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A comparative study of clinical outcomes using Kahook dual blade and gonioscopy-assisted transluminal trabeculotomy for juvenile open angle glaucoma

A comparative study of clinical outcomes using Kahook dual blade and gonioscopy-assisted transluminal trabeculotomy for juvenile open angle glaucoma

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000034172
Enrollment
Unknown
Registered
2020-06-27
Start date
2020-07-01
Completion date
Unknown
Last updated
2020-06-29

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

Conditions

Juvenile open angle glaucoma

Interventions

Left eye group :Kahook dual blade
Right eye group:Gonioscopy assisted transluminal trabeculotomy

Sponsors

Fudan University Affiliated Ophthalmotolaryngology Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
10 Years to 40 Years

Inclusion criteria

Inclusion criteria: 1. Patients with both eyes meeting the JOAG diagnosis and requiring surgery; 2. Age: 10-40 years old, gender: unlimited; 3. The patients with open angle and the structure of angle accord with the characteristics of angle dysplasia; 4. The patients whose IOP was more than or equal to 21mmhg under the treatment of the most tolerable IOP lowering drugs; 5. Patients with glaucomatous optic neuropathy in both eyes; 6. Patients and their families volunteered to participate in the study, signed informed consent and agreed to follow-up according to the study plan.

Exclusion criteria

Exclusion criteria: 1. Any patient whose eyesight is no light sense; 2. Patients with clinical characteristics of congenital glaucoma (corneal enlargement, Haab lines, etc.); 3. Patients with secondary factors of ocular or systemic hypertension; 4. Patients who have undergone any internal eye surgery or anti glaucoma surgery before; 5. Patients who have previously received any intraocular laser treatment (such as laser peripheral iridotomy, retinal photocoagulation, etc.), but excluding selective laser trabeculoplasty; 6. Patients who have participated in any other clinical study.

Design outcomes

Primary

MeasureTime frame
applanation tonometry;number and types of medicaitons;

Secondary

MeasureTime frame
best corrected visual acuity;visual field;

Countries

China

Contacts

Public ContactJunyi Chen

Fudan University Affiliated Ophthalmotolaryngology Hospital

chenjy@fudan.edu.cn+86 18917785539

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 20, 2026