Characterization of the Synergistic Antibacterial Effect of Verapamil on Bacterial Isolates From Cancer Patients

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-90
SponsorAssiut University

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 volunteers

Qualifiers

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

Design model

Other

Time perspective

Prospective

Treatments tested in this trial

  • verapamil

    Drug

    Intervention 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

No treatment groups listed

Trial outcomes

Primary outcomes

1

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

Time frame
Baseline

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

This trial is not recruiting at the moment. You can still explore other options: