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Effect of Sodium Chloride 5% Solution as an Adjuvant Treatment With Antimicrobial Therapy in the Treatment of Bacterial Infectious Keratitis

Effect of Sodium Chloride 5% Solution as an Adjuvant Treatment With Antimicrobial Therapy in the Treatment of Bacterial Infectious Keratitis

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07452588
Acronym
keratitis
Enrollment
40
Registered
2026-03-05
Start date
2026-02-01
Completion date
2027-02-01
Last updated
2026-03-05

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

Conditions

Adjuvant Treatment Bacterial Infectious Keratitis, Infectious Keratitis, Sodium Chloride 5% Solution

Keywords

Bacterial infectious keratitis, Sodiunchloride5%

Brief summary

This study aims to detect the effect of sodium chloride 5% solution as an adjuvant treatment with antimicrobial therapy in treatment of bacterial infectious keratits and to assess whether NaCl 5% accelerates epithelial healing, improves microbial eradication, and enhances visual outcomes in bacterial infectious keratitis.

Detailed description

Prospective randomized control study to detect the effect of sodium chloride 5% solution as an adjuvant treatment with antimicrobial therapy in treatment of bacterial infectious keratits and to assess whether NaCl 5% accelerates epithelial healing, improves microbial eradication, and enhances visual outcomes in bacterial infectious keratitis.Data study will include two groups classified as follow : the first group will include treatment of microbial keratitis by antibiotic with sodium chloride 5% , the second group will include treatment by antibiotic only

Interventions

DRUGSodium chloride 5% solution

Use Sodium chloride 5% solution with usual anti microbial drugs

DRUGquinolones

Use of usual topical anti microbial treatment only

Sponsors

Sohag University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

IncluInclusion Criteria * Age ≥ 18 years. * Clinically diagnosed bacterial infectious keratitis * Positive corneal scraping or strong clinical suspicion of bacterial cause. * Ability to provide informed consent and attend follow-up visits

Exclusion criteria

* • Fungal, viral, or acanthamoeba keratitis. * Recent (\<7 days) topical corticosteroid use. * Corneal perforation or impending perforation. * History of hypersensitivity to study agents. * Systemic immunocompromised state (uncontrolled diabetes, Human immune defecinicy virus). * Poor compliance expected with follow-up.

Design outcomes

Primary

MeasureTime frameDescription
Control of infection6 monthsImprovement of manifestation according to rate of healing

Contacts

CONTACTNancy Safwat Kaldas, Specialist
nansy_safwat_post@med.sohag.edu.eg01200933440
CONTACTAmr Mounir Mohamed, Assistant professor
01005026170

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 6, 2026