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Clinical Trials in India / NCT07807150
Starting soon Phase 3

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

NCT07807150 · tracked via the Priya Life Science India tracker
Sponsor
Post Graduate Institute of Medical Education and Research, Chandigarh
Phase
Phase 3
Started
2026-09-04
Last updated
2026-09-10

Condition(s) studied

Liver AbscessAmoebic Liver Abscess

Investigational drug(s) / intervention(s)

Diloxanide furoatePlacebo

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

Placebo: matched placebo 1 tab TDS for 10 days

Study summary

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.

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
No
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

Primary outcome measure(s)

Trial sites (1)

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

More Post Graduate Institute of Medical Education and Research, Chandigarh trials in India

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07807150 on ClinicalTrials.gov ↗ ← All trials in India