Trial | NCT00449098  Report issue

Title

Ologen (OculusGen)-Glaucoma MMC Control Trial in India
Comparative Study of the Safety and Effectiveness Between Ologen (OculusGen) Collagen Matrix Implant and Mitomycin-C in Glaucoma Filtering Surgery

  • Phase

    Phase 4

  • Study Type

    Interventional

  • Status

    Unknown status

  • Intervention/Treatment

    collagen ...

  • Study Participants

    40
The purpose of this study is to compare the safety and effectiveness of the ologen (OculusGen) Biodegradable Collagen Matrix Implant and the MMC group in filtration surgery.
Study Objective: To compare the safety and effectiveness of the ologen (OculusGen) Biodegradable Collagen Matrix Implant and the MMC group in filtration surgery. The primary endpoint is to prove the effectiveness via the reduction of IOP, and the secondary endpoint is to prove the safety via the incidence of complications and adverse events.
Study Design: The study is designed as an open-label, randomized, parallel, comparative study. Patients who meet the inclusion/exclusion criteria and sign informed consent will be included. After enrollment, patients will be randomized into two groups: trabeculectomy with ologen (OculusGen) implant or trabeculectomy with mitomycin-C.
Follow-Up: There will be 7 post-operative and follow-up visits within 6 months of surgery: postoperative days 1, 7, 14, 30, 60, 90 and 180. A window of ± 7 days is allowed for the 30, 60, 90 day visits and ± 14 days for the 180 day visits. Further follow-up of subjects after the trial will be the responsibility of the investigator.
Study Started
Jan 31
2007
Primary Completion
Oct 31
2011
Anticipated
Study Completion
Oct 31
2011
Anticipated
Last Update
Oct 07
2011
Estimate

Device OculusGen Biodegradable Collagen Matrix Implant

Trabeculectomy with OculusGen Biodegradable Collagen Matrix Implant

Drug Trabeculectomy with MMC

Trabeculectomy with MMC

OculusGen Biodegradable Collagen Matrix Implant Experimental

Trabeculectomy with OculusGen Biodegradable Collagen Matrix Implant

MMC Active Comparator

Trabeculectomy with MMC

Criteria 

Inclusion Criteria:

Age 18 years or over.
Uncontrolled glaucoma, with failed medical and laser treatment, requiring trabeculectomy.
Subject able and willing to cooperate with investigation plan.
Subject able and willing to complete postoperative follow-up requirements.
Subject willing to sign informed consent form.

Exclusion Criteria:

Known allergic reaction to mitomycin-C or porcine collagen.
Subject is on warfarin and discontinuation is not recommended.
Normal tension glaucoma.
Participation in an investigational study during the 30 days preceding trabeculectomy.
Ocular infection within 14 days prior to trabeculectomy.
Pregnant or breast-feeding women.
No Results Posted