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Monitoring the inflammatory process in active herpetic keratitis by in vivo confocal microscopy (IVCM): Clinical relevance.

Monitoring the inflammatory process in active herpetic keratitis by in vivo confocal microscopy: Clinical relevance.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON27960
Enrollment
120
Registered
2010-12-06
Start date
2011-04-01
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

Herpetic keratitis

Interventions

The diagnostic method used in this study to adjust medication will depend on the study-arm. Diagnostic outcome (active versus inactive HSK) will determine whether treatment is (re)started or stepped u

Sponsors

Het Oogziekenhuis Rotterdam (OZR) Postbus 70030 3000-LM Rotterdam
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Age ¡Ý 18 years; 2. Informed consent; 3. Unilateral disease; 4. Immune stromal keratitis in herpetic infection involving the optical axis; 5. Capable to cooperate (sitting still, fixing test light); 6. Group 1 and 2: At least 6 months after a clinical overt recurrence; 7. Group 3 and 4: At presentation with recurrence.

Exclusion criteria

Exclusion criteria: 1. Patients with proven ACV resistant strains; 2. Severe necrotizing herpetic keratitis; 3. Severe herpes related macula in the optical axis preventing visualisation of endothelium; 4. Herpetic stromal infection exclusively located in the peripheral 2 mm of the cornea; 5. Pre-existing ocular disease requiring surgical intervention within 12 months; 6. Pre-existing uncontrolled steroid glaucoma.

Design outcomes

Primary

MeasureTime frame
BCVA at 12 and 24 months follow up. Number of recurrences recognized in an earlier state by IVCM compared to slit lamp examination.

Secondary

MeasureTime frame
1. Side effects of treatment; 2. Amount of steroids used during 24 months follow up; 3. Dose of antiviral treatment used during 24 months follow up.

Contacts

Public ContactL. Remeijer

PO Box 70030

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)