Eye DiseasesEarly Phase 1NCT03766425
Comparison of Efficacy and Safety of Mitomycin and Aflibercept Used to Support Primary Trabeculectomy.
A Early Phase 1 study testing Aflibercept and Mitomycin in people with Eye Diseases and Optic Nerve Damage, run by Medical University of Lublin at 1 site in Poland.
Trial summary
Comparison of efficacy and safety of Mitomycin and Aflibercept used to support primary trabeculectomy - a prospective, randomized trial in patients with open-angle glaucoma undergoing surgery. Read more about this study
- Who is it for?
- Ages 40 years and older
- Conditions the study is for
- Eye Diseases, Optic Nerve Damage, Glaucoma Surgery
- What is being tested?
- Aflibercept and Mitomycin
- Type of treatment
- Injection or infusion
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 64 participants
- Where
- 1 sitePoland
- Study dates
- 14 Jun 2017to 31 Jul 2019
- Phase
- Early Phase 1
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 40 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Primary open-angle glaucoma or capsular glaucoma.
- Patient's age: over 40 years, no sex preference;
- Local treatment ineffective due to:
- Intraocular pressure above 21mmHg at maximum pharmacological therapy (using β-blocker + carbonic anhydrase inhibitor + prostaglandins) or
- Intolerance to topical treatment or
- Progression in visual field examination
Show all 9Show fewer
- Lack of previous ophthalmological surgical interventions.
- Lack of previously performed laser gonioplasty.
- No laser trabeculoplasty or laser trabeculoplasty performed for more than a year.
Who cannot join
- Patient with primary closed-angle glaucoma or secondary glaucoma (except for glaucoma in the course of pseudoexfoliation syndrome).
- One-eye patient.
- Patient with aphakia.
- Patient after previous ophthalmic procedures (cataract removal by phacoemulsification with an implant of an intraocular lens, vitrectomy by pars plana, keratoplasty).
- A patient diagnosed or suspected of having uveitis or intraocular inflammation.
- Any corneal abnormalities or other conditions that prevent reliable testing with an applanation device in the treated eye, including earlier refractive surgery of the eye.
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Comparison of Efficacy and Safety of Mitomycin and Aflibercept Used to Support Primary Trabeculectomy - a Prospective, Randomized Trial in Patients With Open-angle Glaucoma Undergoing Surgery.
Comparison of efficacy and safety of Mitomycin and Aflibercept used to support primary trabeculectomy - a prospective, randomized trial in patients with open-angle glaucoma undergoing surgery.
Read the detailed description
Glaucoma is a neurodegenerative disease characterized by progressive dying of retinal ganglion cells, axonal loss and damage to the optic nerve. This leads to a gradual loss of the visual field, and in the final stage to blindness. High intraocular pressure is considered to be the main risk factor for glaucomatous neuropathy. In the treatment we use pharmacological therapies and surgical treatment. The trabeculectomy has been the golden standard for the treatment of glaucoma for many years. This procedure consisting in the creation of a filtering bleb, which allows drainage of aqueous humor from within the eye to underneath the conjunctiva where it is absorbed. in addition to the surgery, anti-proliferative substances play a significant role in suppressing the physiological healing process. Bleb insufficiency observed in the postoperative period results to a large extent from progressive scarring of the follicle, which is responsible for excessive fibroblast proliferation and subconjunctival fibrosis.
Mitomycin is an antineoplastic antibiotic produced by Streptomyces caespitosus. It is one of the bi- or tri-functional alkylating agents causing cross-linking of DNA and inhibition of DNA synthesis. Its properties cause that mitomycin is now a popular medicine used to support trabeculectomy, with proven effectiveness of inhibiting the unwanted healing process of the fistula, and thus extend its period of its proper functioning.
Aflibercept is an inhibitor of vascular endothelial growth factor (VEGF). Its properties cause inhibition of the pathological process of formation of new vessels and their excessive permeability, as well as reduction of leukocyte infiltration and inflammation.
The aim of the research:
Comparison of the effectiveness of primary trabeculectomy in patients with open angle glaucoma supported with Eylea (Aflibercept) compared to the group of patients treated with mitomycin.
