Find clinical trials for COVID 19. Search for COVID 19 clinical trials in different cities and states across the United States.
COVID-19 clinical trials are research studies designed to evaluate various aspects of the disease caused by the SARS-CoV-2 virus. They typically include trials designed to understand more about the prevention, treatment, and management of COVID-19. These trials aim to develop and test new vaccines, medications, and therapeutic approaches to combat COVID-19 and mitigate its impact.
Although it might seem that COVID-19 is a disease in the past, COVID-19 clinical trials still hold high importance in the medical research landscape. As the illness continues to evolve, new variants are becoming more apparent, which means existing vaccines and treatments could become less effective. Clinical trials for COVID-19 help to develop and optimize vaccines, including evaluating the need for booster doses and new formulations. They also focus on discovering and refining treatments, addressing the long-term effects of the disease, and improving diagnostic tools.
Clinical trials for COVID-19 also ensure that interventions are tested across diverse populations, promoting global health equity and addressing disparities in healthcare access. They contribute to better preparedness for future pandemics by providing insights into rapid response strategies and effective management practices.
Several methodologies are used in COVID-19 clinical trials depending on the trial objectives and data the research team is looking to gather.
Vaccine trials are essential for developing and validating COVID-19 vaccines to ensure they are safe, effective, and capable of protecting against the virus and its variants. These trials rigorously test new vaccines through multiple clinical trial phases to assess safety, efficacy, and immune response, providing critical data needed for regulatory approval and public health use.
By evaluating how well vaccines prevent infection and reduce the severity of COVID-19, and by investigating the need for booster doses, vaccine trials contribute to achieving widespread immunity, reducing the burden on healthcare systems.
Interested in learning more about the duration and phases of vaccine clinical trials? Read all about the timelines, stages, and factors influencing the length of these trials in our guide.
Researchers use the observational method in COVID-19 clinical trials to gather real-world data on the disease's progression, treatment effectiveness, and long-term impacts. Observational studies help identify patterns and outcomes in diverse populations without intervening directly. They are particularly valuable for understanding the natural course of COVID-19, evaluating the effectiveness of treatments and vaccines in routine clinical settings, and assessing the long-term effects and complications of the disease, including "long COVID."
This approach complements interventional trials by providing insights into how interventions perform outside controlled environments and across varied demographic and health backgrounds, enriching overall knowledge and guiding public health strategies.
Researchers may use long-term impact studies in COVID-19 clinical trials to understand and address the enduring effects of the virus on health and quality of life. These studies track individuals over extended periods to assess chronic symptoms, complications, and overall health outcomes following the initial infection, including conditions like "long COVID."
By providing insights into the long-term consequences of COVID-19, such as persistent fatigue, cognitive impairments, and other lingering issues, these studies help inform ongoing treatment strategies, rehabilitation approaches, and public health policies to better manage the prolonged impacts of the disease.
Although COVID-19 is no longer as prevalent as it was during the height of the pandemic, it can still be beneficial to participate in a COVID-19 clinical trial. Both participants and the wider medical research community can experience the benefits of getting involved in a COVID-19 clinical trial.
Participating in a clinical trial for COVID-19 offers several benefits, including access to the latest treatments, vaccines, and preventive measures at the forefront of medical research. Participants may receive alternative and innovative therapies while benefiting from close monitoring and care, which enhances their health management.
Involvement in COVID-19 clinical trials contributes to advancing scientific knowledge, improving future public health strategies, and helping develop more effective solutions against evolving strains of the virus. By joining a trial, individuals play a crucial role in shaping the future of COVID-19 management.
There are also some risks and considerations for participants interested in joining a clinical trial for COVID-19. Firstly, they may experience side effects or adverse reactions from experimental treatments or vaccines, which may not be fully understood beforehand. The trial may also require frequent visits, testing, or adherence to strict protocols, which can be time-consuming and inconvenient.
Additionally, there is the potential for receiving a placebo or less effective treatment instead of the latest intervention. Participants should carefully review the informed consent documents, understand the study's procedures and potential risks, and discuss their participation with healthcare professionals to ensure it aligns with their health needs and expectations.
Eligibility for participating in a COVID-19 clinical trial typically depends on several factors such as age, health status, COVID-19 status, medical history, and any current treatments or medications. The eligibility of a clinical trial is determined to ensure participant safety and the validity of the trial’s results. Potential participants should consult with healthcare providers and review the specific criteria for each trial to determine suitability.
Like most clinical trials, your involvement in a COVID-19 clinical trial will start with a thorough screening process to determine whether you are eligible to take part. At this point, you’ll also learn about the purpose of the study, its potential risks and benefits, and its procedures, as well as provide informed consent.
During the trial, you may need to attend regular visits for monitoring, which could include tests, assessments, and follow-ups to evaluate the treatment’s effects and track any side effects. The trial will adhere to a specific protocol, and you’ll need to comply with its requirements, such as medication schedules or lifestyle restrictions. At the end of the trial, you’ll receive feedback on the results and any implications for your ongoing care.
Enrolling in a clinical trial studying cardiovascular conditions through our platform is a straightforward and user-friendly process. Here's how to get started:
Sponsor:
IMMUNOe Research Centers
Location:
Code:
NCT04705831
Conditions
Post-Viral Fatigue Syndrome
Post-Viral Disorder (Disorder)
Covid19
Eligibility Criteria
Sex: All
Age: 18 - 70+
Healthy Volunteers: Not accepted
Interventions
Ruconest
Sponsor:
Texas Cardiac Arrhythmia Research Foundation
Location:
Code:
NCT04830774
Conditions
COVID-19
Atrial Fibrillation New Onset
Eligibility Criteria
Sex: All
Age: 18+
Healthy Volunteers: Not accepted
Interventions
ILR, PMK, ICD
Sponsor:
Terry L. Wahls
Location:
Code:
NCT05057676
Conditions
Multiple Sclerosis
Clinically Isolated Syndrome
Fibromyalgia
Post Acute Sequelae of COVID-19
Cancer in Remission With Persisting Fatigue
Eligibility Criteria
Sex: All
Age: 18 - 70+
Healthy Volunteers: Not accepted
Interventions
Immediate Autoimmune Intervention Mastery Course (AIM)
Immediate Question and Answer sessions. (AIM Q and A sessions)
Delayed Autoimmune Intervention Mastery Course (delayed AIM course)
Delayed AIM Question and Answer sessions
Sponsor:
M.D. Anderson Cancer Center
Location:
Code:
NCT04565665
Conditions
COVID-19 Infection
COVID-19-Associated Acute Respiratory Distress Syndrome
Hematopoietic and Lymphoid Cell Neoplasm
Malignant Solid Neoplasm
Symptomatic COVID-19 Infection Laboratory-Confirmed
Eligibility Criteria
Sex: All
Age: 18+
Healthy Volunteers: Not accepted
Interventions
Best Practice
Mesenchymal Stem Cell