Skip to content

The safety andefficacy of collagen matrix (trade name: Ologen) in the treatment of glaucoma

The safety andefficacy of collagen matrix (trade name:Ologen) in the treatment of glaucoma

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IPR-15007121
Enrollment
Unknown
Registered
2015-09-18
Start date
2015-09-23
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

glaucoma

Interventions

experimental group/control group:subconjunctival Ologen implantation

Sponsors

West China Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
35 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) age 35 to 75; (2) phakic eyes with primary glaucoma which are in maximal tolerated medical therapy andIOP?18 mmHg,has been confirmed twice before inclusion; (3) best corrected visual acuity no less than 20/80; (4) subjects must sign informed consent; (5) subjects willing to cooperate to complete the follow-up after surgery.

Exclusion criteria

Exclusion criteria: (1) discernable congenital anomaly; (2) secondary glaucoma; (3) other disease which may effect IOP of subject eyes; (4) subjects who have undergone hematodialysis or peritoneal dialysis; (5) laser retinal treatment anterior to thevortex vein ampullae or retinal cryotherapy(retinal holes anterior to thevortex vein ampullae refer to less than two quadrants),laser treatment or surgery on subject eyes; (6) proliferative or non-proliferative retinopathy; (7) expanded pupil diameter less than 2mm; (8) field loss attribute to other conditions except for glaucoma; (9) field deep sclerectomy procedures on subject eyes.for example: leakage of eye balls because of excessive drainage or barely no drainage because of not enough depth in sclerectomy; (10) patients who may need MMC in trabeculectomy; (11) allergic to porcine -derived collagen; (12) pregnant or plan to become pregnant or in lactation period.

Design outcomes

Primary

MeasureTime frame
intraocular pressure;best corrected visual acuity;success rate of surgery;morphology of blebs;compliactions;visual fields;

Countries

China

Contacts

Public ContactTang Li
tangli-1a@163.com+86 18980601748

Outcome results

None listed

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