Materials and methods:
The research conducted at the Department of Glaucoma Diagnostics and Microsurgery in Medical University of Lublin will include patients treated with antiproliferative substances and trabeculectomy. Two groups of patients will participate in the study:
Group I - patients qualified for mitomycin trabeculectomy Group II - patients qualified for Eylea assisted trabeculectomy (Aflibercept) Mitomycin will be administered in the first group of patients during an operation at a dose of 0.3mg / ml for 3 minutes on a soaked sponge. Aflibercept will be applied intraoperatively in a dose of of 0.05 ml (40 mg / ml) subconjunctival and one week after surgery in the same dose.
Criteria for inclusion:
- Open angle glaucoma or capsular glaucoma.
- Patient's age> 40 years
- Local treatment ineffective due to:
- intraocular pressure more than 21mmHg with maximum pharmacological therapy (using B-blocker + carbonic anhydrase + prostaglandins) or
- intolerance to topical treatment or
- progression in the visual field examination (assessed on the basis of MD, PSD).
- Lack of previous ophthalmological surgical interventions.
- No previous laser gonioplasty.
- No previous laser trabeculoplasty or laser trabeculoplasty performed for more than a year.
Exclusion criteria:
- Patient with angle-closure glaucoma or secondary glaucoma (except for glaucoma in the course of pseudoexfoliation syndrome).
- One-eye patient.
- A patient with pseudophakia or aphakia.
- Patient after previous ophthalmic procedures (phacoemulsification with intraocular lens implantation, traditional pars plana vitrectomy, keratoplasty).
- A patient diagnosed or suspected of having uveitis or intraocular inflammation.
- Any corneal abnormalities or other conditions that make it impossible to reliably test with an applanation tonometer in the treated eye, including earlier refractive surgery of the eye
The efficacy of surgery in both groups will be assessed at subsequent postoperative controls based on the following diagnostic tests:
- Visual acuity examination;
- Intraocular pressure examination;
- Evaluation of the filtering bleb in the slit lamp;
- A photo of the filtering bleb;
- Optical coherence tomography of the filtration bleb;
- Visual field;
- Study of corneal endothelial cell density.
- Conditions
- Eye Diseases, Optic Nerve Damage, Glaucoma Surgery
- Being tested
- Aflibercept, Mitomycin
- Keywords
- aflibercept, glaucoma, mitomycin, trabeculectomy
- Medical subject headings
- Eye Diseases, Optic Nerve Injuries, Glaucoma
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
AfliberceptDrug
Also called Eylea, Zaltrap
subconjunctival injection
MitomycinDrug
Also called Ametycine, Mit-C, Mitomycin C
subconjunctival injection
| Study group | Role | What they receive |
|---|---|---|
| Aflibercept | Experimental | Aflibercept applied intraoperatively as a subconjunctival injection at a dose of 0.05 ml (40 mg / ml) and one week after the operation at the same dose, also subconjunctival. Receives: Drug: Aflibercept |
| Mitomycin | Active comparator | Mitomycin applied during a surgery at a concentration of 0.3mg / ml for 3 min. on a soaked sponge. Receives: Drug: Mitomycin |
What is being measured
The primary outcome is the main question the study is designed to answer.
Effectiveness of aflibercept and mitomycin on the morphology of the bleb;
Rating the bleb in The Indiana Bleb Appearance Grading Scale, describing bleb height, extent, vascularity, and leakage with the Seidel test.
Measured: 1 year
Effectiveness of aflibercept and mitomycin on the function of the bleb;
Measurement of intraocular pressure (Goldmann applanation tonometer) and taking a photo of a bleb.
Measured: 1 year
Secondary outcomes (4)
Impact of tested substances on visual acuity after surgery
Examination of a visual acuity 1 week after operation as well as 1 month, 3 months, 6 months, 12 months
Measured: 1 year
The influence of aflibercept and mitomycin on corneal endothelial cell density after surgery
Examination of the corneal endothelial cell density before the surgery as well as 6 months and 12 months after surgery
Measured: 1 year
Impact of used substances on visual field parameters
Examination of a visual field in SITA (Swedish Interactive Testing Algorithm) FAST strategy before the surgery and 12 months after surgery
Measured: 1 year
Frequencies and type of possible complications.
