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
About this trial
This is an interventional treatment trial for Open Angle Glaucoma focused on measuring trabeculectomy, mitomycin-C, glaucoma
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
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
NCT ID
NCT04352660
First Posted
April 15, 2020
Last Updated
June 14, 2020
Sponsor
University of California, San Diego
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
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Subconjunctival Versus Direct Mitomycin C in Trabeculectomy
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