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Completed

NCT Number: NCT01211327

Topical Cyclosporine for Vernal Keratoconjunctivitis (VKC) in Rwanda

Vernal keratoconjunctivitis (VKC) is a bilateral, chronic, external ocular inflammatory disease of unknown cause. It is a fairly common disease in hot, dry environments, representing as much as 3% of severe ophthalmic diseases and up to 33% of all eye pathology seen among young patients in eye clinics in Central Africa. Symptoms and signs can persist for years with an important visual morbidity and social impact. Corneal changes (e.g. corneal ulcers) can be sight threatening, occurring in up to 10% of VKC children. Topical steroid therapy remains the current standard treatment, but in developing countries its use often is chronic and not medically supervised, potentially leading to bacterial infections, steroid-induced glaucoma and cataract. Chromoglycate drops have less side effects but lack the power to control a flare-up. Topical cyclosporine has the potential to offer an efficient but safer alternative to steroid drops in the management of VKC in an African setting. Its safety and efficiency in the management of vernal keratoconjunctivitis have been described in several uncontrolled studies and double-blind, placebo-controlled trials, but those studies were relatively small and involved populations outside Africa with predominantly palpebral and mixed forms of VKC. Controversy still remains on the efficiency of cyclosporine in severe forms of allergic conjunctivitis like VKC. We therefore undertake a larger prospective randomized double-masked, standard treatment controlled clinical trial in Central Africa to compare the short-term efficiency of cyclosporine A (CsA) 2% eye drops, solved in olive oil vehicle, with that of steroid drops in predominantly limbal forms of VKC. During 4 weeks the participants will be randomised to either cyclosporine or dexamethasone as attack treatment for VKC. The 4 weeks thereafter all participants will receive chromoglycate drops as maintenance treatment. Additional objectives are to document any difference in rebound phenomenon while on chromoglycate during the maintenance phase between the 2 treatment groups and to evaluate safety and tolerance of the test medication.

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Key information

Age range

5 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Kabgayi Hospital

Gitarama/Muhanga, Rwanda

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • at least 5 years of age

Exclusion criteria

  • being pregnant
  • suffering from any other infectious or inflammatory ocular pathology
  • using topical/ systemic corticosteroids, antihistamines, non-steroidal anti-inflammatory drugs or immunosuppressives 2 weeks prior to the trial
  • been treated with steroid injection 6 months prior to the study

Treatment and study plan

Cyclosporine A

Drug

Cyclosporine 2% eye drops

Dexamethasone

Drug

Dexamethasone 0,1% eye drops

Primary outcomes

  1. Difference in score for symptoms and clinical signs between treatment arms

    Time frame: After 4 weeks at the end of 4 weeks test medication

    Differences in scores for symptoms and clinical signs individually and as a composite score between the treatment arms.

    Symptoms are itchiness, tearing, stinging, discharge and photophobia. Signs are subtarsal scarring, limbal cysts, pseudogerontoxon, pseudomembrane, corneal plaque, shield-ulcer, bulbar hyperaemia, limbal pigmentation, punctate keratitis, tarsal plate papillae, corneal astigmatism, limbal follicles, conjunctivalisation of the cornea and trantas dots.

Secondary outcomes

  1. Speed of symptom/sign reduction

    Time frame: At 2 weeks while on test medication and at 8 weeks at the end of a chromoglycate maintenance phase

    To document any difference between the 2 treatment groups in speed of symptom/sign reduction during the attack treatment and in rebound phenomenon while on chromoglycate during the maintenance phase

  2. Safety and tolerance of the test medication

    Time frame: At 2 weeks while on test medication and at 8 weeks at the end of a chromoglycate maintenance phase

    To evaluate safety and tolerance of the test medication.

Sponsors and collaborators

Lead sponsor

University Hospital, Ghent

Other

Collaborators

  • Funds for Research in Ophthalmology (FRO) of Belgium
  • Novartis

Registry information

Official study title

Topical Cyclosporine in the Treatment of Vernal Keratoconjunctivitis in a Rwandan Eye Clinic; a Prospective Randomized Double-masked Clinical Trial

Important dates

Study start
2008
Primary completion
2008
Study completion
2008
First posted
Sep 29, 2010
Registry last updated
Sep 29, 2010

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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