Comparison of Holmium Laser Enucleation of the Prostate (HoLEP) versus MOSESTM Laser Enucleation of the Prostate (MoLEP) in Benign Prostate Syndrome (BPS) - a prospective randomized non-inferiority study

Not Applicable

• Conditions: N40; Hyperplasia of prostate

• Registration Number: DRKS00030642
• Lead Sponsor: niversitätsklinikum Frankfurt Klinik für Urologie

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2023-01-03
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Pending
• Sex: Male
• Target Recruitment: 152

Inclusion Criteria

Indication for subvesical deobstruction

Exclusion Criteria

Prostate less than or equal to 30ccm, urethral stricture, punch biopsy confirmed carcinoma of the prostate, preoperative evidence of prostate carcinoma, neurogenic bladder emptying disorder

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
postoperative difference in micturition symptoms, which will be collected using the International Prostate Symptom Score (IPSS) questionnaire at inclusion in the study and 3, 6 and 12 months postoperatively

Secondary Outcome Measures

Name	Time	Method
Complications, uroflow (Qmax), residual urine, operating times, catheter time, hospital length of stay and sexual/ejaculatory function