Actively Recruiting

Phase 3
Age: 18Years +
All Genders
NCT04168099

Oral Gemifloxacin Versus Intravenous Cefotaxime in Treatment of Spontaneous Bacterial Peritonitis

Led by Tanta University · Updated on 2019-11-19

60

Participants Needed

1

Research Sites

526 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

oral Gemifloxacin versus intravenous Cefotaxime in treatment of spontaneous bacterial peritonitis

CONDITIONS

Official Title

Oral Gemifloxacin Versus Intravenous Cefotaxime in Treatment of Spontaneous Bacterial Peritonitis

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients with spontaneous bacterial peritonitis
Not Eligible

You will not qualify if you...

  • Secondary peritonitis

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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3
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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

TREATMENT

Number of Arms

2

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