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临床试验/NCT03506256
NCT03506256Unknown4 期

Noroxin Efficacy and Safety Trial

OBS Pakistan0 个研究点目标入组 1,000 人开始时间: 2018年5月10日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
发起方
OBS Pakistan
入组人数
1,000
主要终点
Number of Patients treated with Noroxin (Efficacy)

研究概览

简要总结

To determine the efficacy and safety of Norfloxacin (Noroxin)

详细描述

Urinary tract infections (UTIs) are some of the most common bacterial infections, affecting 150 million people each year worldwide. Clinically, UTIs are categorized as uncomplicated or complicated. Uncomplicated UTIs typically affect individuals who are otherwise healthy and have no structural or neurological urinary tract abnormalities; these infections are differentiated into lower UTIs (cystitis) and upper UTIs (pyelonephritis). Several risk factors are associated with cystitis, including female gender, a prior UTI, sexual activity, vaginal infection, diabetes, obesity and genetic susceptibility.

UTIs are caused by both Gram-negative and Gram-positive bacteria, as well as by certain fungi. The most common causative agent for both uncomplicated and complicated UTIs is uropathogenic Escherichia coli (UPEC). For the agents involved in uncomplicated UTIs, UPEC is followed in prevalence by Klebsiella pneumoniae, Staphylococcus saprophyticus, Enterococcus faecalis, group B Streptococcus (GBS), Proteus mirabilis, Pseudomonas aeruginosa, Staphylococcus aureus and Candida spp. Currently, antibiotics - such as trimethoprim sulfamethoxazole, floxacin and ampicillin - are the most commonly recommended therapeutics for UTIs6. UTIs are becoming increasingly difficult to treat owing to the widespread emergence of an array of antibiotic resistance mechanisms. Of particular concern are members of the family Enterobacteriaceae, including E. coli and K. pneumoniae, which have both acquired plasmids encoding extended-spectrum β-lactamases (ESBLs). These plasmids rapidly spread resistance to third-generation cephalosporins as well as other antibiotics.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Written informed consent
  • At least one typical symptom of acute, lower urinary tract infection out of dysuria, frequency, macrohaematuria, cloudy or smelly urine or self-diagnosed cystitis

排除标准

  • Duration of UTI symptoms for more than 7 days before physician's visit
  • Clinical signs of invasiveness such as fever (axillary body temperature >38 degrees Celsius), costovertebral pain or tenderness, rigors, nausea or vomiting
  • Known or suspicion of anatomical or functional abnormality of the urinary tract
  • Vaginal symptoms: discharge, irritation
  • Diabetes mellitus
  • Immunosuppression (e.g. prednisone equivalent >10mg per day for >14 days, chemotherapy, radiotherapy, immunomodulators, HIV infection, neutropenia)
  • Any other serious comorbidity as judged by the treating physician
  • Bladder catheter in situ or during the past 30 days
  • Pregnancy
  • Recurrent urinary tract infection (more than 3 infections during the last 12 months)
  • Antibiotic treatment during the last 4 weeks

研究组 & 干预措施

Norofloxacin

Experimental

The recommended dosage of norfloxacin for urinary-tract infections in adults is 400 mg orally every 12 hours; the drug should be given for 7 to 10 days in uncomplicated infections and for 10 to 21 days in complicated ones. Adverse drug effects were mild and included disturbances of the gastrointestinal tract and the central nervous system. The study shall be completed in accordance with the ICH topic E6 (R1)(CPMP/ICH/one hundred thirty five/95) guiding principle for top medical practice and the ideas enunciated within the announcement of Helsinki and the approval by way of an Institutional Ethics Committee.

干预措施: Norfloxacin 400 MG (Drug)

结局指标

主要结局

Number of Patients treated with Noroxin (Efficacy)

时间窗: 14 Days

To evaluate efficacy of Norfloxacin by measuring clinical response, the resolution of sign and symptoms of post-therapy as compared to start of therapy

次要结局

  • Number of Adverse Effects with Noroxin (Safety)(14 Days)

研究者

发起方
OBS Pakistan
申办方类型
Industry
责任方
Sponsor

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