observing and recording all complications and side effects in both groups of patients
Measured: 1 year
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted6 Dec 2018
- Study start14 Jun 2017
- Primary completion31 Jul 2019
- Study completion31 Jul 2019
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Eye DiseasesStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Early Phase 1
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind
- Who is masked
- Participant
- Enrolment
- 64 participants (actual)
Sponsor and investigators
- Lead sponsor
- Medical University of Lublin
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Justyna Kaproń-Świś, Medical University of Lublin
- Investigators
- Tomasz Żarnowski, PhD, Study director, Medical Uniwersity of Lublin al. Racławickie 1 20-059 LublinJustyna Kaproń-Swiś, MD, Principal investigator, Medical Uniwersity of Lublin al. Racławickie 1 20-059 Lublin
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT03766425
- Sponsor's protocol ID
- KE-0254/133/2017
- Status last verified
- Oct 2023
- First submitted
- 25 Nov 2018
- Last updated
- 27 Oct 2023
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 27 Oct 2023. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Comparison of Efficacy and Safety of Mitomycin and Aflibercept Used to Support Primary Trabeculectomy - a Prospective, Randomized Trial in Patients With Open-angle Glaucoma Undergoing Surgery.
- ClinicalTrials.gov ID
- NCT03766425
- Acronym / sponsor ID
- KE-0254/133/2017
- Conditions
- Eye Diseases, Optic Nerve Damage, Glaucoma Surgery
- Keywords
- aflibercept, glaucoma, mitomycin, trabeculectomy
- Phase
- Early Phase 1
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 64 participants (actual)
- Lead sponsor
- Medical University of LublinUniversity, hospital or other
- Study start
- 14 Jun 2017 (actual)
- Primary completion
- 31 Jul 2019 (actual)
- Study completion
- 31 Jul 2019 (actual)
- First posted
- 6 Dec 2018 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Comparison of efficacy and safety of Mitomycin and Aflibercept used to support primary trabeculectomy - a prospective, randomized trial in patients with open-angle glaucoma undergoing surgery.
Detailed description
Glaucoma is a neurodegenerative disease characterized by progressive dying of retinal ganglion cells, axonal loss and damage to the optic nerve. This leads to a gradual loss of the visual field, and in the final stage to blindness. High intraocular pressure is considered to be the main risk factor for glaucomatous neuropathy. In the treatment we use pharmacological therapies and surgical treatment. The trabeculectomy has been the golden standard for the treatment of glaucoma for many years. This procedure consisting in the creation of a filtering bleb, which allows drainage of aqueous humor from within the eye to underneath the conjunctiva where it is absorbed. in addition to the surgery, anti-proliferative substances play a significant role in suppressing the physiological healing process. Bleb insufficiency observed in the postoperative period results to a large extent from progressive scarring of the follicle, which is responsible for excessive fibroblast proliferation and subconjunctival fibrosis.
Mitomycin is an antineoplastic antibiotic produced by Streptomyces caespitosus. It is one of the bi- or tri-functional alkylating agents causing cross-linking of DNA and inhibition of DNA synthesis. Its properties cause that mitomycin is now a popular medicine used to support trabeculectomy, with proven effectiveness of inhibiting the unwanted healing process of the fistula, and thus extend its period of its proper functioning.
Aflibercept is an inhibitor of vascular endothelial growth factor (VEGF). Its properties cause inhibition of the pathological process of formation of new vessels and their excessive permeability, as well as reduction of leukocyte infiltration and inflammation.
The aim of the research:
Comparison of the effectiveness of primary trabeculectomy in patients with open angle glaucoma supported with Eylea (Aflibercept) compared to the group of patients treated with mitomycin.
Materials and methods:
The research conducted at the Department of Glaucoma Diagnostics and Microsurgery in Medical University of Lublin will include patients treated with antiproliferative substances and trabeculectomy. Two groups of patients will participate in the study:
Group I - patients qualified for mitomycin trabeculectomy Group II - patients qualified for Eylea assisted trabeculectomy (Aflibercept) Mitomycin will be administered in the first group of patients during an operation at a dose of 0.3mg / ml for 3 minutes on a soaked sponge. Aflibercept will be applied intraoperatively in a dose of of 0.05 ml (40 mg / ml) subconjunctival and one week after surgery in the same dose.
Criteria for inclusion:
- Open angle glaucoma or capsular glaucoma.
