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临床试验/RBR-9y5fbs
RBR-9y5fbs尚未招募1 期

se of the penile clamp and quality of life in Urinary Incontinence After Prostatectomy: clinical trial Phase I / II

Faculdade de Enfermagem da Universidade Estadual de Campinas0 个研究点开始时间: 2016年11月1日最近更新:
适应症

试验速览

阶段
1 期
状态
尚未招募
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18Y 至 100Y(—)
性别
Male

入选标准

  • have stress urinary incontinence; have completed prostatectomy or transurethral resection for at least one year; have satisfactory score on the Mini Mental State Examination; have normal sensation in the perineum and the penis by physical examination; perineal intact skin; good manual dexterity demonstrated with installing and removing the clamp; to read and write or come with caregiver or family member, in the case of illiterate patients.

排除标准

  • be performing radiotherapy or chemotherapy for prostate tumor; have symptoms of urge urinary incontinence or urge incontinence; prior urodynamic study demonstrating detrusor overactivity or low compliance; present neurological disorders or other conditions that alter the perineal sensitivity, manual dexterity or change in cognitive function; provide blood flow velocity in lower systolic peak 10ml per seconds in the flaccid penis; be in use of penile prosthesis; be in the presence of urinary tract infection, but after resolution of the urinary tract infection, may be part of the survey, provided it meets the other eligibility criteria.

研究者

发起方
Faculdade de Enfermagem da Universidade Estadual de Campinas

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