Actively Recruiting

Phase 3
All Genders
NCT04161768

Norfloxacin With Itopride Versus Norfloxacin in Secondary Prophylaxis of Spontaneous Bacterial Peritonitis

Led by Tanta University · Updated on 2019-11-13

80

Participants Needed

1

Research Sites

521 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Norfloxacin versus Norfloxacin with Itopride in Secondary Prophylaxis of Spontaneous Bacterial Peritonitis

CONDITIONS

Official Title

Norfloxacin With Itopride Versus Norfloxacin in Secondary Prophylaxis of Spontaneous Bacterial Peritonitis

Who Can Participate

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Cirrhotic patients with ascites who had previous episodes of spontaneous bacterial peritonitis (SBP).
Not Eligible

You will not qualify if you...

  • Allergy or contraindication for the study drugs.
  • Recent antibiotic therapy within the previous 2 weeks.
  • Presence of hepatocellular carcinoma or other cancers.
  • Pregnancy or lactation.

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Sherief Abd-Elsalam

Tanta, Egypt

Actively Recruiting

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Research Team

S

Sherief Abd-Elsalam, ass. prof.

CONTACT

S

sherief abd-elsalam, ass. prof.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

QUADRUPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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