Eligibility Module

Eligibility Module

The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.

Eligibility Module path is as follows:

Study -> Protocol Section -> Eligibility Module

Eligibility Module


Ignite Creation Date: 2025-12-24 @ 6:39 PM
Ignite Modification Date: 2025-12-24 @ 6:39 PM
NCT ID: NCT02943057
Eligibility Criteria: Inclusion Criteria: * Age between 21 and above * Patients who are diagnosed with anterior uveitis or endotheliitis with a positive aqueous real time PCR (RT-PCR) and/or positive tetraplex PCR for Cytomegalovirus (CMV) * Patients with relapses and recurrent anterior segment disease that is PCR positive for CMV in aqueous * Have not been on any form of (topical, local or systemic) ganciclovir therapy for the past 1 month * Consent to undergo anterior chamber tap and give aqueous and tear samples for the study * Able to undergo relevant tests (e.g. laser flare cell photometry) * Able to come for subsequent follow-up visits * Ability to provide informed consent Exclusion Criteria: * CMV anterior uveitis with associated retinitis * Other causes of hypertensive anterior uveitis / endotheliitis such as HSV, VZV infection * Patients who have been on any form of (topical, local or systemic) ganciclovir therapy for the past1 month. * Patients who are allergic to ganciclovir * Patients who will require systemic or intra-vitreal ganciclovir therapy * Immunocompromised patients * Positive for HIV, Hep B and Hep C * Not keen on participating in the study * Patients who are incapable, either by law or mental state, of giving consents in their own right. * Patients who are either unable or unwilling to keep scheduled appointments and adhere to the other aspects of the protocol * Patients who are pregnant or breastfeeding * Any other specified reason as determined by the clinical investigator.
Healthy Volunteers: False
Sex: ALL
Minimum Age: 21 Years
Study: NCT02943057
Study Brief:
Protocol Section: NCT02943057