Lung Cancer Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- Women who are biologically female and at least 18 years old
- People who are willing to sign a written agreement to take part in the study and allow their personal data to be used
- People who own a smartphone that can run the BayPass mobile app and are willing to use it for the study
For the cancer group specifically:
- People who have been diagnosed (now or in the past) with at least one of the following cancers: breast cancer, lung cancer, colorectal cancer, or a gynecologic cancer (including ovarian, endometrial, cervical, fallopian tube, vaginal, or vulvar cancer)
Who may not be able to join:
- People with a known diagnosis of HIV, Hepatitis A, Hepatitis B, Hepatitis C, or who currently have an active COVID-19 (SARS-CoV-2) infection
- People who have a serious or potentially life-threatening illness other than the cancers listed above
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Matthias W. Beckmann, Prof. Dr. med., Head of Department of Obstetrics and Gynecology
Phone: +49 9131 85 33572
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Assessment of breast cancer risk by polygenic risk score in combination with app-based self-reported health behavior in the study population
Can't join this trial?
Data last synced from ClinicalTrials.gov: 16 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.