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Clinical Research

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Clinical Research

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Search Results 1-10 of 28 clinical trials found.

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TRACE COVID-19 (Tracking Electrocardiographic Changes in COVID-19)

In the TRACE COVID-19 study, we are investigating whether COVID-19 infection causes any changes in heart electrocardiogram (ECG) tracings that can be detected by wearable devices such as the Apple Watch. The goal is to determine whether the ECG can detect COVID-19 infection before the onset of any symptoms. Study participants will be asked to use their Apple Watch to obtain their ECG and fill out a very short survey daily. All data are de-identified (anonymized). For more details and to enroll in the study, please go to the study website: http://tracecovid19study.com

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Status: Open/Actively Recruiting
Age Group: Adult
Contact: Jeffrey Hsu
Investigator: Jeffrey Hsu

Early Detection of Health Improvement and Decline through Remote Health Monitoring in COVID-19 Positive Patients and in those with known exposure of COVID 19

The main goal of this study is to evaluate and help predict decline in at risk populations with COVID-19 or those exposed to COVID-19+ individuals who could benefit from having a remote monitoring system in their homes to provide valuable information to their care teams.

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Status: Open/Actively Recruiting
Phase: N/A
Age Group: Adult
Contact: Covid19 Clinical Research Sensing
Investigator: Arash Naeim

Immune Modulators for Treating COVID-19

ACTIV-1 IM is a master protocol designed to evaluate multiple investigational agents for the treatment of moderately or severely ill patients infected with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). The research objectives are to evaluate each agent with respect to speed of recovery, mortality, illness severity, and hospital resource utilization. Each agent will be evaluated as add-on therapy to the standard of care (SoC) in use at the local clinics, including remdesivir (provided). The SoC may change during the course of the study based on other research findings. Comparisons of the agents among themselves is not a research objective. The study population corresponds to moderately and severely ill patients infected with the coronavirus disease 2019 (COVID-19) virus. Recruitment will target patients already hospitalized for treatment of COVID-19 infection as well as patients being treated for ...

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Status: Open/Actively Recruiting
Primary Purpose: Treatment
Gender: All
Contact: Yesenia Calzada
Investigator: Otto Yang

Anti-thrombotics for Adults Hospitalized With COVID-19 (ACTIV-4)

This is a randomized, open label, adaptive platform trial to compare the effectiveness of antithrombotic strategies for prevention of adverse outcomes in COVID-19 positive inpatients

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Status: Open/Actively Recruiting
Phase: Phase IV
Primary Purpose: Treatment
Gender: All
Age Group: Adult
Contact: Julia Vargas
Investigator: George Lim

The Safety of Molnupiravir (EIDD-2801) and Its Effect on Viral Shedding of SARS-CoV-2 (END-COVID)

Designed as a multi-center, randomized, double-blind, placebo-controlled study to assess the efficacy and safety of EIDD-2801 on SARS-CoV-2 Virus Shedding in Newly Hospitalized Adults with polymerase chain reaction (PCR)-Confirmed COVID-19.

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Status: Open/Actively Recruiting
Phase: Phase II
Primary Purpose: Treatment
Gender: All
Age Group: Adult
Contact: Yesenia Calzada
Investigator: Debika Bhattacharya

ACTIV-2: A Study for Outpatients With COVID-19

Drug studies often look at the effect one or two drugs have on a medical condition, and involve one company. There is currently an urgent need for one study to efficiently test multiple drugs from more than one company, in people who have tested positive for COVID-19 but who do not currently need hospitalization. This could help prevent disease progression to more serious symptoms and complications, and spread of COVID-19 in the community. This study looks at the safety and effectiveness of different drugs in treating COVID-19 in outpatients. Participants in the study will be treated with either a study drug or with placebo.

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Status: Open/Actively Recruiting
Primary Purpose: Treatment
Gender: All
Contact: Samantha Fortier
Investigator: Kara Chew

NCI COVID-19 in Cancer Patients, NCCAPS Study

This study collects blood samples, medical information, and medical images from patients who are being treated for cancer and have a positive test for SARS CoV-2, the new coronavirus that causes the disease called COVID-19. Collecting blood samples, medical information, and medical images may help researchers determine how COVID-19 affects the outcomes of patients undergoing cancer treatment and how having cancer affects COVID-19.

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Status: Open/Actively Recruiting
Phase: N/A
Gender: All
Contact: Jenny Lester
Investigator: Beth Karlan

Covid-19 Convalescent Plasma as Prevention and Treatment for Children With Underlying Medical Conditions

This study will provide access to investigational anti-SARS-CoV-2 human convalescent plasma for pediatric patients with underlying medical conditions (cardiovascular disease, lung disease, immunosuppression) who are either infected with SARS-CoV-2 or who have had a high-risk exposure. Study participants will be transfused once with compatible convalescent plasma obtained from an individual who has recovered from documented infection with SARS-CoV-2. Safety information and pharmacokinetic data will be collected.

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Status: Open/Actively Recruiting
Phase: Phase I
Primary Purpose: Treatment
Gender: All
Age Group: Children
Contact: Michele Carter
Investigator: Jaime Deville

Study of Mavrilimumab (KPL-301) in Participants Hospitalized With Severe Corona Virus Disease 2019 (COVID-19) Pneumonia and Hyper-inflammation

Interventional, randomized, double-blind, placebo-controlled study encompassing 2 development phases (Phase 2 and Phase 3).

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Status: Open/Actively Recruiting
Phase: Phase II/III
Primary Purpose: Treatment
Gender: All
Age Group: Adult
Contact: Karla Largaespada
Investigator: Tisha Wang

Convalescent Plasma in Outpatients With COVID-19

The overarching goal of this project is to confirm or refute the role of passive immunization as a safe and efficacious therapy in preventing the progression from mild to severe/critical COVID-19 illness and to understand the immunologic kinetics of anti-SARS-CoV-2 antibodies after passive immunization.The primary objective is to determine the efficacy and safety of a single dose of convalescent plasma (CP) for preventing the progression from mild to severe COVID-19 illness. The secondary objective is to characterize the immunologic response to CP administration. This study will adults presenting to the emergency department (ED) with mild, symptomatic, laboratory-confirmed COVID-19 illness, who are at high risk for progression to severe/critical illness, but who are clinically stable for outpatient management at randomization.

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Status: Open/Actively Recruiting
Phase: Phase III
Primary Purpose: Treatment
Gender: All
Age Group: Adult
Contact: Rebecca Beutler
Investigator: Samantha Kadera

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