2021
Phase: N/A
Study type: Interventional

The primary objective of this study is to assess the feasibility and effectiveness of a mobile-technology based system that integrates patient-facing and clinician-facing components to assist the management of hypertension.

NCT ID: NCT04841083 Completed - Migraine Clinical Trials

Narrow Band Green Light and Migraine

Start date: December 15, 2020
Phase: N/A
Study type: Interventional

Study volunteers are asked to use the Allay Lamp routinely during the 6-week study period. A web based survey is provided when the Lamp is purchased for study volunteers to complete. A daily usage paper diary is sent with the lamp so that volunteers can keep track of the frequency and duration of lamp usage and any noticeable benefits. At the end of six weeks a second survey is sent to study volunteers to capture their perceptions of potential lamp benefits with respect to headache frequency and their experience of migraine specific symptoms.

NCT ID: NCT04840914 Completed - Clinical trials for Chronic Heart Failure With Reduced Ejection Fraction

A Study of LY3461767 in Participants With Chronic Heart Failure With Reduced Ejection Fraction

Start date: June 1, 2021
Phase: Phase 1
Study type: Interventional

The main purpose of this study is to determine the tolerability and safety of LY3461767 with any side effects that might be associated with it. Study drug will be provided in a continuous subcutaneous infusion lasting 24 hours to 96 hours, depending on the cohort. Blood tests will be performed to check concentrations of LY3461767 in the bloodstream and how long it takes the body to get rid of it in participants with chronic heart failure with reduced ejection fraction (HFrEF). The study will last up to 3 months and may include 5 visits.