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Evaluation of antibacterial peptide eye drops

Safety evaluation of eye drops containing antibacterial peptides in the treatment of infectious bacterial keratitis

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
IRCT
Registry ID
IRCT20181229042160N4
Enrollment
10
Registered
2023-12-24
Start date
2024-01-21
Completion date
Unknown
Last updated
2024-01-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bacterial keratitis. Keratitis

Interventions

Intervention 1: Control group: Treatment using standard antibiotic eye drops (ceftazidime + vancomycin). Intervention 2: Treatment is done using standard antibiotic eye drops (ceftazidime + vancomycin

Sponsors

Bagheiat-allah University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients with bacterial keratitis caused by Staphylococcus aureus or Pseudomonas aeruginosa Having consent to enter the study

Exclusion criteria

Exclusion criteria: The patient's lack of consent to continue the examinations Occurrence of any unusual side effects Infectious keratitis of fungal origin Spread of infection to other parts of the eye Having systemic immunodeficiency Having a cornea transplant

Design outcomes

Primary

MeasureTime frame
Keratitis infection. Timepoint: 3, 7, and 14 days after drug administration. Method of measurement: Microscopic evaluation using Slit lamp.;Treatment duration. Timepoint: 3, 7, and 14 days after drug administration. Method of measurement: Microscopic evaluation using Slit lamp.

Secondary

MeasureTime frame
Corneal opacity. Timepoint: 7, 14, 30 and 90 days. Method of measurement: Microscopic evaluation using Slit lamp.;Pain and burning. Timepoint: 7, 14, 30 and 90 days. Method of measurement: Microscopic evaluation using Slit lamp.;Shedding tears. Timepoint: Macroscopic and microscopic evaluation using Slit lamp. Method of measurement: 7, 14, 30 and 90 days.;Eye redness. Timepoint: 7, 14, 30 and 90 days. Method of measurement: Macroscopic and microscopic evaluation using Slit lamp.;Eye inflammation. Timepoint: 7, 14, 30 and 90 days. Method of measurement: Microscopic evaluation using slit lamp.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMehrdad Moosazadeh Moghaddam

Bagheiat-allah University of Medical Sciences

mm.genetics@gmail.com+98 21 8755 4808

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026