NCT06673784

Brief Summary

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

Trial Health

35
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
41

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Nov 2024

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

October 31, 2024

Completed
5 days until next milestone

First Posted

Study publicly available on registry

November 5, 2024

Completed
5 days until next milestone

Study Start

First participant enrolled

November 10, 2024

Completed
1.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 28, 2026

Completed
1 day until next milestone

Study Completion

Last participant's last visit for all outcomes

March 1, 2026

Completed
Last Updated

November 5, 2024

Status Verified

October 1, 2024

Enrollment Period

1.3 years

First QC Date

October 31, 2024

Last Update Submit

November 2, 2024

Conditions

Endophthalmitis

Outcome Measures

Primary Outcomes (1)

  • Knowledge of clinical features outcomes of post-traumatic endophthalmitis

    Knowledge of clinical features which will be shown due to post-traumatic endophthalmitis

    Baseline

Secondary Outcomes (1)

  • The factors associated with a worse prognosis in post-traumatic endophthalmitis

    Baseline

Study Arms (1)

Evaluation of post-traumatic endophthalmitis

1. conception 2. acquisition of data 3. analysis of data

Diagnostic Test: ophthalmic saline eye dropsDrug: Saline

Interventions

ophthalmic saline eye dropsDIAGNOSTIC_TEST

for optical examination

Evaluation of post-traumatic endophthalmitis
SalineDRUG

Most one natural and not effects on study

Evaluation of post-traumatic endophthalmitis

Eligibility Criteria

Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Evaluation and risk factors of post-traumatic endophthalmitis with general and optical examination on patients exposed to eye trauma and developed post-traumatic endophthalmitis

You may qualify if:

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

You may not qualify if:

  • Patients who refuse to sign informed consent in this study

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Related Publications (1)

  • Alfaro DV, Roth DB, Laughlin RM, Goyal M, Liggett PE. Paediatric post-traumatic endophthalmitis. Br J Ophthalmol. 1995 Oct;79(10):888-91. doi: 10.1136/bjo.79.10.888.

    PMID: 7488575BACKGROUND

MeSH Terms

Conditions

Endophthalmitis

Interventions

Sodium Chloride

Condition Hierarchy (Ancestors)

Eye InfectionsInfectionsEye Diseases

Intervention Hierarchy (Ancestors)

ChloridesHydrochloric AcidChlorine CompoundsInorganic ChemicalsSodium Compounds

Central Study Contacts

Hadeer Gamal AbdElmohsen, 3

CONTACT

00201091593658hadeergamal294@gmail.com

Mohamed Sayed Saad, 1

CONTACT

00201001825024mohsayedsaad@aun.edu.eg

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Doctor

Study Record Dates

First Submitted

October 31, 2024

First Posted

November 5, 2024

Study Start

November 10, 2024

Primary Completion

February 28, 2026

Study Completion

March 1, 2026

Last Updated

November 5, 2024

Record last verified: 2024-10