Clinical Trial

Clinical Effectiveness of a Once-daily Regimen of Tigecycline Compared to the Standard Regimen

Active, Not Recruiting Phase 4
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Record status
This record was last updated December 2, 2025 (before its estimated February 1, 2026 completion). Its status may not reflect the trial's current state.
Summary
To compare the clinical response (efficacy) and the safety of the tigecycline once daily regimen versus the standard regimen (twice daily regimen). Clinical response was categorized as a cure, failure of treatment, or indeterminate outcome.24 Treatment success (Cure): defined as resolution of signs/symptoms of infection, microbiological cure (negative cultures after tigecycline use), improvement of infection markers (leukocytic count, C reactive protein, and procalcitonin). Treatment failure: defined as persistence of signs/symptoms of infection despite antimicrobial therapy, deterioration of infection markers (leukocytic count, C reactive protein, and Procalcitonin). Indeterminate response: subjects who do not have an outcome determination for reasons unrelated to the study drug or infection (e.g., loss to follow-up, withdrawal of consent, etc.) Safety will be assessed by the incidence of adverse events especially which leads to treatment discontinuation.36
Trial Details
NCT Number NCT07258225
Lead Sponsor Air Force Specialized Hospital, Cairo, Egypt
Conditions Multi Drug Resistant Infections
Enrollment 86 participants
Start Date 2024-04-01
Primary Completion 2026-02-01 (estimated)
Study Completion 2026-04-30 (estimated)
Updated on ClinicalTrials.gov 2025-12-02