Efficacy of Diloxanide Furoate as Additional Luminal Agent Along With Metronidazole for the Treatment of Amoebic Liver Abscess (DFALA RCT)
Efficacy of Diloxanide Furoate as Additional Luminal Agent Along With Metronidazole for the Treatment of Amoebic Liver Abscess: A Randomized Controlled Clinical Trial
Liver abscess is a common cause of presentation to medical emergency. Among the various causes of liver abscess, Amoebic liver abscess (ALA) is a frequent cause that can resemble pyogenic infections in tropical regions. Prompt diagnosis and empirical antimicrobials along with drainage or aspiration produces successful clinical recovery.
Metronidazole has been the cornerstone of ALA therapy and achieves clinical cure in approximately 90% of uncomplicated cases. It is active against both luminal and tissue forms of Entamoeba histolytica, however it has relatively limited effect against the intestinal (luminal) form of parasite, so intestine may remain colonized after apparent resolution. This persistent intestinal carriage can lead to relapse or ongoing transmission. This prompts physicians to consider Diloxanide furoate as additional luminal agent for treatment of ALA along with metronidazole therapy.
Diloxanide furoate is traditionally administered after metronidazole to eradicate residual intestinal infection and lower relapse rates. However, many patients receive only metronidazole because of cost, limited awareness about luminal therapy, poor adherence, or absence of local comparative evidence. Studies have shown that 30-40% of patients can have inadequate luminal parasite clearance following standard metronidazole therapy for ALA. Frequent relapses have been seen in ALA after treatment with metronidazole. As per literature, Diloxanide furoate eradicates intraluminal cysts in approximately 85-95% of patients with non-invasive amoebiasis.
It remains unclear whether giving Diloxanide furoate at the same time as Metronidazole has any additional benefit compared with Metronidazole alone for patients with ALA. Theoretically, addition of diloxanide furoate could increase overall cure rate, rapid parasite clearance and reduce recurrence.
However, there is no randomized controlled trial available at present to address the research question whether dual therapy with Diloxanide furoate with Metronidazole has any added benefits in ALA. So, this randomized controlled trial has been planned to evaluate whether adding Diloxanide furoate to Metronidazole treatment improves outcomes. This study will generate robust data to formulate/modify the existing guidelines of management of ALA especially in endemic areas.
Research question:
Whether addition of Diloxanide furoate with Metronidazole is more efficacious than Metronidazole monotherapy for treatment of amoebic liver abscess in terms of achieving better clinical cure, parasitic clearance and reduced recurrence.
研究概览
详细说明
研究类型
注册 (估计的)
阶段
- 第三阶段
联系人和位置
学习联系方式
- 姓名:Deba Prasad Dhibar, MD
- 电话号码:+911722756670
- 邮箱:drdeba_prasad@yahoo.co.in
研究联系人备份
- 姓名:HARLEEN SOOD, MD
- 电话号码:+911722756670
- 邮箱:harleen.sood@gmail.com
学习地点
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Chandigarh
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Chandigarh、Chandigarh、印度、160012
- Post Graduate Institute of Medical Education and Research, Chandigarh, India
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接触:
- Deba Prasad Dhibar, MD
- 电话号码:+911722756670
- 邮箱:drdeba_prasad@yahoo.co.in
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-
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:
- Age >18 years
- Male or Female
- Patients with newly diagnosed amoebic liver abscess
Exclusion Criteria:
- Patients not able to take orally
- Patients receiving antimicrobials for more than 72 hours before the enrolment in the study
- History of hypersensitivity reactions to Metronidazole or Diloxanide furoate
- Pregnancy
- Patients on antiplatelets/anticoagulation within 4 weeks of presentation
- Presentation with shock (SBP<90 and/ or DBP< 60 mmHg)
- Patients with ARDS (SpO2 ≤92%, PaO2/Fio2<300, requiring oxygen therapy)
- Patients with renal dysfunction / CKD (Creatinine >1.5mg/dl)
- Patients with altered sensorium (GCS <15)
- Patients with known malignancy
- Patients with HIV
- Not willing for informed consent
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:三倍
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
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实验性的:Diloxanide furoate group
Diloxanide furoate group will receive oral Diloxanide furoate 500mg 1 tab TDS for 10 days plus standard care of Metronidazole i.e. intravenous 750mg TDS or oral 800mg 1 tab TDS for 14 days.
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Diloxanide furoate group will receive oral Diloxanide furoate 500mg 1 tab TDS for 10 days
其他名称:
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安慰剂比较:Placebo group
Will receive matched placebo 1 tab TDS for 10 days plus stand care of Metronidazole i.e. intravenous 750mg TDS or oral 800mg 1 tab TDS for 14 days.
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matched placebo 1 tab TDS for 10 days
其他名称:
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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 |
|---|---|---|
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Clinical cure
大体时间:8 weeks
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"Clinical cure" is defined as number of participants becoming asymptomatic with fever resolution for ≥48 hours, including USG demonstrating no drainable collection in the liver along with removal of the pigtail catheter if any.
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8 weeks
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Treatment failure
大体时间:8 weeks
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"Treatment failure" is defined as the number of participants fulfilling of any one or more of the following conditions:
e. Patients requiring persistent drainage or repeated aspiration of the abscess even after 4 weeks of antimicrobial therapy |
8 weeks
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Duration of the therapy
大体时间:8 weeks
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Number of days of antimicrobial therapy required to achieve clinical cure
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8 weeks
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Adverse drug reaction (ADR)
大体时间:8 weeks
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Incidence of adverse drug reaction related to the ongoing antimicrobial therapy.
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8 weeks
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1. Parasitic clearance
大体时间:8 weeks
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Number of participant's Stool EH DNA PCR becomes negative after initial positive test at 2 & 8 weeks.
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8 weeks
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Recurrence of liver abscess
大体时间:8 weeks
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Number of participants with occurrence of new liver abscess after achieving clinical cure during 8 weeks of follow up.
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8 weeks
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合作者和调查者
出版物和有用的链接
一般刊物
- Chavez-Tapia NC, Hernandez-Calleros J, Tellez-Avila FI, Torre A, Uribe M. Image-guided percutaneous procedure plus metronidazole versus metronidazole alone for uncomplicated amoebic liver abscess. Cochrane Database Syst Rev. 2009 Jan 21;2009(1):CD004886. doi: 10.1002/14651858.CD004886.pub2.
- Sharma N, Sharma A, Varma S, Lal A, Singh V. Amoebic liver abscess in the medical emergency of a North Indian hospital. BMC Res Notes. 2010 Jan 25;3:21. doi: 10.1186/1756-0500-3-21.
- Blessmann J, Binh HD, Hung DM, Tannich E, Burchard G. Treatment of amoebic liver abscess with metronidazole alone or in combination with ultrasound-guided needle aspiration: a comparative, prospective and randomized study. Trop Med Int Health. 2003 Nov;8(11):1030-4. doi: 10.1046/j.1360-2276.2003.01130.x.
- Kumar R, Patel R, Priyadarshi RN, Narayan R, Maji T, Anand U, Soni JR. Amebic liver abscess: An update. World J Hepatol. 2024 Mar 27;16(3):316-330. doi: 10.4254/wjh.v16.i3.316.
- Stanley SL Jr. Amoebiasis. Lancet. 2003 Mar 22;361(9362):1025-34. doi: 10.1016/S0140-6736(03)12830-9.
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
- IEC-INT/2026/DM-4109
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
IPD 计划说明
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研究美国 FDA 监管的药品
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