search
Back to results

Subconjunctival Versus Direct Mitomycin C in Trabeculectomy

Primary Purpose

Open Angle Glaucoma

Status
Completed
Phase
Phase 4
Locations
Study Type
Interventional
Intervention
Mitomycin-C injection
Mitomycin-C sponge
Sponsored by
University of California, San Diego
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Open Angle Glaucoma focused on measuring trabeculectomy, mitomycin-C, glaucoma

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • medically uncontrolled glaucoma
  • healthy and freely mobile conjunctiva in superior bulbar region

Exclusion Criteria:

  • previous incisional glaucoma surgery
  • no light perception vision
  • pregnant or nursing women
  • iris neovascularization or proliferative retinopathy
  • iridocorneal endothelial syndrome
  • chronic or recurrent uveitis
  • steroid-induced glaucoma
  • pathologic myopia or refractive error less than -6.00 diopters
  • unwillingness or inability to give consent
  • inability to return for scheduled protocol visits

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Active Comparator

    Active Comparator

    Arm Label

    Injection group

    Sponge group

    Arm Description

    MMC delivered by preoperative subconjunctival injection

    MMC delivered by intraoperative direct scleral application with impregnated cellulose sponges

    Outcomes

    Primary Outcome Measures

    Percentage of Participants Achieving Intraocular Pressure Reduction Thresholds
    Percentage of patients achieving at least a 30% mean intraocular pressure reductions from baseline and with an intraocular pressure <21 mm Hg. Subjects that met this criteria without the use of intraocular pressure lowering medications were classified as "Complete Success." Subjects that met this criteria but required the use of intraocular pressure lowering medications were classified as "Qualified Success." Subjects that failed to meet this criteria were classified as "Failure." Subjects that failed to meet this criteria and required additional glaucoma surgery were classified as "Complete Failure."

    Secondary Outcome Measures

    Bleb Morphology
    Bleb morphology at 6 months was graded using Indiana Bleb Appearance Grading Scale. Bleb height was graded on a scale of 0 to 3 (0: flat bleb without visible elevation, 1: low bleb elevation, 2: moderate bleb elevation, 3: high bleb elevation). Bleb extent was graded on a scale of 0 to 3 (0: no visible bleb extent to less than 1 clock hour, 1: extent equal to or greater than 1 clock hour but less than 2 clock hours, 2: extent equal to or greater than 2 clock hours but less than 4 clock hours, 3: extent equal to or greater than 4 clock hours). Bleb vascularity was graded on a scale of 0 to 4 (0: avascular/white, 1: avascular/cystic, 2: mild vascularity, 3: moderate vascularity, 4: extensive vascularity). Scales are descriptive and do not necessarily represent better or worse outcomes.
    Medications
    Number of intraocular pressure lowering medications used by the patient at follow up visit.
    Visual Acuity
    Change in visual acuity from baseline
    Number of Participants With Surgical Complications
    Number of eyes that experienced surgical complications following surgery
    Number of Participants Requiring Additional Surgery
    Number of eyes requiring additional surgery from each group
    Postoperative Interventions
    Mean number of postoperative interventions (needling, antifibrotic injections) performed in each group

    Full Information

    First Posted
    April 15, 2020
    Last Updated
    June 14, 2020
    Sponsor
    University of California, San Diego
    search

    1. Study Identification

    Unique Protocol Identification Number
    NCT04352660
    Brief Title
    Subconjunctival Versus Direct Mitomycin C in Trabeculectomy
    Official Title
    Subconjunctival Versus Direct Scleral Application of Mitomycin-C in Trabeculectomy
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    June 2020
    Overall Recruitment Status
    Completed
    Study Start Date
    May 23, 2016 (Actual)
    Primary Completion Date
    April 14, 2019 (Actual)
    Study Completion Date
    April 14, 2019 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    University of California, San Diego

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    Yes
    Studies a U.S. FDA-regulated Device Product
    No
    Product Manufactured in and Exported from the U.S.
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    Trabeculectomy is routinely used as a surgical treatment for open angle glaucoma. Success of trabeculectomy is greatly augmented by the use of antimetabolites to inhibit wound healing, specifically Mitomycin C (MMC). MMC can be applied to the eye at various sites, concentrations and times. This study aims to compare the two application routes that are commonly employed: subconjunctival pre-operative injection and intraoperative direct scleral application in terms of IOP lowering effect, bleb appearance and complications.
    Detailed Description
    Trabeculectomy is widely used as a surgical treatment of uncontrolled open glaucoma. Success of trabeculectomy at halting or slowing glaucoma progression primarily relies on the extent of conjunctival and sclera wound healing. The success rates of trabeculectomy increased dramatically with the introduction of anti-metabolites. For more than two decades mitomycin-c (MMC), a chemotherapeutic agent capable of decreasing fibroblast activity and modulating wound healing at the bleb, has been used with trabeculectomy. The complications of MMC are well known and several studies have described various methods of application based on exposure time, dose and surface area. Numerous retrospective and prospective studies have compared the efficacy of MMC applied beneath the conjunctival flap with soaked sponges versus intrascleral application. In 2008, Lee et al. first described an alternative route of application: subconjunctival injection of MMC directly into the intra-Tenon area. Seventy-six eyes with primary and secondary open angle glaucoma underwent trabeculectomy with this approach and were followed for one year post-operatively. Eighty-six percent of eyes achieved an IOP <21 mm Hg and 57% an IOP<14 mm Hg at one year without adjunctive drops. Transient complications included hyphema, bleb leak and choroidal detachment. The advantages of injected MMC are primarily in controlling the exact dosage and area of application and reduced surgical time. Lim et al. retrospectively reviewed the outcomes of trabeculectomy in 57 eyes using sponge application directly to the sclera versus intra-tenon injection. IOP was significantly lower in the injection group at 1 month, 1, 2, and 3 years. Trabeculectomy success (IOP<21mm Hg or IOP >20% below baseline without medications or additional surgery) was greater in the injection group at 3 years. The sponge group experienced more encapsulated blebs but complication rates were similar in both groups. To date, there have been no prospective studies comparing the IOP-lowering efficacy and safety of intra-tenon injection versus direct scleral application of MMC.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Open Angle Glaucoma
    Keywords
    trabeculectomy, mitomycin-C, glaucoma

