The Antibiogram and Outcomes of Antimicrobial Regimens in Microbial Keratitis: A Prospective Cohort Study

NCT05655689 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 123

Last updated 2024-01-25

No results posted yet for this study

Summary

This study is an observational prospective cohort study which aims to generate an antibiogram and to assess the clinical responses and outcomes of microbial keratitis patients, treated with empiric topical antimicrobial therapies, with the main objective being to recommend the most effective empiric therapy. Microbial keratitis patients are attending the Cornea Outpatient Clinic at Alexandria Main University Hospital, Alexandria, Egypt.

Conditions

  • Bacterial Keratitis
  • Fungal Keratitis
  • Mixed Bacterial and Fungal Keratitis
  • Microbial Keratitis

Interventions

DRUG

Moxifloxacin Ophthalmic 0.5% Ophthalmic Solution

In the observational study, patients treated with topical antibiotic moxifloxacin 0.5% eye drops as part of routine medical care are observed. The investigator does not assign any specific intervention to the study participants.

DRUG

Ceftazidime 5% + vancomycin 5%

In the observational study, patients treated with topical fortified antibiotics ceftazidime 5% and vancomycin 5% eye drops as part of routine medical care are observed. The investigator does not assign any specific intervention to the study participants.

DRUG

Gentamicin 1.4% + vancomycin 5%

In the observational study, patients treated with the topical fortified antibiotics gentamicin 1.4% and vancomycin 5% eye drops as part of routine medical care are observed. The investigator does not assign any specific intervention to the study participants.

DRUG

Natamycin 5% Oph Susp

In the observational study, patients treated with the topical natamycin 5% antifungal eye drops as part of routine medical care are observed. The investigator does not assign any specific intervention to the study participants.

DRUG

Voriconazole 1%

In the observational study, patients treated with voriconazole 1% antifungal eye drops as part of routine medical care are observed. The investigator does not assign any specific intervention to the study participants.

DRUG

Natamycin 5% + voriconazole 1%

In the observational study, patients treated with the topical natamycin 5% and voriconazole 1% antifungals eye drops as part of routine medical care are observed. The investigator does not assign any specific intervention to the study participants.

DRUG

Natamycin 5%+ ceftazidime 5% + vancomycin 5%

In the observational study, patients treated with the topical natamycin 5% and antifungal and the fortified antibiotic ceftazidime 5% and vancomycin 5% eye drops as part of routine medical care are observed. The investigator does not assign any specific intervention to the study participants.

DRUG

Voriconazole 1% + ceftazidime 5% + vancomycin 5%

In the observational study, patients treated with the topical voriconazole 1% antifungal and the fortified antibiotics ceftazidime 5% and vancomycin 5% eye drops as part of routine medical care are observed. The investigator does not assign any specific intervention to the study participants.

Sponsors & Collaborators

  • Alexandria University

    lead OTHER

Principal Investigators

  • Nelly M Mohamed, PhD · Associate Professor of Microbiology and Immunology, Alexandria University

  • Tamer H Massoud, PhD · Associate Professor of Ophthalmology, Alexandria University

  • Noha A Hamdy, PhD · Assistant Professor of Clinical Pharmacy, Alexandria University

  • Amira A Nayel, PharmD · Master's student at the Department of Clinical Pharmacy and Pharmacy Practice, Alexandria University

Eligibility

Min Age
1 Year
Max Age
90 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-12-31
Primary Completion
2023-01-01
Completion
2023-01-01

Countries

  • Egypt

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05655689 on ClinicalTrials.gov