- Patient's age> 40 years
- Local treatment ineffective due to:
- intraocular pressure more than 21mmHg with maximum pharmacological therapy (using B-blocker + carbonic anhydrase + prostaglandins) or
- intolerance to topical treatment or
- progression in the visual field examination (assessed on the basis of MD, PSD).
- Lack of previous ophthalmological surgical interventions.
- No previous laser gonioplasty.
- No previous laser trabeculoplasty or laser trabeculoplasty performed for more than a year.
Exclusion criteria:
- Patient with angle-closure glaucoma or secondary glaucoma (except for glaucoma in the course of pseudoexfoliation syndrome).
- One-eye patient.
- A patient with pseudophakia or aphakia.
- Patient after previous ophthalmic procedures (phacoemulsification with intraocular lens implantation, traditional pars plana vitrectomy, keratoplasty).
- A patient diagnosed or suspected of having uveitis or intraocular inflammation.
- Any corneal abnormalities or other conditions that make it impossible to reliably test with an applanation tonometer in the treated eye, including earlier refractive surgery of the eye
The efficacy of surgery in both groups will be assessed at subsequent postoperative controls based on the following diagnostic tests:
- Visual acuity examination;
- Intraocular pressure examination;
- Evaluation of the filtering bleb in the slit lamp;
- A photo of the filtering bleb;
- Optical coherence tomography of the filtration bleb;
- Visual field;
- Study of corneal endothelial cell density.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (participant)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Aflibercept | Experimental | Drug: AfliberceptAflibercept applied intraoperatively as a subconjunctival injection at a dose of 0.05 ml (40 mg / ml) and one week after the operation at the same dose, also subconjunctival. |
| Mitomycin | Active comparator | Drug: MitomycinMitomycin applied during a surgery at a concentration of 0.3mg / ml for 3 min. on a soaked sponge. |
Who may qualify
- Ages
- 40 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (9 listed)
- Primary open-angle glaucoma or capsular glaucoma.
- Patient's age: over 40 years, no sex preference;
- Local treatment ineffective due to:
- Lack of previous ophthalmological surgical interventions.
- Lack of previously performed laser gonioplasty.
Key exclusion criteria (6 listed)
- Patient with primary closed-angle glaucoma or secondary glaucoma (except for glaucoma in the course of pseudoexfoliation syndrome).
- One-eye patient.
- Patient with aphakia.
- Patient after previous ophthalmic procedures (cataract removal by phacoemulsification with an implant of an intraocular lens, vitrectomy by pars plana, keratoplasty).
- A patient diagnosed or suspected of having uveitis or intraocular inflammation.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| AfliberceptAlso: Eylea, Zaltrapsubconjunctival injection | Drug | Aflibercept |
| MitomycinAlso: Ametycine, Mit-C, Mitomycin Csubconjunctival injection | Drug | Mitomycin |
Primary outcome
Effectiveness of aflibercept and mitomycin on the morphology of the bleb;
Time frame: 1 year
Rating the bleb in The Indiana Bleb Appearance Grading Scale, describing bleb height, extent, vascularity, and leakage with the Seidel test.
Effectiveness of aflibercept and mitomycin on the function of the bleb;
Time frame: 1 year
Measurement of intraocular pressure (Goldmann applanation tonometer) and taking a photo of a bleb.
4 secondary outcomes
Impact of tested substances on visual acuity after surgery
Time frame: 1 year
The influence of aflibercept and mitomycin on corneal endothelial cell density after surgery
Time frame: 1 year
Impact of used substances on visual field parameters
Time frame: 1 year
Frequencies and type of possible complications.
Time frame: 1 year
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 27 Oct 2023.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Tomasz Żarnowski, PhD study director
Medical Uniwersity of Lublin al. Racławickie 1 20-059 Lublin
Justyna Kaproń-Swiś, MD principal investigator
Medical Uniwersity of Lublin al. Racławickie 1 20-059 Lublin
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Early Phase 1 study testing Aflibercept and Mitomycin in people with Eye Diseases and Optic Nerve Damage, run by Medical University of Lublin at 1 site in Poland.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 9 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 27 Oct 2023. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Poland. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Early Phase 1 (sometimes called Phase 0) studies give a very small amount of a treatment to a few people, mainly to see how the body handles it.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Effectiveness of aflibercept and mitomycin on the morphology of the bleb; (time frame: 1 year). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 27 Oct 2023.