Menu
Recruiting NCT07539675

The Multi-Omics Analysis of Lens Zonule Relaxation in The PACG Pathogenesis

Observational Primary Angle-Closure Glaucoma

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: No Additional Experimental Intervention.
Who it may be relevant to
Registry conditions: Primary Angle-Closure Glaucoma. Basic parameters: from 50 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
China
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

Compared with primary angle-closure glaucoma (PACG) patients without zonular laxity and the control group, there are differentially expressed molecules in PACG patients with zonular laxity, and a potential mechanistic network can be constructed therefrom.

Detailed description

This study investigates the pathogenesis of PACG by conducting multi-omics analyses of aqueous humor, blood and anterior lens capsule samples from PACG patients with and without concomitant zonular abnormalities, aiming to elucidate the etiology of zonular abnormalities and uncover novel mechanisms underlying their involvement in the pathogenesis of glaucoma.

Interventions

  • Other No Additional Experimental Intervention
    No Additional Experimental Intervention

Primary outcome measures

  • Concentration of differentially expressed molecules in PACG patients with zonular laxity [Time frame: 2 years]

Eligibility criteria

Inclusion criteria

  • Clinically diagnosed with primary angle-closure glaucoma (PACG)
  • Aged ≥ 50 years, no gender restriction
  • Case Group A: Undergoing glaucoma surgery with intraoperatively confirmed significant zonular laxity
  • Case Group B: Undergoing glaucoma surgery with intraoperatively confirmed normal zonular morphology
  • Control group: age- and sex-matched with case groups; clinically diagnosed with age-related cataract; normal anterior chamber depth and angle; no history or signs of glaucoma; undergoing cataract surgery

Exclusion criteria

  • Secondary glaucoma
  • History of previous intraocular surgery
  • Systemic diseases that can cause abnormal ocular zonules
  • Other severe ocular diseases
  • Long-term use of medications affecting connective tissue metabolism

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Case-control

Study locations

China · 1 center
  • Zhongnan Hospital of Wuhan University — Wuhan

Identifiers

NCT: NCT07539675 · 20260122xrd

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