N87
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: • Age older than 20 years • Presentation as part of the G-BA's assessment algorithm in the respective dysplasia consultation hour or unit. • signed informed consent
Exclusion criteria
Exclusion criteria: • Expected lack of compliance by the patient or inability of the patient to understand the purpose of the clinical trial • lack of patient consent
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The aim of this registry study is, on the one hand, to carry out further quality assurance in the interests of our patients. On the other hand, these data should also be used to achieve a reduction in overdiagnosis and, if necessary, therapy through better predictive power of the findings. Overdiagnosis can possibly be associated with great physical and emotional stress in women. This could then be avoided in the future. | — |
Secondary
| Measure | Time frame |
|---|---|
| In addition, the data collected represent an important basis for patient education. | — |
Countries
Germany
Contacts
Universitästklinikum Tübingen, Department für Frauengesundheit