Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 3:20 AM
Ignite Modification Date:
2025-12-25 @ 3:20 AM
NCT ID:
NCT04561505
Eligibility Criteria:
Inclusion Criteria:
* prostate volume less than 80 ml
* high IPSS more than 19 affecting quality of life
* recurrent urinary retention with failure of medical treatment
* recurrent urinary tract infection
* affection of upper urinary tract
* refractory hematuria
* bladder stones
* bladder diverticula
Exclusion Criteria:
* patients with neurogenic bladder
* patients with previous prostate or urethral surgery
* associated urethral stricture
* prostate cancer diagnosed by TRUS biopsy
* prostate volume more than 80 ml
Healthy Volunteers:
False
Sex:
MALE
Study:
NCT04561505
Study Brief:
Protocol Section:
NCT04561505