About this trial
Multidrug-resistant (MDR) bacteria represent a significant global health challenge, particularly among immunocompromised populations such as cancer patients undergoing chemotherapy. These patients are highly susceptible to severe infections due to weakened immune defenses, often necessitating the use of broad-spectrum or combination antibiotic therapy. Combination regimens may enhance treatment efficacy through synergistic effects, helping to overcome bacterial resistance mechanisms and improve clinical outcomes.
In recent years, there has been growing interest in the use of non-antibiotic drugs as adjunctive agents to enhance antimicrobial activity. These agents, often referred to as antibiotic adjuvants or resistance modifiers, may improve antibiotic effectiveness through mechanisms such as inhibition of bacterial efflux pumps, disruption of biofilm formation, or interference with resistance pathways.
Verapamil, a widely used calcium channel blocker, has demonstrated potential antimicrobial and resistance-modifying properties. Experimental evidence suggests that verapamil can inhibit bacterial efflux pumps, thereby increasing intracellular concentrations of antibiotics and enhancing their activity against resistant organisms.
This study aims to evaluate the in vitro synergistic antibacterial activity of verapamil in combination with selected antibiotics against MDR, extensively drug-resistant (XDR), and pandrug-resistant (PDR) bacterial isolates obtained from cancer patients. Standard microbiological methods will be used to determine antimicrobial susceptibility and minimum inhibitory concentrations, while combination effects will be assessed using established synergy testing approaches.
The findings of this study may contribute to identifying novel, cost-effective strategies to combat antimicrobial resistance through drug repurposing and optimization of existing antibiotic therapies.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
MDR: resistant to one or more agent within three or more of antimicrobial classes
XDR: resistant to one or more agent within all but two antimicrobial classes
PDR: resistant to all agents within all antimicrobial classes.
Disqualifiers
Bacterial isolates from non-cancer patients.
Contaminant or non-pathogenic isolates.
Duplicate isolates from the same patient with identical antibiogram.
Bacterial isolates that are neither MDR, XDR OR PDR.
Trial population
The study will be carried out on clinical specimens of cancer patients already withdrawn for routine testing during the study period
Trial design
Other
Prospective
Treatments tested in this trial
verapamil
DrugIntervention Name: Verapamil Other Names: Verapamil hydrochloride Clinical specimens from cancer patients collected for routine testing will be included. Bacterial isolates will be cultured on appropriate media and identified using standard microbiological methods and/or automated systems. Antimicrobial susceptibility testing will be performed using the Kirby-Bauer disk diffusion method or automated systems according to CLSI 2025 guidelines. A stock solution of verapamil will be prepared under aseptic conditions. The antibacterial activity of selected antibiotics alone and in combination with verapamil will be evaluated. Minimum inhibitory concentrations (MICs) will be determined using the broth microdilution method. Synergistic interactions will be assessed using the checkerboard method and quantified by fractional inhibitory concentration index (FICI).
Treatment groups
Trial outcomes
Primary outcomes
Characterization of the synergistic antibacterial effect of Verapamil on bacterial isolates from patients in South Egypt Cancer Institute
Determination of the antibiotic sensitivity patterns of the bacterial isolates as measured by MIC values
Locations
Sponsors and contacts
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