Could a once-daily antibiotic dose beat the standard twice-daily regimen in ICU?
NCT ID NCT07258225
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study compares a once-daily dose of the antibiotic tigecycline to the usual twice-daily schedule in 86 critically ill adults with multidrug-resistant infections. The goal is to see if the simpler regimen works just as well or better at clearing the infection and reducing side effects. Participants are in the ICU and must be 18 or older with certain infections like pneumonia or skin infections.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
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About 86 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Apr 2024
- Expected to finish
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Apr 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Age 18 years or older. * Both males and females. * Diagnosis of infection has been established and tigecycline use is indicated (intra-abdominal, community-acquired pneumonia, skin Infections) or based on genetic testing and microbiological cultures (MDR Acinetobacter, MDR Stenotrophomonas, MDR Enterobacteriaceae, etc.) Exclusion Criteria: * Pregnancy and lactation. * Bloodstream infections (BSI) and urinary tract infections (UTIs). * Refusal of attending staff or patient, or family. * Contraindications to tigecycline, such as hypersensitivity and allergy. * Patients receiving ≤ 1 day of tigecycline (insufficient length of therapy). * Patients who have acute physiology and chronic health evaluation (APACHE 2) score of more than 35 (high risk of mortality). * Do not resuscitate/do not intubate (DNR, DNI) patients.
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Air force specialized hospital
Cairo, Cairo Governorate, 11765, Egypt
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