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NCT05123014

Lenticule Implantation and Autologous Serum New Approach in Treatment of Adenoviral Keratitis Disease

Active, enrolled NA Last updated 25 February 2025
What this trial tests

NA trial testing relex smile in Adenoviral Keratoconjunctivitis in 45 participants. Participants enrolled and being followed up; not accepting new ones.

Timeline
1 February 2018
Primary endpoint
1 February 2019
1 February 2027

Quick facts

Lead sponsorEye Hospital Pristina Kosovo
PhaseNA
StatusActive, enrolled
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment45
Start date1 February 2018
Primary completion1 February 2019
Estimated completion1 February 2027
Sites1 location across Kosovo

Drugs / interventions tested

Conditions studied

Sponsor

Eye Hospital Pristina Kosovo

Who can join

Adults 24 to 43, any sex, with Adenoviral Keratoconjunctivitis. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Adenoviral keratitis(caused by adenovirus) is one of the most frequently diagnosed eye diseases. Most of these infections have symptoms like (Ocular itchiness and irritation, chemosis (conjunctival edema),photophobia, epiphora, foreign body sensation, epithelial keratitis etc.Adenoviral subepithelial infiltration is one of the most difficult complication to treat. Our purpose is to evaluate corneal transparency, recurrence, and visual acuity in patients with adenoviral subepithelial infiltration by first removing the infiltrative stroma with a smile and implanting the same volume of fresh lenticule in the prepared stromal pocket.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other Eye Hospital Pristina Kosovo trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05123014.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing