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Completed

NCT Number: NCT00661583

Use of Ranibizumab With Mitomycin C During Trabeculectomy

The purpose of the study is to study the safety of the combination of ranibizumab and MMC vs monotherapy MMC vs intravitreal ranibizumab injection in patients with glaucoma.

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Key information

Age range

21 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1 / Phase 2

Primary location

Rocky Mountain Lions Eye Institute

Aurora, Colorado, 80045, United States

About this study

A common problem after undergoing trabeculectomy surgery to create a bleb (blister or bubble) to reduce intraocular pressure, is scarring of the opening. This scarring prevents fluid drainage and interferes with the proper functioning of the bleb. MMC (Mitomycin C) is usually administered intraoperatively, to reduce scarring and increase filtration. However, the failure rate of trabeculectomy remains high. Anti-VEGF (Vascular endothelial growth factor) agents have been used successfully in cases requiring bleb needling. The purpose of the study is to determine the safety of the combination of ranibizumab and MMC vs monotherapy MMC in patients with glaucoma.

This is an open-label, Phase I/II safety study of 30 patients randomized to either treatment with ranibizumab 0.5 mg intravitreally injected (n=10), combination ranibizumab 0.5mg intravitreally injected and MMC (0.4 mg/ml for 2 min) in eyes after trabeculectomy (n=10) or MMC therapy alone (n=10).

For the ranibizumab groups, a repeat injection of ranibizumab 0.5mg may be given PRN (as needed) at 1 month if hypervascularity or neovascularization of the conjunctiva exists.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • glaucoma
  • undergoing trabeculectomy
  • 21 years of age or older

Exclusion criteria

  • pregnancy or lactation
  • any condition the investigator believes would impose a significant hazard to the patient if investigational therapy were initiated
  • history of ocular surface disease
  • cataract surgery in the past 6 months
  • history of active inflammatory, infectious or idiopathic keratitis

Treatment and study plan

ranibizumab

Drug

0.5mg of ranibizumab intravitreally injected after surgery and at 1 month if needed

Ranibizumab and MMC

Drug

Combination ranibizumab 0.5mg intravitreally injected and MMC (0.4 mg/ml for 2 min) in eyes after trabeculectomy

Other names: Ranibizumab and Mitomycin C

MMC

Drug

MMC (0.4 mg/ml for 2 min) in eyes after trabeculectomy.

Other names: Mitomycin C

Primary outcomes

  1. Assessment of Ocular Adverse Events

    Time frame: 6 months

    To assess ocular adverse events of combination ranibizumab and MMC therapy at 6 months

Secondary outcomes

  1. Percent of Subjects With a Qualified Success and Viable Bleb at 6 Months.

    Time frame: 6 months

    To determine percent of subjects with a qualified success and viable bleb at 6 months (IOP between 6mm Hg and 22 mm Hg with pressure controlled with and without adjunctive medications)

  2. Mean Change in in Intraocular Pressure.

    Time frame: 6 months

    Mean change in in intraocular pressure at 3 months and at 6 months

  3. Mean Change in Visual Acuity

    Time frame: 6 months

    Mean change in visual acuity in logMAR.

Sponsors and collaborators

Lead sponsor

University of Colorado, Denver

Other

Collaborators

  • Genentech, Inc.

Registry information

Official study title

Occlusion Prevention for Trabeculectomy Procedures Using Combination Ranibizumab and Mitomycin C (MMC) During Surgery (OCTOPUS Study)

Acronym: OCTOPUS

Important dates

Study start
2008
Primary completion
2014
Study completion
2014
First posted
Apr 18, 2008
Registry last updated
Oct 13, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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