Evaluation and Risk Factors of Post-traumatic Endophthalmitis

Status

Not yet recruiting

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT06673784

Enrollment

Registered

2024-11-05

Start date

2024-11-10

Completion date

2026-03-31

Last updated

2024-11-05

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

Conditions

Endophthalmitis

Brief summary

1. identify the incidence of post-traumatic endophthalmitis and the related risk factors influencing its development. 2. study the clinical- microbiological profile and evaluate the functional and anatomical outcomes of post-traumatic endophthalmitis (PPTE).

Interventions

DIAGNOSTIC_TESTophthalmic saline eye drops

for optical examination

DRUGSaline

Most one natural and not effects on study

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Healthy volunteers

Inclusion criteria

* Patients exposed to eye trauma and developed post-traumatic endophthalmitis

Exclusion criteria

* Patients who refuse to sign informed consent in this study

Design outcomes

Primary

Measure	Time frame	Description
Knowledge of clinical features outcomes of post-traumatic endophthalmitis	Baseline	Knowledge of clinical features which will be shown due to post-traumatic endophthalmitis

Secondary

Measure	Time frame	Description
The factors associated with a worse prognosis in post-traumatic endophthalmitis	Baseline	Discrimination the worst prognosis in post-traumatic endophthalmitis

Contacts

Primary ContactHadeer Gamal AbdElmohsen, 3

hadeergamal294@gmail.com00201091593658

Backup ContactMohamed Sayed Saad, 1

mohsayedsaad@aun.edu.eg00201001825024

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026