Database for the Assessment of Efficacy and Safety of BPH Treatment
Recruiting
Observational Study
Lower Urinary Tract Symptoms
Benign Prostatic Hyperplasia
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
At a Glance
- Age
- 18 and older
- Sex
- Male
- Study type
- Observational
- Participants needed
- 500 (estimated)
- Sponsor
- Dominik Abt · Other
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About This Trial
This registry study aims to collect data on efficacy and safety of different treatments of benign prostatic enlargement (BPE) and lower urinary tract symptoms associated with benign prostatic hyperplasia (BPH-LUTS).
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* All patients treated for BPH / LUTS / prostatic obstruction at the urological department of KSSG
* Patient age ≥ 18 years
* Informed consent provided
Exclusion Criteria:
-Cognitive impairment not allowing Informed Consent or adequate data assessment.
Contacts