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Study on the factors influencing the efficacy of micropulse transscleral laser treatment in glaucoma and its related mechanisms

Study on the factors influencing the efficacy of micropulse transscleral laser treatment in glaucoma

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400079937
Enrollment
Unknown
Registered
2024-01-16
Start date
2024-02-01
Completion date
Unknown
Last updated
2024-01-22

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

Conditions

glaucoma

Interventions

Retrospective study of patients:none
Prospective study of patients:none

Sponsors

Changsha Aier Eye Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Patients in prospective studies: a. The patient voluntarily participates in this study, signs the informed consent form, and agrees to be followed up in accordance with the research plan; b. Glaucoma patients undergoing mTLT include but are not limited to primary open-angle glaucoma, primary angle-closure glaucoma, secondary glaucoma, neovascular glaucoma, intraocular pressure failure to decrease after anti-glaucoma surgery, etc. (2) Patients in retrospective study: a. Patients who received mTLT treatment in our hospital since September 2022 but were not included in prospective follow-up, including but not limited to primary open-angle glaucoma, primary angle-closure glaucoma, secondary glaucoma, neovascular glaucoma, and anti-glaucoma Intraocular pressure does not decrease after surgery.

Exclusion criteria

Exclusion criteria: Prospective study: a. Combined with active eye inflammation, such as acute conjunctivitis, acute uveitis, etc.; b. Combined with a history of serious systemic diseases: diabetes, hypertension (systolic blood pressure = 160mmHg or diastolic blood pressure = 100mmHg), heart disease, kidney disease, rheumatic immunity, digestive system diseases, tumors, etc.; c. Pregnant or lactating women, and patients younger than 18 years old. Retrospective study: patients whose postoperative review time in our hospital was less than 1 month.

Design outcomes

Primary

MeasureTime frame
intraocular pressure;

Secondary

MeasureTime frame
Postoperative complications;The number of intraocular pressure lowering drugs used;

Countries

China

Contacts

Public ContactXuanchu Duan

Changsha Aier Eye Hospital

duanxchu@csu.edu.cn+86 138 0731 4691

Outcome results

None listed

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