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Impact of COVID-19 on GU Disease

Mitigating Risk of COVID-19 for Clinical Management of Genitourinary Diseases

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04761107
Enrollment
15240
Registered
2021-02-18
Start date
2021-02-18
Completion date
2026-02-28
Last updated
2025-01-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Benign Urologic Conditions, COVID-19 Infection, Genitourinary Cancer

Keywords

COVID-19 Infection, Biomarkers, Prostate cancer, BPH, Bladder cancer, Urinary tract infection, Kidney stone, Kidney cancer, Malignant disease

Brief summary

The purpose of this research study is to identify patients with GU disease with active or past COVID-19 infection. Participants will be asked to: * Complete an Online COVID-19 Questionnaire. * Disclose if the patient has or had Genitourinary cancer or benign urologic condition * Provide urine specimen for research * Provide 4 tablespoons of blood for testing blood for research. * Provide permission to access medical records, such as patient lab results, medical history, imaging reports, etc.

Detailed description

COVID-19 has a higher incidence in males compared to females and cancer patients have a higher risk of contracting COVID-19, and developing complications, and deteriorate more rapidly. COVID19 pandemic poses significant challenges in clinical decision-making, which has impacted management of GU patients. In order to mitigate the risk associated with COVID19 pandemic while also providing the best clinical care for patients a screening approach is essential. Clinicians taking care of cancer patients will be expected not only to understand impact of COVID19 but also incorporate a triage tool to decide which patients need immediate treatment. This prospective study presented in this IRB is about establishing a screening tool for GU patients with pre-existing cancer or with benign urological disease (e.g. BPH, kidney stone, bladder infection, urinary tract infections etc) and for those who are dealing with decisions for biopsy, active surveillance, surgery, radiation, hormonal and chemotherapy. The study team is expecting to enroll 15240 subjects under this study. Procedures involved in the study: 1. Consenting patients for the study. 2. Screening/Baseline REDCap survey to determine their COVID-19 symptoms. 3. Blood sample collection: This will be obtained for research studies including immune monitoring assays 4. Urine sample collection for bio-marker analysis. 5. Data collection from medical records, such as: * Clinical diagnoses, including date of confirmation of SARS-CoV-2 infection * Any pertinent medical history, including concomitant medications, and comorbidities that pre- date enrollment in the study, or that occur during enrollment in the study * Laboratory values from time of blood procurement * All imaging (X-ray, MRI, CAT, PAT, PSMA, Ultrasound, and Pathology etc.) performed from time of initial diagnosis until death, and any needed imaging that pre- date enrollment that may serve as a comparative to pre/post treatment imaging. * Collection time of samples in relation to study treatment * Demographic data * REDCap questionnaire, COVID-19 symptoms and severity of the symptoms

Interventions

None listed

Sponsors

Icahn School of Medicine at Mount Sinai
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
40 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Subjects must be men and women 40 years of age or older * Subjects at risk or with GU cancer (Prostate, Bladder, Kidney) * Subjects with benign GU disorders ( BPH, UTI, Bladder infection and kidney stone) * Subjects must have a GU disease that requires clinic visit as determined by physician or healthcare provider following a telehealth appointment * Willing and able to provide blood and urine samples * Willing and able to complete a questionnaire to determine the COVID-19 symptoms. * Willing and able to sign informed consent form

Exclusion criteria

* Men and women below 40 years of age * Subjects do not have a GU disease

Design outcomes

Primary

MeasureTime frameDescription
Proportion of patients with a new diagnosis of GUDay 1Proportion of patients with a new diagnosis of GU cancer and with active or past infection with SARS-Co-V-2

Secondary

MeasureTime frameDescription
Proportion of GU cancer patients, with active disease or in remissionDay 1Proportion of GU cancer patients, with active disease or in remission and with active or past infection with SARS-Co-V-2
Proportion of patients with the benign urologic conditionDay 1Proportion of patients with the benign urologic condition and with active or past infection with SARS-Co-V-2

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026