Colipral® (Probiotic Strain Escherichia Coli 5C (ECP24®)) for Prevention of Recurrent Cystitis in Menopausal Women
Study to Evaluate the Efficacy and Safety of Colipral® (Probiotic Strain Escherichia Coli 5C (ECP24®)) in the Prevention of Recurrent Cystitis in Menopausal Women: A Randomized, Double-Blind, Placebo-Controlled Clinical Trial
研究概览
详细说明
Recurrent cystitis, defined as two or more episodes within 6 months or three or more episodes within 12 months, is particularly frequent in menopausal women because of age-related changes in estrogen levels, the urogenital epithelium, and the microbiota. The gastrointestinal tract is considered an important reservoir of uropathogenic bacteria, and intestinal dysbiosis may contribute to recurrent urinary tract infections.
This study is a randomized, double-blind, placebo-controlled, parallel-group clinical trial designed to evaluate whether Colipral® (probiotic strain Escherichia coli 5C (ECP24®)) reduces the proportion of menopausal women experiencing recurrent symptomatic cystitis compared with placebo during a 24-week follow-up period. Recurrence is defined as the appearance of urinary symptoms compatible with the need for therapy and confirmed by urine culture.
A total of 134 menopausal women with recurrent cystitis will be enrolled and randomized in a 1:1 ratio to receive either Colipral® or placebo. Participants in the active treatment group will receive one capsule daily for 12 weeks, while participants in the control group will receive an identical placebo for the same duration. The follow-up period will continue beyond treatment discontinuation to evaluate the persistence of the preventive effect.
Secondary objectives include evaluation of the number of cystitis episodes, time to first recurrence, antibiotic consumption, urinary pain assessed by the Visual Analogue Scale (VAS), symptom severity, and quality of life assessed using the UTI-SIQ-8 questionnaire.
研究类型
注册 (估计的)
阶段
- 不适用
联系人和位置
学习联系方式
- 姓名:Alessandro Messina, MD
- 电话号码:011 56 16 111
- 邮箱:alessandro.messina@aslbi.piemonte.it
参与标准
资格标准
适合学习的年龄
- 成人
- 年长者
接受健康志愿者
描述
Inclusion Criteria:
- Menopausal female patients.
- Age between 55 and 70 years.
- Diagnosis of recurrent cystitis: ≥2 episodes in 6 months or ≥3 episodes in 12 months, with at least 1 documented episode from urine culture in the last 12 months (if available).
Exclusion Criteria:
- Complicated urinary tract infections (UTIs) or major complicating factors, including relevant anatomical abnormalities, catheterization, active calculosis, or significant immunosuppression.
- Hormone replacement therapy (HRT) that has been ongoing or discontinued for less than 6 months.
- Pyelonephritis within the past 6 months.
- Ongoing continuous antibiotic prophylactic therapy (or inability to suspend it).
- Chronic inflammatory bowel diseases (ulcerative colitis or Crohn's disease).
- Allergy to the probiotic or its excipients.
学习计划
研究是如何设计的?
设计细节
- 主要用途:预防
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:四人间
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
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实验性的:Colipral®
Participants will receive Colipral® at a dose of 1 capsule per day, administered in the morning or evening, for 12 weeks.
The study will evaluate the efficacy and safety of Colipral® in the prevention of recurrent cystitis in menopausal women.
|
Colipral® is a probiotic food supplement in gastro-resistant capsules containing the probiotic strain Escherichia coli 5C (ECP24®).
Participants will receive one capsule orally once daily, in the morning or evening, for 12 weeks.
|
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安慰剂比较:Placebo
Participants will receive placebo capsules identical in shape, color, and packaging to Colipral®, administered as 1 capsule per day in the morning or evening for 12 weeks.
|
Matching placebo identical in shape, color, and packaging to Colipral®, administered orally as one capsule daily in the morning or evening for 12 weeks.
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研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Proportion of Participants With at Least One Episode of Symptomatic Cystitis
大体时间:24 weeks
|
Proportion of participants with at least one episode of symptomatic cystitis during the 24-week follow-up period.
Each episode must meet clinical criteria and have microbiological confirmation by urine culture.
|
24 weeks
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Time to First Recurrence
大体时间:24 weeks
|
Time from randomization to the first episode of symptomatic cystitis confirmed by urine culture.
|
24 weeks
|
|
Number of Total Cystitis Episodes
大体时间:24 weeks
|
Total number of symptomatic cystitis episodes during the follow-up period.
|
24 weeks
|
|
Antibiotic Consumption
大体时间:24 weeks
|
Number of antibiotic cycles and total days of antibiotic therapy during follow-up.
|
24 weeks
|
|
Urinary Pain
大体时间:24 weeks
|
Urinary pain assessed using the Visual Analogue Scale (VAS).
|
24 weeks
|
|
Quality of Life and Symptom Severity
大体时间:24 weeks
|
Quality of life and symptom severity assessed using the UTI-SIQ-8 questionnaire.
|
24 weeks
|
合作者和调查者
研究记录日期
研究主要日期
学习开始 (估计的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
其他相关的 MeSH 术语
其他研究编号
- 388/CE, 09.06.2026
药物和器械信息、研究文件
研究美国 FDA 监管的药品
研究美国 FDA 监管的设备产品
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