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A Study on Intraocular Pressure Fluctuation Patterns and Clinical Management in Chinese Glaucoma Patients Based on Home IOP Monitoring and Association with Special Events (CHGIS Study)

A Study on Intraocular Pressure Fluctuation Patterns and Clinical Management in Chinese Glaucoma Patients Based on Home IOP Monitoring and Association with Special Events

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600118859
Enrollment
Unknown
Registered
2026-02-11
Start date
2026-02-23
Completion date
Unknown
Last updated
2026-02-16

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

Conditions

Glaucoma

Interventions

Observation group:None

Sponsors

Eye &ENT Hospital of Fundan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Meet the diagnostic criteria in China Glaucoma Guidelines (2020) (for POAG: intraocular pressure >=21mmHg; for NTG: accompanied by optic disc/visual field abnormalities; for angle-closure glaucoma: angle closure >=180°); 2. Understand the importance and necessity of home intraocular pressure measurement, and receive training on the rebound-type home tonometer; 3. Be able to independently provide at least 1 visual field examination and 1 fundus image collection per year; 4. Aged >=18 years, gender not limited; 5. Have basic smartphone operation skills, and be proficient in using the rebound tonometer mini-program for data entry and monitoring; 6. Voluntarily participate in this study and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1.Corneal thickness measurement error > 5µm; 2.Optic disc area obstruction in fundus images > 10% (e.g., cataracts, vitreous opacity); 3.Patients with contraindications to the use of rebound tonometers (e.g., active ocular infection, nystagmus, etc.); 4.Complicated with severe cardiac, hepatic, renal or other organ dysfunction, unable to complete 2-year follow-up; 5.Patients with mental illness or cognitive impairment, unable to cooperate with monitoring and data recording; 6.Simultaneously participating in other similar glaucoma-related clinical studies.

Design outcomes

Primary

MeasureTime frame
Intraocular pressure fluctuation parameters: including 24-hour IOP peak, trough, standard deviation, amplitude, and weekly-scale IOP peak, trough, standard deviation, amplitude.;Intraocular pressure;

Secondary

MeasureTime frame
The correlation strength between special events and intraocular pressure fluctuations: Calculate the intraocular pressure change values and HR values after the occurrence of various events;The fluctuation control effects of different treatment regimens: Comparing the HR values for controlling intraocular pressure fluctuations among drug, surgical, and laser treatment regimens;Corneal thickness;Examination of visual field;Fundus image acquisition;Diagnosis of glaucoma types;Screening for concurrent chronic diseases (hypertension/diabetes);

Countries

China

Contacts

Public ContactSun Xinghuai

Eye and ENT Hospital Affiliated to Fudan University

xhsun@shmu.edu.cn+86 139 1661 8678

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 19, 2026