AnovaOS Network Powered Patient Registry

Anova Enterprises

Status: Enrolling

Conditions: Diseases of the Musculoskeletal System and Connective Tissue; External Causes of Morbidity and Mortality; Pregnancy, Childbirth and the Puerperium; Diseases of the Nervous System; Factors Influencing Health Status and Contact With Health Services; Symptoms, Signs and Abnormal Clinical and Laboratory Findings, Not Elsewhere Classified; Certain Conditions Originating in the Perinatal Period; Infectious Disease; Diseases of the Skin and Subcutaneous Tissue; Injury, Poisoning and Certain Other Consequences of External Causes; Diseases of the Digestive System; Congenital Malformations, Deformations and Chromosomal Abnormalities (Q00-Q99); Neoplasms; Mental and Behavioural Disorders; Diseases of the Blood and Blood-Forming Organs and Certain Disorders Involving the Immune Mechanism (D50-D89); Diseases of the Circulatory System; Diseases of the Genitourinary System; Endocrine, Nutritional and Metabolic Diseases (E00-E89); Diseases of the Respiratory System; Diseases of the Ear and Mastoid Process; Diseases of the Eye and Adnexa

Study type: Observational

Funder types: Industry

Identifiers

NCT05013944

ANOVA-001-NPPR

Details and patient eligibility

About

The objective of this study is the development, implementation and management of a registry of patient data that captures clinically meaningful, real-world, data on the diagnosis, nature, course of infection, treatment(s) and outcomes in patients with complex disease globally.

Full description

The AnovaOS™ Network Powered Patient Registry may be used to inform the development and conduct of clinical trials and observational studies designed to better understand, prevent, diagnose, treat, ameliorate or cure disease. The AnovaOS™ Network Powered Patient Registry may additionally be used to expedite identification and recruitment of participants for clinical trials of promising therapeutics and observational studies.

Enrollment: 100,000 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• 18 years old or older;
• Confirmed positive diagnosis of disease, condition or disorder. This will be self-reported or reported by the patient's provider, advocacy group or other patient representative;
• Laboratory or other independent means of confirmation is not required but may be confirmed in clinical trials;
• Able to understand and willing to sign the informed consent document; or whose legal representative has given consent to participate in the research per state and Federal requirements;
• Willing and able to complete the registry questions or have the instrument(s) completed by an informed proxy;
• Anticipated additional follow up with the registry once per year.

Exclusion criteria

• Subjects who do not meet the inclusion criteria for the study;
• Subjects who are unable to understand the protocol or unable to provide legally effective informed consent