Condition: Eye Disease · Conjunctivitis · Sponsor: Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Data will be gathered from patients who report having any kind of recurrent conjunctivitis and who, in accordance with clinical practice, are scheduled to have intravitreal injections, glaucoma surgery, cataract surgery, vitrectomy, combined cataract and vitrectomy, or corneal transplantation. The data will be obtained using pseudonyms from the patients' medical records and will include the outcomes of swabs and surgeries performed in accordance with clinical practice for the patient's condition. The following swabs will be taken into consideration for data analysis: Four days before to surgery, a conjunctival swab is used to check for the presence and load of species that do not make up the typical conjunctival flora (Baseline-T0). On the day of operation, a conjunctival swab is taken before to entering the recovery room (T1). Following three minutes of 5% iodopovidone instillation in the eye to be operated on, a conjunctival swab (T2) was used. Additionally, we will gather follow-up data from the medical record 24 and 30 hours after surgery (at day 34 +/- 7 days).
This description comes directly from the study's public registry record.
Stanislao Rizzo, MD, Prof · 0630151 · oculistica@policlinicogemelli.it
Valentina Cestrone, Dr · 0630154528 · valentina.cestrone@guest.policlinicogemelli.it
Always discuss trial participation with your own doctor first.
| Prof. Stanislao Rizzo | Rome, Italy | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06771908