A comparison of concomitant administration of Azithromycin and Cefixime to Azithromycin alone in the treatment of Typhoid
试验速览
- 阶段
- 4 期
- 状态
- 尚未招募
- 入组人数
- 1,500
- 试验地点
- 2
- 主要终点
- Clinical failure and Microbiological failure
研究概览
简要总结
Typhoidand paratyphoid (enteric) fever affects more than 11 million children andadults globally each year including 7 million in South Asia. Up to 1% ofpatients who get typhoid may die of the disease and,in those that survive,aprolonged period of ill health and catastrophic financial cost to the familymay follow. In the last 20 years, treatment of typhoid fever with a 7-daycourse of a single oral antimicrobial,such as ciprofloxacin, cefixime orazithromycin, given in an out-patient setting has led to patient recovery in 4to 6 days without the need for expensive hospitalization. Increasing antimicrobialresistance in Asia and sub-Saharan Africa threatens the effectiveness of these treatments and increases the risk of prolonged illness and severe disease. The recentemergence of a particularly resistant typhoid strain in Pakistan, andsubsequent international spread, adds urgency to this problem andSalmonellaisnow listed as a high(Priority 2) pathogen by WHO.
Treatment with combinations of antimicrobials may be moreeffective for treating typhoid fever and mitigate the problems of resistance.This suggestion is based on expert opinion but not backed up by good qualityevidence. The ACT-South Asia study aims to compare a combination ofazithromycin and cefixime with azithromycin alone in the outpatient treatmentof clinically suspected and confirmed uncomplicated typhoid fever. We willrecruit 1500 patients across sites in Bangladesh, India, Nepal and Pakistan. Aplacebo (sugar pill) will be used instead of cefixime in the single drug arm sothat neither the patient nor the study team know which patient is receivingwhich treatment. We will assess whether treatment outcomes are better with thecombination after one week of treatment and at one and three month follow-up.Both antimicrobials are widely used and have excellent safety profiles. If thecombination treatment is better than the single antibiotic treatment, this willbe an important result for patients across South Asia and other typhoid endemicareas. We will additionally investigate the financial implications for familiesand health system.
研究设计
- 研究类型
- Interventional
- 分配方式
- Computer generated randomization
- 盲法
- Participant, Investigator and Outcome Assessor Blinded
入排标准
- 年龄范围
- 2.00 Year(s) 至 65.00 Year(s)(—)
- 性别
- All
入选标准
- •A history of fever at presentation for 72 hours or more and a documented fever (37.5 degrees Celsius or more(axillary) or 38degree Celsius or more(oral))
- •Age 2 years or more (and weight 10kg and more) to 65 years 3.No clear focus of infection on initial clinical evaluation
- •Malaria RDT negative; dengue NS1 RDT negative; scrub typhus RDT negative; CRP rapid test 10 mg/L or more
- •Able to take oral treatment
- •Able to attend for follow-up and can be contacted by telephone
- •Written fully informed consent to participate in the study including assent for children in addition to parental/legal guardian consent.
排除标准
- •History of fever for >14 days
- •Pregnant or positive pregnancy test or breast-feeding
- •Presence of clinical symptoms or signs indicating a focal infection such as pneumonia; urinary infection, meningitis, eschar
- •Obtundation, hemodynamic shock, visible jaundice, gastrointestinal bleeding or any signs of severe disease that may require immediate hospitalization
- •Being treated for TB or HIV or severe acute malnutrition
- •Patients with cardiac disease
- •Previous history of hypersensitivity to any of the treatment options
- •Either of the trial drugs are contraindicated for any reason (e.g. drug interactions)
- •Has received azithromycin or cefixime in the last five days
- •Receiving another antimicrobial and responding clinically to the treatment as judged by the attending clinician.
- •Being on another drug ( for example certain kinds of antidepressants, or anticonvulsants) that may also cause prolonged QT interval
- •PCR positive for Co-Vid 19 before or after randomization.
结局指标
主要结局
Clinical failure and Microbiological failure
时间窗: 28 days
次要结局
- Fever clearance time(Under observation following the initiation of treatment)
- Time to treatment failure(Under observation following the initiation of treatment)
- Occurrence of adverse events in each treatment arm(Under observation following the initiation of treatment)
- Clearance of faecal carriage(One and three month follow-up visit)
- cost-effectiveness of the treatment in(Initiation of treatment and one month follow-up visit)
