EUCTR2015-003487-36-GB进行中(未招募)1 期
Alternatives to prophylactic antibiotics for the treatment of recurrent urinary tract infection in women - ALTAR
适应症
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中(未招募)
- 入组人数
- 240
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- Female
入选标准
- •Women aged 18 years and over.
- •Women with rUTI who, in consultation with a clinician, have decided that prophylaxis is an appropriate option (to include women who have suffered at least three episodes of symptomatic UTI within the preceding 12 months or two episodes in the last 6 months or a single severe infection requiring hospitalisation).
- •Able to take a once daily oral dose of at least one of nitrofurantoin, or trimethoprim, or cephalexin.
- •Able to take Methenamine hippurate.
- •Women who agree to take part in the trial but who are already taking Methenamine or antibiotic prophylaxis will be consented for participation and will stop their preventative therapy for a 3-month washout period. They will then be reassessed and if still eligible undergo baseline assessment and randomisation.
- •Able to give informed consent for participation in trial.
- •Able and willing to adhere to an 18-month study period.
- •Are the trial subjects under 18? no
- •Number of subjects for this age range: 0
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 200
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 40
排除标准
- •Women unable to take Methenamine hippurate e.g. known allergy to Methenamine hippurate, severe hepatic impairment (Childs –Pugh class C, score of 10 or more, see appendix 4), gout, eGFR < 10 ml/min, Proteus sp. as consistent proven causative organism for rUTIs.
- •Women who are unable to take nitrofurantoin and trimethoprim and cephalexin.
- •Women with correctable urinary tract abnormalities that are considered to be contributory to the occurrence of rUTI.
- •Presence of symptomatic UTI – this will be treated and symptoms resolved prior to randomisation.
- •Pregnancy or intended pregnancy in next 12 months.
- •Women who are breast feeding.
- •Women already taking methenamine or antibiotic prophylaxis and declining a 3-month washout period.
研究者
相似试验
尚未招募
Unknown
comparison of antibiotics in elective caesarean sectioCTRI/2024/08/072337Dr NEHA SINGH
已完成
不适用
To study whether giving long duration prophylactic antibiotics in patients with isolated blunt chest injuries managed with intercostal tube drainage (ICD) has any role in preventing ICD related infectious complications.CTRI/2019/10/021704Department of Trauma surgery120
已完成
不适用
Impact of Antibiotic Prophylaxis in Per-oral Endoscopic Myotomy for Esophageal Motor DisordersEsophagus DisorderEsophageal AchalasiaNCT03944863Société Française d'Endoscopie Digestive252
进行中(未招募)
1 期
Pervention and Intervention of infections following Caesarean SectioSub-study 1: women delivering a child by caesarean section Sub-study 2: Women, who are hospitalized at the obstetrical ward for reoperation because of superficial or deep infection or haematoma after caesarean sectionEUCTR2012-002068-29-DKJan Stener Joergensen2,844
尚未招募
Unknown
A study comparing the patients who were given and those who were not given prophylacyic antibiotics before a planned laparoscopic gallbladder surgeryCTRI/2024/07/071617Regional Institute of Medical Sciences
