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A comparative study on the clinical efficacy of minimally invasive glaucoma surgery and traditional trabeculectomy

A comparative study on the clinical efficacy of minimally invasive glaucoma surgery and traditional trabeculectomy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500108196
Enrollment
Unknown
Registered
2025-08-26
Start date
2025-10-10
Completion date
Unknown
Last updated
2025-09-01

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

Conditions

Glaucoma

Interventions

Traditional glaucoma surgery group:Trabeculectomy will performed.
Group A of Minimally Invasive Glaucoma Surgery:Implantation of XEN gel scaffold drainage tube.
Group B of Minimally Invasive Glaucoma Surgery:Ultrasound ciliary plasty will be performed.

Sponsors

Xiamen Eye Center Affiliated to Xiamen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Patients diagnosed with glaucoma (including primary open-angle glaucoma, angle-closure glaucoma, secondary glaucoma, etc.) who meet the indications for surgical treatment. 2.No restrictions on age or gender, and able to cooperate with preoperative examinations, surgery, and medium-to-long-term postoperative follow-up. 3.Voluntarily participate in the study and sign the informed consent form. 4.Complete clinical data, including baseline data such as preoperative intraocular pressure, visual acuity, and visual field, as well as results of relevant ocular examinations.

Exclusion criteria

Exclusion criteria: 1.Patients with severe ocular infections, acute ocular trauma, or other severe ocular diseases that may affect surgical efficacy or follow-up evaluation. 2.Patients with uncontrolled severe systemic diseases (e.g., uncontrolled hypertension, diabetes, cardiovascular and cerebrovascular diseases) who cannot tolerate surgery or follow-up. 3.Patients who have undergone other previous glaucoma surgeries that may interfere with the efficacy evaluation of this study. 4.Patients with mental disorders, cognitive dysfunction, or other conditions that prevent cooperation with examinations and follow-up. 5.Patients allergic to materials used in surgery. 6.Patients with incomplete clinical data that cannot meet the requirements for research data collection.

Design outcomes

Primary

MeasureTime frame
intraocular pressure;best-corrected visual acuity;ocular surface disease index;Numerical Rating Scale (NRS);

Countries

China

Contacts

Public ContactBin Lin

Xiamen Eye Center Affiliated to Xiamen University,

linbin1513@foxmail.com+86 180 3985 0146

Outcome results

None listed

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