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Search / Trial NCT06962670

Predicting Cancer Risk With Digital and Molecular Markers

Launched by UNIVERSITY OF ERLANGEN-NÜRNBERG MEDICAL SCHOOL · Apr 29, 2025

Trial Information

Current as of June 26, 2025

Recruiting

Keywords

ClinConnect Summary

This clinical trial is focused on finding new ways to predict the risk of developing certain types of cancer, particularly breast cancer. Researchers will look at information from both cancer patients and healthy individuals to identify differences that may indicate a higher risk for developing cancer. These differences could include specific biological markers, lifestyle choices, or family health history.

To participate in this study, women aged 18 and older who have a smartphone capable of running a specific app called BayPass are eligible. Participants must also be willing to consent to the study and share their personal data. Those currently diagnosed with breast, lung, colorectal, or gynecologic cancers can join as part of the case group. During the trial, participants can expect to contribute information that may help researchers better understand cancer risks, ultimately aiming to improve early detection and prevention strategies. It's important to note that individuals with certain health conditions, such as HIV or severe illnesses, are not eligible to participate.

Gender

FEMALE

Eligibility criteria

  • Inclusion Criteria:
  • 1. Biological adult (at least 18 years old) women
  • 2. Written informed consent for study participation and processing of personal data
  • 3. Own smartphone that can run the BayPass mobile application and willingness to use said smartphone for study purposes
  • Additional inclusion criterion for case group:
  • 4. Pre-existing or current diagnosis of at least one of the following oncological diseases: breast cancer, lung cancer, colorectal cancer, gynecologic cancer (incl. ovarian cancer, endometrial cancer, cervical cancer, fallopian tube cancer, vaginal cancer and vulvar cancer)
  • Exclusion Criteria:
  • 1. Known infection with HIV (Human Immunodeficiency Virus), HepA (Hepatitis A), HepB (Hepatitis B), HepC (Hepatitis C) or active SARS-CoV2 (Severe acute respiratory syndrome coronavirus type 2) infection
  • 2. Acute severe or potentially life-threatening illness, except those specified in inclusion criterion #4

About University Of Erlangen Nürnberg Medical School

The University of Erlangen-Nürnberg Medical School is a prestigious institution dedicated to advancing medical research and improving healthcare outcomes through innovative clinical trials. Renowned for its interdisciplinary approach, the medical school fosters collaboration among experts in various fields, enabling the development of cutting-edge therapies and treatment protocols. With a commitment to ethical standards and patient safety, the institution actively contributes to the global medical community by conducting rigorous clinical studies aimed at enhancing the understanding and management of diverse health conditions.

Locations

Please Refer To Project Homepage For Details (See Link Below), Bavaria, Germany

Patients applied

0 patients applied

Trial Officials

Matthias W. Beckmann, Prof. Dr. med.

Study Director

Head of Department of Obstetrics and Gynecology

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported