An observational study in Endophthalmitis, sponsored by Assiut University. Not yet recruiting. Per ClinicalTrials.gov, last updated 2024-11-05.
Sponsored by Assiut University · Observational
65 studies on the registry are indexed under Endophthalmitis; 9 are open to participants now.
This study's planned enrollment of 41 is below the median of 100 across 20 observational studies indexed under Endophthalmitis.
Browse Endophthalmitis studies →Assiut University is the lead sponsor of 5,078 studies on the registry; 2,178 are open to participants now.
Of its 14 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.
Counted across the registry records on this site, refreshed daily.
Evaluation and risk factors of post-traumatic endophthalmitis with general and optical examination on patients exposed to eye trauma and developed post-traumatic endophthalmitis
Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.
Exclusion Criteria:
Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Informed consent
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
1. conception 2. acquisition of data 3. analysis of data
Diagnostic Test: ophthalmic saline eye drops · Drug: Saline
for optical examination
Most one natural and not effects on study
Knowledge of clinical features outcomes of post-traumatic endophthalmitis
Knowledge of clinical features which will be shown due to post-traumatic endophthalmitis
Time frame: Baseline
The factors associated with a worse prognosis in post-traumatic endophthalmitis
Discrimination the worst prognosis in post-traumatic endophthalmitis
Time frame: Baseline
No study locations are listed for this record.
This study is not yet recruiting, as verified in Oct 2024. You cannot join it, but the record below documents what was studied.
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Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.