The evaluation of the adverse effects in the prostate cancer patient who received a focal brachytherapy.
Not Applicable
Recruiting
- Conditions
- Prostate caner
- Registration Number
- JPRN-UMIN000026453
- Lead Sponsor
- Tokyo Metropolitan Police Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Male
- Target Recruitment
- 20
Inclusion Criteria
Not provided
Exclusion Criteria
Patients must not be under these conditions 1) Patients who had past surgical histories of benign prostatic hyperplasia. 2) Patients who had severe mental disorders. 3) Patients who had other active cancers 4) Patients who doctors judge as unsuitable for this study
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method recovery periods from urinary dysfunctions after treatments it is assessed after the treatments by using IPSS, OABSS, IIEF5, FACT-P, NIHCPSI 1 month, 3 months and every 3 months afterwards.
- Secondary Outcome Measures
Name Time Method sexual function assessed by using IIEF5 rectal bleeding