Norfloxacin With Itopride Versus Norfloxacin in Secondary Prophylaxis of Spontaneous Bacterial Peritonitis
NCT ID: NCT04161768
Last Updated: 2019-11-13
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
PHASE3
80 participants
INTERVENTIONAL
2018-12-01
2028-12-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
QUADRUPLE
Study Groups
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Norfloxacin
Norfloxacin 400 mg daily
Norfloxacin
Norfloxacin 400 mg daily
Norfloxacin and Itopride
Norfloxacin 400 mg daily and Itopride 50 mg three times daily.
Norfloxacin
Norfloxacin 400 mg daily
Itopride
Itopride 50 mg three times daily
Interventions
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Norfloxacin
Norfloxacin 400 mg daily
Itopride
Itopride 50 mg three times daily
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
ALL
No
Sponsors
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Tanta University
OTHER
Responsible Party
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Sherief Abd-Elsalam
Ass. Prof. Tropical Medicine
Principal Investigators
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Afaf Younes Mohammed Younes, Msc
Role: PRINCIPAL_INVESTIGATOR
Tanta University - Faculty of Medicine
Mona Ahmed Helmy Shehata, Prof.
Role: PRINCIPAL_INVESTIGATOR
Tanta University - Faculty of Medicine
Sherief Abd-Elsalam, Ass. Prof.
Role: PRINCIPAL_INVESTIGATOR
Tanta University - Tropical Medicine Department
Locations
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Sherief Abd-Elsalam
Tanta, , Egypt
Countries
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Central Contacts
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Facility Contacts
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Sherief Abd-Elsalam
Role: primary
Other Identifiers
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SBP Management
Identifier Type: -
Identifier Source: org_study_id
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