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Angle-closure glaucoma registration study

The observational cohort study of acute primary angle closure and primary angle closure glaucoma

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800020216
Enrollment
Unknown
Registered
2018-12-20
Start date
2018-12-19
Completion date
Unknown
Last updated
2019-01-14

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

Conditions

Glaucoma

Interventions

Case series:Different treatment methods

Sponsors

The Eye Hospital, School of Ophthalmology and Optometry, Wenzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Aged 18 or above; 2. Acute primary angle closure patients diagnosed by glaucoma specialties: (1) presence of at least 180 degree of the posterior pigmented trabecular meshwork not visible on gonioscopy in the primary position of gaze without indentation in the affected eye; (2) raised IOP of at least 21 mmHg; (3) presence of at least 2 of the following symptoms: acute blurred vision, ocular pain, headache, nausea and vomitting; (3) presence of at lest 3 of the following signs: conjunctival injection, corneal epithelial edema, mid-dilated unreacitve pupil and/or a shallow anterior chamber; 3. Primary angle-closure glaucoma diagnosed by glaucoma specialties: (1) presence of at least 180 degree of the posterior pigmented trabecular meshwork not visible on gonioscopy in the primary position of gaze without indentation; (2) existence of glaucomatous optic neuropathy defined as neuroretinal rim loss with a vertical cup-to-disc ratio of greater than 0.7 or between eye vertical cup-to-disc ratio asymmetry of greater than 0.2; (3) a VF defect suggestive of glaucoma: the glaucoma hemifield test graded outside normal limits; a cluster of three contiguous points at the 5% level on the pattern deviation plot; Pattern standard deviation<0.05 in healthy poputlation. 4. informed consent obtained from the patient or their agent.

Exclusion criteria

Exclusion criteria: Patients with any of the following conditions: 1. ocular conditions effecting the intraocular pressure test; 2. corrected visual acuity worse than 0.5 logMAR, or other conditions reulting in disability to perform reliable visual field tests (reliable visual field tests defined as fixation losses < 20%, false-positive and false-negative rates of less than 15%) or OCT results (signal strength=6); 3. other cular conditions resulting in change of fundus and visual field results.

Design outcomes

Primary

MeasureTime frame
Best corrected visual acuity;intraocular pressure;visual field index;vertical cup to disc ration;central anterior chamber depth;

Secondary

MeasureTime frame
mean deviation;

Contacts

Public ContactLiang Yuanbo

The Eye Hospital, School of Ophthalmology and Optometry, Wenzhou Medical University

yuanboliang@126.com+86 18257748686

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026