Intraoperative temperature measurement during holmium laser enucleation of the prostate – a clinical, experimental trial

• Conditions: N40; Hyperplasia of prostate

• Registration Number: DRKS00017047
• Lead Sponsor: niversitätsklinikum Freiburg Department Chirurgie Klilnik für Urologie

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2019-04-05
• Study Completion: 2021-02-01
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: Male
• Target Recruitment: 15

Inclusion Criteria

All male patients (>18yrs) treated with a holmium-laser-enucleation of the prostate in the clinic of urology, department surgery, University medical center, Freiburg im Breisgau.

Exclusion Criteria

children <18yrs and female

Study & Design

• Study Type: observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
temperature increase - meausrements during the whole surgery. Frequency of measurements at least 1 Hz

Secondary Outcome Measures

Name	Time	Method
Surgical outcome: <br>Voiding, residual urine, ICIQ (International Consultation on Incontinence Questionnaire), IIEF (International Index of Erectile Function), IPSS (International Prostate Symptom Score)<br><br>time of outcome meaurements: postoperatively, 3 months, 6 months