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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04168099
Other study ID # SBP new treatment
Secondary ID
Status Recruiting
Phase Phase 3
First received
Last updated
Start date December 1, 2018
Est. completion date December 30, 2028

Study information

Verified date November 2019
Source Tanta University
Contact Sherief Abd-Elsalam, ass. prof.
Phone 00201147773440
Email sheriefabdelsalam@yahoo.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

oral Gemifloxacin versus intravenous Cefotaxime in treatment of spontaneous bacterial peritonitis


Description:

Comparative Study between the Efficacy of oral Gemifloxacin and intravenous Cefotaxime in treatment of spontaneous bacterial peritonitis


Recruitment information / eligibility

Status Recruiting
Enrollment 60
Est. completion date December 30, 2028
Est. primary completion date December 1, 2028
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patients with spontaneous bacterial peritonitis

Exclusion Criteria:

- secondary peritonitis

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Cefotaxime
Cefotaxime IV
Gemifloxacin
Gemifloxacin oral

Locations

Country Name City State
Egypt Sherief Abd-Elsalam Tanta

Sponsors (1)

Lead Sponsor Collaborator
Tanta University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of patients with resolution of infection the total number of patients with resolution of infection 6 months
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