Host Response to Urinary Tract Infection in Women
研究概览
地位
条件
详细说明
Procedures subjects will undergo once they have read and signed the consent are:
Questions about their medical and sexual history and current symptoms of urinary tract infection. They will be asked to provide a clean catch urine sample. We will collect periurethral, vaginal and rectal swabs. Blood will collected. They will be given a diary to take home and record all episodes of sexual intercourse, contraceptive use, vaginal and urinary symptoms and medication use.
They will be given standard treatment for the current urinary tract infection. Follow-up visits will be scheduled 2 weeks,one month,two month and three month after initial visit.
研究类型
注册 (实际的)
联系人和位置
学习地点
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Washington
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Seattle、Washington、美国、98195
- University of Washington/Hall Health Primary Care Center
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参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
取样方法
研究人群
描述
Inclusion Criteria:
- Female
- Age 18-49 years
- Able to provide written informed consent
- diagnosis of acute cystitis with symptoms for fewer than 7 days
Exclusion Criteria:
- Not pregnant or planning pregnancy in next 3 months
- No chronic illness requiring medical supervision (e.g. diabetes mellitus)
- No known anatomic or functional abnormalities of the urinary tract
- No signs or symptoms suggestive of pyelonephritis (flank pain or tenderness, temperature over 100 degrees F, nausea or vomiting)
学习计划
研究是如何设计的？
设计细节
队列和干预
团体/队列 |
|---|
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Host
Women with current symptoms of a urinary tract infection
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研究衡量的是什么？
主要结果指标
结果测量 |
大体时间 |
|---|---|
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Determine elements of the immune response that may predispose a woman to recurrent urinary tract infection
大体时间：2017
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2017
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合作者和调查者
调查人员
- 首席研究员：Ann E Stapleton, M.D.、University of Washington
研究记录日期
研究主要日期
学习开始
初级完成 (实际的)
研究完成 (实际的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (估计)
研究记录更新
最后更新发布 (估计)
上次提交的符合 QC 标准的更新
最后验证
更多信息
此信息直接从 clinicaltrials.gov 网站检索，没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求，请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改，我们的网站上也会自动更新.