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NCT ID: NCT05877885 Not yet recruiting - Clinical trials for Major Depressive Disorder

Targeting Network Dysfunction in Apathy of Late-life Depression Using Digital Therapeutics

Start date: August 1, 2024
Phase: N/A
Study type: Interventional

The goal of this randomized controlled trial is to evaluate the potential of a customized digital cognitive training intervention to target aspects of brain function in apathy of late-life depression and reduce symptoms of apathy and related cognitive and behavioral deficits. The investigators hypothesize that 4 weeks of a customized digital cognitive training program will lead to changes in brain connectivity, apathy severity, and cognitive control performance.

NCT ID: NCT05893160 Not yet recruiting - Pain Clinical Trials

Effects of Sustained-release Oral Sodium Nitrite on Postoperative Pain and Recovery Following Total Knee Arthroplasty

Start date: August 1, 2024
Phase: Phase 1
Study type: Interventional

This study will determine whether a drug called sodium nitrite helps improve pain and post-operative recovery associated with knee replacement surgery.

NCT ID: NCT05897099 Not yet recruiting - HIV Infections Clinical Trials

Comprehensive HIV and Harm Prevention Via Telehealth

CHARIOT
Start date: August 1, 2024
Phase: N/A
Study type: Interventional

The purpose of this study is to test 2 different ways to offer medications to prevent human immunodeficiency virus (HIV), cure hepatitis C virus (HCV) (if applicable) and treat substance use disorder (if desired) in people who inject drugs.

NCT ID: NCT05900362 Not yet recruiting - Clinical trials for Congestive Heart Failure

Feasibility and Success Trial of Remote Patient Monitoring in Heart Failure

FAST-RPM-HF
Start date: August 1, 2024
Phase: N/A
Study type: Interventional

Previous research has investigated the use of remote patient monitoring in various clinical contexts, however there has not been a clinical trial examining use of the VitalCare platform for ambulatory management of heart failure. This trial will serve as a pilot study examining the feasibility of use of the VitalCare platform for ambulatory heart failure management and examine the effect of remote patient monitoring on patient engagement. To the investigators' knowledge, this will be the first study examining the effect of remote patient monitoring with the VitalCare platform on heart failure clinical outcomes, such as hospitalization for heart failure exacerbations and emergency room visits for heart failure.

NCT ID: NCT05901259 Not yet recruiting - Stroke Clinical Trials

The Exopulse Mollii Suit Study - a Database for Routine Follow-up of Clinical Outcomes

Start date: August 1, 2024
Phase:
Study type: Observational [Patient Registry]

The objective is to explore the potential short and long-term impact of the Exopulse Mollii Suit on subjects with CP, MS, stroke, SCI or other neurological disorders which may cause such types of symptoms, and to identify high responders among the sub-categories of the diagnoses. The primary endpoint will be improvement on the Berg/Pediatric Balance Scale (BBS) as a measurement of balance and risk of falls.

NCT ID: NCT05901272 Not yet recruiting - Depression Clinical Trials

Implementation of Collaborative Care for Depression in VA HIV Clinics

HITIDES-H3
Start date: August 1, 2024
Phase: N/A
Study type: Interventional

HIV Translating Initiatives for Depression into Effective Solutions (HITIDES) is a team-based service to manage depression in Veterans Living with HIV (VLWH). This service is more effective for managing depression than the care VLWH usually receive and saves resources. HITIDES is also liked by HIV care providers and VLWH. Despite this, no VA clinics currently offer this service. This study examines two approaches to engage clinics with HITIDES, the resulting effects on VLWH, and the costs of these approaches. The first approach includes recruiting an HIV care provider at the site to help connect with the service and a network of providers to support this person. The second approach uses an additional external expert to facilitate these connections. Understanding how to connect Veterans to the HITIDES service will allow VA to improve depression care for VLWH and save VA resources.

NCT ID: NCT05911828 Not yet recruiting - Falciparum Malaria Clinical Trials

A Study to Determine Safety, Tolerability, and Pharmacokinetics of Different Orally Administered Regimens of the Combination ZY19489-Ferroquine in Adult Asymptomatic Plasmodium Falciparum Carriers

Start date: August 1, 2024
Phase: Phase 1
Study type: Interventional

Malaria is caused by protozoan parasites of the genus Plasmodium and it is the most important parasitic disease in terms of mortality and morbidity. Estimates of 247 million malaria cases and 619.000 deaths worldwide were reported by WHO for the year 2021 (1). Plasmodium falciparum can lead to severe malaria and accounts for 90% of malaria deaths that mainly occur in children below the age of 5 years in Sub-Saharan Africa. A simplified treatment regimen, ideally a single-day cure (or at most 2-day dosing regimen), of uncomplicated malaria due to P. falciparum would be the magic in the antimalarial armamentarium. Improving treatment adherence is one of the key factors in reducing mortality and morbidity and also the transmission of malaria, and such a regimen would substantially increase adherence. To find a new non-artemisinin combination therapy with a shorter regimen, ideally, a single-dose cure, with low resistance potential would be the aim. The two compounds tested here are ZY19489, a triaminopyrimidine, and ferroquine (FQ), a next-generation 4-aminoquinoline. Both compounds show unique features in terms of long half-life, and activity against current drug-resistant strains. Therefore, the main goal of this clinical trial is to assess the safety of the ZY19489-FQ combination given as a 1- or 2-day dose regimen.

NCT ID: NCT05917002 Not yet recruiting - Healthy Clinical Trials

MPFC Theta Burst Stimulation as a Tool to Affect Rational Decision Making

Start date: August 1, 2024
Phase: Early Phase 1
Study type: Interventional

This is a study to investigate if a device that temporarily changes brain activity (repetitive transcranial magnetic stimulation, rTMS) might be used to change how healthy participants make decisions. This study involves 2 visits to MUSC that will each take between 2-3 hours. This study is not a treatment study, but it could help inform studies investigating treatment in the future. Participants in this study will be compensated for their time.

NCT ID: NCT05924672 Not yet recruiting - Clinical trials for Castration-Resistant Prostate Carcinoma

Efficacy of Ra-223 in PSMA PET Optimally Selected Patients

Start date: August 1, 2024
Phase: Phase 2
Study type: Interventional

This phase II trial studies how well prostate-specific membrane antigen (PSMA) positron emission tomography (PET) scans (in combination with bone scans) work in selecting patients for Ra-223 radiation therapy that have castration-resistant prostate cancer that has spread from where it first started (primary site) to the bones (bone metastasis). Ra-223 is a type of therapy that emits radiation. Radiation gives off energy which can kill tumor cells and other cells that may support the tumor cells. Ra-223 is given by infusion into the veins, where it is absorbed by the bones. PSMA PET is a type of scan used to detect prostate cancer tumors. PSMA is a radioactive tracer that binds to a specific protein that is found on prostate tumor cells. The PSMA tracer shows the areas on the PET scan where tumor cells are active. A PET scan uses a special camera to detect the energy given off from radioactive tracers (such as PSMA) to make detailed pictures of areas where the tracer accumulates in the body. The PET scan is often combined with a magnetic resonance imaging (MRI) or computed tomography (CT) scan, which helps to map the locations where PSMA has accumulated. PSMA PET scans may be able to select patients that will benefit the most from Ra-223 treatment.

NCT ID: NCT05946031 Not yet recruiting - Cigarette Smoking Clinical Trials

Testing the ETM: Examination and Comparison of Different Methods

Start date: August 1, 2024
Phase: N/A
Study type: Interventional

This study will experimentally assess the comparability of in-lab and remote procedures with hypothetical and real ETM purchase outcomes.