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EFFICACY EVALUATION OF TADALAFIL 20 MG ON DEMAND VS TADALAFIL 5 MG DAILY AS TREATMENT MODALITY FOR ERECTILE DYSFUNCTION FOLLOWING RADICAL RADIOTHERAPY IN PROSTATIC CANCER - ND

Conditions
Erectile dysfunction following radiotherapy for prostatic cancer
MedDRA version: 6.1Level: PTClassification code 10060862
Registration Number
EUCTR2007-002058-41-IT
Lead Sponsor
AZIENDA SANITARIA OSPEDALIERA S. GIOVANNI BATTISTA DI TORINO
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Authorised-recruitment may be ongoing or finished
Sex
Male
Target Recruitment
Not specified
Inclusion Criteria

- normal erectile function before radiotherapy (IIEF score > 25)

- Radiotherapy completed 6 months before

- erectile dysfunction lasting more than 3 months

- no previous LHRH analogues

- patients in a stable relationship
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range

Exclusion Criteria

- patients on hormone treatment

- previous radical prostatectomy

- patients taking nitrates

- patients with diabetes or other diseases potentially inducing neurogenic erectile dysfunction

patients with hypogonadism (total testosterone < 2 ng/ml)

Study & Design

Study Type
Interventional clinical trial of medicinal product
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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