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 4
    Interventional Study Model
    Parallel Assignment
    Masking
    Outcomes Assessor
    Allocation
    Randomized
    Enrollment
    100 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Injection group
    Arm Type
    Active Comparator
    Arm Description
    MMC delivered by preoperative subconjunctival injection
    Arm Title
    Sponge group
    Arm Type
    Active Comparator
    Arm Description
    MMC delivered by intraoperative direct scleral application with impregnated cellulose sponges
    Intervention Type
    Drug
    Intervention Name(s)
    Mitomycin-C injection
    Intervention Description
    MMC delivered by preoperative subconjunctival injection
    Intervention Type
    Drug
    Intervention Name(s)
    Mitomycin-C sponge
    Intervention Description
    MMC delivered by intraoperative direct scleral application with impregnated cellulose sponges
    Primary Outcome Measure Information:
    Title
    Percentage of Participants Achieving Intraocular Pressure Reduction Thresholds
    Description
    Percentage of patients achieving at least a 30% mean intraocular pressure reductions from baseline and with an intraocular pressure <21 mm Hg. Subjects that met this criteria without the use of intraocular pressure lowering medications were classified as "Complete Success." Subjects that met this criteria but required the use of intraocular pressure lowering medications were classified as "Qualified Success." Subjects that failed to meet this criteria were classified as "Failure." Subjects that failed to meet this criteria and required additional glaucoma surgery were classified as "Complete Failure."
    Time Frame
    6 months
    Secondary Outcome Measure Information:
    Title
    Bleb Morphology
    Description
    Bleb morphology at 6 months was graded using Indiana Bleb Appearance Grading Scale. Bleb height was graded on a scale of 0 to 3 (0: flat bleb without visible elevation, 1: low bleb elevation, 2: moderate bleb elevation, 3: high bleb elevation). Bleb extent was graded on a scale of 0 to 3 (0: no visible bleb extent to less than 1 clock hour, 1: extent equal to or greater than 1 clock hour but less than 2 clock hours, 2: extent equal to or greater than 2 clock hours but less than 4 clock hours, 3: extent equal to or greater than 4 clock hours). Bleb vascularity was graded on a scale of 0 to 4 (0: avascular/white, 1: avascular/cystic, 2: mild vascularity, 3: moderate vascularity, 4: extensive vascularity). Scales are descriptive and do not necessarily represent better or worse outcomes.
    Time Frame
    6 months
    Title
    Medications
    Description
    Number of intraocular pressure lowering medications used by the patient at follow up visit.
    Time Frame
    6 months
    Title
    Visual Acuity
    Description
    Change in visual acuity from baseline
    Time Frame
    6 months
    Title
    Number of Participants With Surgical Complications
    Description
    Number of eyes that experienced surgical complications following surgery
    Time Frame
    6 months
    Title
    Number of Participants Requiring Additional Surgery
    Description
    Number of eyes requiring additional surgery from each group
    Time Frame
    6 months
    Title
    Postoperative Interventions
    Description
    Mean number of postoperative interventions (needling, antifibrotic injections) performed in each group
    Time Frame
    6 months

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: medically uncontrolled glaucoma healthy and freely mobile conjunctiva in superior bulbar region Exclusion Criteria: previous incisional glaucoma surgery no light perception vision pregnant or nursing women iris neovascularization or proliferative retinopathy iridocorneal endothelial syndrome chronic or recurrent uveitis steroid-induced glaucoma pathologic myopia or refractive error less than -6.00 diopters unwillingness or inability to give consent inability to return for scheduled protocol visits
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Jiun L Do, MD, PhD
    Organizational Affiliation
    UCSD
    Official's Role
    Principal Investigator
    First Name & Middle Initial & Last Name & Degree
    Robert N Weinreb, MD
    Organizational Affiliation
    UCSD
    Official's Role
    Principal Investigator
    First Name & Middle Initial & Last Name & Degree
    Benjamin Xu, MD, PhD
    Organizational Affiliation
    UCSD
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No

    Learn more about this trial

    Subconjunctival Versus Direct Mitomycin C in Trabeculectomy

    We'll reach out to this number within 24 hrs