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NCT ID: NCT05228418 Not yet recruiting - Clinical trials for Alcohol Use Disorder

Bridging ED to Outpatient AUD Therapy With Naltrexone

Start date: March 2022
Phase: Phase 4
Study type: Interventional

Alcohol use disorder (AUD) is a treatable and common condition encountered in the emergency department, but unfortunately is rarely directly addressed in emergency departments nationwide. To our knowledge, initiation of medication assisted therapy (MAT) for AUD in the emergency department setting has not been widely adopted. Our project is novel for its scope to use a medication well-tested in the outpatient environment and bring it to the emergency department in order to more effectively link patients to outpatient alcohol use reduction therapy as part of a medication assisted therapy (MAT). The investigators are proposing a feasibility project to initiate oral naltrexone to eligible ED patients deemed to have alcohol use disorder and who are interested in cutting down their drinking. The investigators plan to connect these patients with outpatient follow-up in our own community practice center (CPC) for intramuscular (IM) Vivitrol injections under the supervision of the Einstein Toxicology Department. Through the CPC, patients can also be referred to other supporting services such as Alcoholics Anonymous for multidisciplinary care. The investigators are optimistic that this innovative warm hand off from the initial ED visit to outpatient follow-up will ultimately decrease problematic drinking, improve patient's health, and benefit the hospital. Our main objective is to establish a pathway to encourage patients who present to the emergency room with acute sequelae of alcohol use disorder to enter outpatient treatment. Our intervention will be the initiation of oral naltrexone with warm handoff to the Community Practice Center where patients will be transitioned to intramuscular (IM) Vivitrol for chronic maintenance therapy. Thus success will be measured by primarily: percentage of patients who make it to their first outpatient visit for the Vivitrol injection, percentage of patients who continue with treatment and continue to receive Vivitrol for their second injection.

NCT ID: NCT05219981 Not yet recruiting - Solid Tumor Clinical Trials

18F F-AraG-PET Imaging to Evaluate Immunological Response CKI Therapy in Solid Tumors Imaging

Start date: June 2022
Phase: Phase 2
Study type: Interventional

This is A pilot study of using [18F]F AraG PET imaging to evaluate the immunological response to checkpoint inhibitor

NCT ID: NCT05218980 Not yet recruiting - Healthy Lifestyle Clinical Trials

Health-related Benefits of Introducing Table Olives Into the Diet of Young Adults: Olives For Health

Start date: September 2024
Phase: N/A
Study type: Interventional

The purpose of this study is to assess whether introducing table olives into the diet results in health-related benefits for young adults. Several studies have shown that addition of olives as part of somebody's diet has a positive impact on cardiovascular, metabolic, and inflammatory factors. However, there have not been many studies among young, healthy adults. This study will compare levels of specific biomarkers, collected through blood draw, at the beginning of the study and after 5 weeks, to evaluate the effects of investigational daily olive consumption.

NCT ID: NCT05217498 Not yet recruiting - Clinical trials for Spinal Cord Injuries

Combining Low Oxygen Therapy and an Adenosine A2a Receptor Antagonist to Improve Functional Mobility After Spinal Cord Injury

Start date: September 1, 2024
Phase: Phase 1/Phase 2
Study type: Interventional

Breathing brief, moderate bouts of low oxygen trigger (low oxygen therapy, LOT) spinal plasticity (the ability of the nervous system to strengthen neural pathways based on new experiences), and improve walking after spinal cord injury (SCI). The greatest improvements in walking ability occur when LOT is administered prior to skill-based walking practice (WALK). However, the enduring benefits of LOT on walking recovery may be undermined by the accumulation of LOT-induced increase in extracellular adenosine. The goal of the study is to understand the extent to which istradefylline (adenosine 2a receptor antagonist) may limit the competing mechanisms of adenosine on LOT-induced walking recovery following SCI.

