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Evaluation of depth of necrosis on histological material derived by standard bipolar TURis and by vaporisation with the Olympus PlasmaButton-electrode

Not Applicable
Conditions
N40
Hyperplasia of prostate
Registration Number
DRKS00005448
Lead Sponsor
St. Elisabeth Krankenhaus Abteilung Urologie
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Male
Target Recruitment
64
Inclusion Criteria

•patients with benign prostatic hypertrophy and indication for TURP on the basis of
- recurrent or refractory urinary retention, rest urine formation
- recurrent hematuria
- bladder stones
- recurrent urinary tract infections
•prostate volume > 30 cm3
•pre-treatment investigations completed according to currently accepted criteria for prostate surgery
- initial urologic evaluation
- indications for TURP
- pre-anaesthesia evaluation
•patients >= 18 years
•written informed consent signed by the patient

Exclusion Criteria

•local treatments of prostate or preceding prostate surgery
•Known prostate carcinoma
•palliative TURP
•preoperative long-term catheter for more than 1 week
•contraindication for lithotomy position

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
determination of necrosis depth of histological material, which is taken during two routinely operation methods
Secondary Outcome Measures
NameTimeMethod
ot applicable
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