Actively Recruiting
AnovaOS Network Powered Patient Registry
Led by Anova Enterprises, Inc · Updated on 2024-01-30
100000
Participants Needed
1
Research Sites
52 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are developing and managing the AnovaOS Network Powered Patient Registry to collect real-world patient data across various diseases globally. This registry aims to capture meaningful clinical information on diagnosis, infection course, treatments, and outcomes to enhance understanding and support future clinical trials and observational studies. The registry serves as a resource to better understand, prevent, diagnose, and treat diverse health conditions. Participants' data will be gathered through this registry, which can also be used to recruit individuals for clinical trials and observational studies on promising therapies. The registry collects ongoing information on patients' health status and treatments, enabling long-term monitoring and analysis. This observational study does not involve administering treatments but focuses on data collection and management. Participants will provide information through questionnaires or instruments, either personally or via an informed proxy, with an expected follow-up once per year. The research team will assess natural history, clinical effectiveness, safety, and quality of care over a period of five years. The registry includes patients with a wide range of conditions, and participation requires informed consent and the ability to complete follow-up data collection.
CONDITIONS
Brief Title
AnovaOS Network Powered Patient Registry
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 18 years old or older
- Confirmed positive diagnosis of disease, condition or disorder (self-reported or reported by a provider or representative)
- Able to understand and willing to sign the informed consent document or have a legal representative provide consent
- Willing and able to complete the registry questions or have them completed by an informed proxy
- Anticipated additional follow-up with the registry once per year
You will not qualify if you...
- Subjects who do not meet the inclusion criteria
- Subjects who are unable to understand the protocol or provide legally effective informed consent
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 5 years
Participants complete registry questions and are followed to better understand and assess disease progression, treatment effectiveness, safety, and quality of care over time.
Annual follow-up visits or assessments
Trial Site Locations
Total: 1 location
1
Anova Enterprises, Inc.
Arlington Heights, Illinois, United States, 60005
Actively Recruiting
Research Team
C
Christopher Beardmore
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
Similar Trials
Frequently Asked Questions
Have more questions? Get in touch with our team for quick support
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here