RELIEF Study: Real-world Evaluation of LUTS Interventions and Patient Experience During Follow-up
About the study
The objective of the RELIEF Study is to compare the safety, effectiveness and patient experience outcomes in real-world subjects treated with different modalities for symptomatic BPH.
Who can take part
You may be eligible to participate in the study if you meet the following criteria:
INCLUSION CRITERIA
Inclusion Criteria:
* Diagnosis of symptomatic BPH
EXCLUSION CRITERIA
Exclusion Criteria:
- Prior surgical intervention for treatment of BPH
- Unable or unwilling to give informed consent or unwilling to complete all required questionnaires and follow-up assessments
Study Locations
Enter your ZIP code/Postal code/PIN code to locate study sites near you:
How to Apply
Contact the study center to learn if this study is a good match for you.
Study Details
Contition
Benign Prostatic Hyperplasia
Age
45+
Participants Needed
2500
Est. Completion Date
Dec 31, 2030
Treatment Type
OBSERVATIONAL
Sponsor
NeoTract, Inc.
ClinicalTrials.gov NCT Identifier
NCT05784558
Study Number
CP00022
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