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NCT ID: NCT04973254 Completed - HIV Infections Clinical Trials

Improving Treatment and Retention Adherence in Nontraditional Settings

I-TRAINS
Start date: February 23, 2022
Phase: N/A
Study type: Interventional

This is a hybrid implementation-effectiveness study using both qualitative and quantitative methods. The research aims to examine whether providing a new, but approved, HIV once a month injection treatment [Cabotegravir-Rilpivirine Long Acting (CAB-RPV LA)] to individuals who are living with HIV outside of the standard doctors office or clinic increases adherence to treatment. This HIV monthly injections treatment which is already being delivered within the clinic setting, will be administered to participants in community partner spaces, reducing the barriers that having to present to a traditional clinic for treatment creates. Individuals who will receive the injection need to have a history of being unable to take their HIV oral medication, as well as other barriers to care that make it difficult to engage in a traditional clinic setting. These barriers may include, but are not limited to, homelessness, substance use, mental illness, and stigma around their diagnosis. Data will be collected on whether it was easier for the participants to receive care in a non-traditional setting, as well as whether the injection made it easier for them to remain adherent to their HIV medication in comparison to standard oral HIV medication.

NCT ID: NCT04973228 Completed - Clinical trials for Seborrheic Dermatitis

Trial of PDE4 Inhibition With Roflumilast (ARQ-154) Foam 0.3% for the Management of Seborrheic Dermatitis (STRATUM)

Start date: July 8, 2021
Phase: Phase 3
Study type: Interventional

This phase 3, double-blind, vehicle-controlled study assessed the safety and efficacy of roflumilast (ARQ-154) foam 0.3% applied once daily (qd) for 8 weeks by participants with seborrheic dermatitis.

NCT ID: NCT04973111 Completed - Diabetes Clinical Trials

A Study to Assess CT-868 and the Relationship Between Insulin Secretory Response and Ambient Blood Glucose.

Start date: July 12, 2021
Phase: Phase 1
Study type: Interventional

A Study to Assess the Effect of CT-868 and the Relationship Between Insulin Secretory Response and Ambient Blood Glucose in Obese Male Subjects and Subjects with T2DM.

NCT ID: NCT04973085 Completed - Healthy Clinical Trials

Neck Cooling as a Non-Invasive Method to Lower Brain Temperature in Healthy Adults

Start date: July 22, 2021
Phase: N/A
Study type: Interventional

The objective of this study was to clarify whether neck cooling can be used to non-invasively lower brain temperature in healthy adults.

NCT ID: NCT04972916 Completed - Tobacco Use Clinical Trials

Patient Navigation-based Tobacco Harm Reduction Program Among Cancer Patients

Start date: June 15, 2021
Phase: N/A
Study type: Interventional

The purpose of this study is to examine the feasibility and preliminary efficacy of patient navigation to promote linkage to smoking cessation treatments in cancer patients.

NCT ID: NCT04972227 Completed - Schizophrenia Clinical Trials

Study to Assess the Safety and Pharmacokinetics of CY6463 in Participants With Stable Schizophrenia

Start date: September 10, 2021
Phase: Phase 1
Study type: Interventional

The primary objective of this study is to evaluate the safety and tolerability of CY6463 when administered to participants with stable schizophrenia who are on a stable antipsychotic medication regimen

NCT ID: NCT04972123 Completed - Syncope, Vasovagal Clinical Trials

The Effect of CPC on Aborting Tilt Induced Syncope in Patients With a History of Vasovagal Syncope or Near Syncope

Start date: July 20, 2021
Phase: Phase 2
Study type: Interventional

Syncope is defined as transient loss of consciousness associated with inability to maintain postural tone with rapid and spontaneous recovery. The purpose of this study is to assess the effects of sublingual administration of a new medication called CPC on tilt-induced syncope in patients with a history of vasovagal syncope (VVS) or near syncope. 140 participants were randomized at the University of Wisconsin - Madison. Each participant will be in the study for 1 day.

NCT ID: NCT04971928 Completed - Hepatitis B Clinical Trials

Phase 1 Study of GSK3228836 Pharmacokinetics in Participants With Hepatic Impairment

Start date: September 7, 2021
Phase: Phase 1
Study type: Interventional

This is a Phase 1, open-label, parallel-group study to evaluate the pharmacokinetics of GSK3228836 in participants with Child-Pugh B (CP-B) cirrhosis (moderate hepatic impairment), Child-Pugh A (CP-A) cirrhosis (mild hepatic impairment) and participants with normal hepatic function as healthy control.

NCT ID: NCT04971837 Completed - Pharmacokinetics Clinical Trials

Interaction Between Cannabidiol, Meal Ingestion, and Liver Function

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

According to a recent consumer poll, over 20 million Americans regularly use cannabidiol (CBD). Moreover, 64 million Americans (over 25% of the population) report trying CBD at least once within the previous 2 years. Since the passing of the 2018 Agriculture Improvement Act, the use of hemp-derived products, such as CBD, is highly prevalent across North America. The acceleration of the use of CBD has outpaced our understanding of the associated potential risks and benefits, and the way it is processed within the body. In the current proposed project, investigators wish to continue our ongoing collaboration with Caliper Foods, a Colorado-based manufacturer of CBD products. The focus of this project is three-fold: (1) investigators will compare the pharmacokinetics of different formulations of ingestible CBD; (2) investigators will examine the potential two-way interaction between a meal and one formulation of ingestible CBD; and, (3) investigators will examine the influence of different formulations of CBD on markers of liver function.

NCT ID: NCT04971811 Completed - Eating Behavior Clinical Trials

Effects of Energy Density on Self-served Snacks in Preschool Children

Start date: September 15, 2021
Phase: N/A
Study type: Interventional

The purpose of the study is to determine whether the energy density of snack foods affects the amounts that preschool children serve themselves and then consume. We will serve snacks that vary in energy density to preschool children in their childcare centers and measure the amount they serve themselves and consume. The results will have implications for guidance about the provision of snacks for preschool children and may help in identifying strategies for the prevention of obesity in children.