NCT ID: NCT05216679 Not yet recruiting - Plantar Fasciitis Clinical Trials

Novel Stretching Device Versus Night Splints

Start date: June 14, 2022
Phase: N/A
Study type: Interventional

A set of 100 patients previously diagnosed with plantar fasciitis will be given initial questionnaires about their symptoms and randomly assigned either night splints or the novel calf stretching device. The participants will use each device for 6 weeks. At the end of those 6 weeks, they will return for a follow up questionnaire. The answers in the questionnaire will be analyzed to compare the effectiveness of night splints to calf stretching.

NCT ID: NCT05214989 Not yet recruiting - Clinical trials for Cardiovascular Disease

Tailored Interventions to Increase Cardiac Rehabilitation Enrollment

Start date: January 1, 2025
Phase: N/A
Study type: Interventional

Cardiac rehabilitation, an outpatient program that includes supervised exercise and cardiovascular risk factor education, is one of the most important therapies for patients with cardiovascular disease. Unfortunately, very few Veterans with cardiovascular disease enroll in cardiac rehabilitation programs. This proposal will evaluate Veterans' individual barriers to attending cardiac rehabilitation with both surveys and interviews. Using this information, the investigators will develop a behavioral intervention to encourage Veterans to enroll in outpatient cardiac rehabilitation programs. This intervention will be individually tailored to Veterans with the information- motivation-behavioral skills model, a theory of behavior change. The investigators will test the tailored intervention with a proof-of-concept study in Veterans hospitalized with cardiovascular disease at the Veterans Affairs Tennessee Valley Healthcare System. This project is relevant to Veterans' health because increasing enrollment in cardiac rehabilitation will decrease mortality and increase quality of life in Veterans with cardiovascular disease.

NCT ID: NCT05213676 Not yet recruiting - Clinical trials for Congenital Diaphragmatic Hernia

Inhaled Nitric Oxide (iNO) for Congenital Diaphragmatic Hernia (CDH) - The "NoNO Trial" - a Multi-center, De-implementation, Stepped-wedge, Cluster-randomized Trial Within an Established Collaborative

Start date: January 1, 2025
Phase: Phase 4
Study type: Interventional

The purpose of this study is to Determine if deimplementation of iNO in the post-natal resuscitation/stabilization phase affects the composite outcome of ECLS use and/or mortality, as well as ECLS use, mortality, and/or oxygenation in CDH newborns and to establish the cost-effectiveness of deimplementing iNO as a therapy in the postnatal resuscitation/stabilization phase of CDH management, which will be assessed as the incremental health system costs (savings) per prevented ECLS use and/or death.

NCT ID: NCT05212246 Not yet recruiting - Clinical trials for Basal Cell Carcinoma

Basal Cell Carcinoma Chemoprevention Trial

B3C
Start date: January 15, 2025
Phase: Phase 3
Study type: Interventional

This is an intent-to-treat, split-plot design, multicenter randomized trial and the primary intervention is a double-blind comparison of Imiquimod (IMQ) vs. placebo cream for preventing basal cell carcinoma (BCC) of the skin on the face at one year and over 3 years after therapy. Participants will apply the IMQ or placebo cream to the face daily at bedtime for 12 weeks. This study will recruit 1630 Veterans at high risk of BCC from 17 VA medical centers.

NCT ID: NCT05210478 Not yet recruiting - Clinical trials for Corneal Transplantation

Intraoperative Optical Coherence Tomography for Ophthalmic Surgical Guidance - Cornea

iOCT-Cornea
Start date: January 2025
Phase:
Study type: Observational

Optical Coherence Tomography (OCT) image data will be evaluated for image quality and used to test post-processing algorithms to improve detection sensitivity for ophthalmic diseases.

NCT ID: NCT05205954 Not yet recruiting - Liver Cirrhosis Clinical Trials

HepHospital: A Hepatology Home Hospital Intervention for Patients With Advanced Liver Disease

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

This research study is evaluating a program that entails home-based care for people with advanced liver disease.