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NCT Number: NCT07807150

Efficacy of Diloxanide Furoate as Additional Luminal Agent Along With Metronidazole for the Treatment of Amoebic Liver Abscess

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 (1). 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 (2). 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 (3). Frequent relapses have been seen in ALA after treatment with metronidazole (4,5). As per literature, Diloxanide furoate eradicates intraluminal cysts in approximately 85-95% of patients with non-invasive amoebiasis (6).

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Post Graduate Institute of Medical Education and Research, Chandigarh, India

Chandigarh, 160012, India

Location contact

Deba Prasad Dhibar, MD

CONTACT

[email protected]

+911722756670

About this study

STUDY DESIGN: Prospective, randomised controlled, double blinded, clinical trial Population(P): Patients with newly diagnosed amoebic liver abscess presenting to Post graduate Institute of Medical Education and Research, Chandigarh Intervention(I): Diloxanide furoate plus Metronidazole therapy Comparison(C): Metronidazole monotherapy plus placebo Outcome(O): Clinical cure rate, parasite clearance and recurrence rate at 8 weeks follow up Time(T): September 2026 to July 2027

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age >18 years 2. Male or Female 3. 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 -

Treatment and study plan

Diloxanide furoate

Drug

Diloxanide furoate group will receive oral Diloxanide furoate 500mg 1 tab TDS for 10 days

Other names: Standard care of Metronidazole i.e. intravenous 750mg TDS or oral 800mg 1 tab TDS for 14 days.

Placebo

Other

matched placebo 1 tab TDS for 10 days

Other names: Standard care of Metronidazole i.e. intravenous 750mg TDS or oral 800mg 1 tab TDS for 14 days.

Primary outcomes

  1. Clinical cure

    Time frame: 8 weeks

    "Clinical cure" is defined as 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.

  2. Treatment failure

    Time frame: 8 weeks

    "Treatment failure" is defined as the fulfilling of any one or more of the following conditions:

    • Persistently symptomatic even after 72 h of antimicrobial therapy and percutaneous aspiration or drainage of the hepatic collection
    • Emergence of new collection in the liver during the course of antimicrobial therapy
    • Emergence of shock and or new onset organ failure (Encephalopathy, ARDS, AKI, MODS) during the course of therapy

    e. Patients requiring persistent drainage or repeated aspiration of the abscess even after 4 weeks of antimicrobial therapy

Secondary outcomes

  1. 1. Parasitic clearance

    Time frame: 8 weeks

    Stool EH DNA PCR becomes negative after initial positive test at 2 & 8 weeks.

  2. Recurrence of liver abscess

    Time frame: 8 weeks

    Occurrence of new liver abscess after achieving clinical cure during 8 weeks of follow up.

  3. Duration of the therapy

    Time frame: 8 weeks

    Number of days of antimicrobial therapy required to achieve clinical cure

  4. Adverse drug reaction (ADR)

    Time frame: 8 weeks

    Incidence of adverse drug reaction related to the ongoing antimicrobial therapy.

Study contacts

Contact information is provided by the study sponsor or research team.

Deba Prasad Dhibar, MD

CONTACT

[email protected]

+911722756670

HARLEEN SOOD, MD

CONTACT

[email protected]

+911722756670

Sponsors and collaborators

Lead sponsor

Post Graduate Institute of Medical Education and Research, Chandigarh

Other

Registry information

Official study title

Efficacy of Diloxanide Furoate as Additional Luminal Agent Along With Metronidazole for the Treatment of Amoebic Liver Abscess: A Randomized Controlled Clinical Trial

Acronym: DFALA RCT

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Sep 8, 2026
Registry last updated
Sep 8, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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