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: 2025-12-25 @ 12:43 AM
Ignite Modification Date: 2025-12-25 @ 12:43 AM
NCT ID: NCT00800267
Eligibility Criteria: Inclusion Criteria: * Unilateral or bilateral primary open angle glaucoma, capsular glaucoma, pigmentary glaucoma or ocular hypertension. * Patients currently on IOP reducing therapy: IOP greater than or equal to 25mmHg (Ltwo IOP determinations at pre-study separated by at least one hour) OR Patients without IOP reducing therapy: IOP greater than or equal to 30mmHg (two IOP determinations at pre-study separated by at least one hour). Exclusion Criteria: * History of acute angle closure or closed/barely open anterior chamber angle. * Current use of contact lenses. * Ocular surgery or argon laser trabeculoplasty (ALT) within three months prior to pre-study visit. * Ocular inflammation/infection occurring within three months prior to pre-study visit. * Hypersensitivity to benzalkonium chloride or to any other component of the study drug solutions. * Other abnormal ocular condition or symptom preventing the patient from entering the study, according to the investigator's judgement. * Patients with conditions in which treatment with B-blocking agents are contraindicated: cardiac failure, sinus bradycardia, second and third degree atrio-ventricular block. * Patients with conditions in which treatment with B-blocking agents are contraindicated: bronchial asthma, history of bronchial asthma or chronic obstructive pulmonary disease. * Inability to adhere to treatment/visit plan. * Have participated in any other clinical study within one month prior to pre-study visit.
Healthy Volunteers: False
Sex: ALL
Minimum Age: 18 Years
Study: NCT00800267
Study Brief:
Protocol Section: NCT00800267