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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.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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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.

Poland1 site
  • Medical University of Lublin

    Lublin, Lublin Voivodeship, 20-059

Other trials in Poland

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:

  1. Open angle glaucoma or capsular glaucoma.
  2. Patient's age> 40 years
  3. Local treatment ineffective due to:
  4. intraocular pressure more than 21mmHg with maximum pharmacological therapy (using B-blocker + carbonic anhydrase + prostaglandins) or
  5. intolerance to topical treatment or
  6. progression in the visual field examination (assessed on the basis of MD, PSD).
  7. Lack of previous ophthalmological surgical interventions.
  8. No previous laser gonioplasty.
  9. No previous laser trabeculoplasty or laser trabeculoplasty performed for more than a year.

Exclusion criteria:

  1. Patient with angle-closure glaucoma or secondary glaucoma (except for glaucoma in the course of pseudoexfoliation syndrome).
  2. One-eye patient.
  3. A patient with pseudophakia or aphakia.
  4. Patient after previous ophthalmic procedures (phacoemulsification with intraocular lens implantation, traditional pars plana vitrectomy, keratoplasty).
  5. A patient diagnosed or suspected of having uveitis or intraocular inflammation.
  6. 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.
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 groups in NCT03766425
Study groupRoleWhat they receive
AfliberceptExperimentalAflibercept 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
MitomycinActive comparatorMitomycin 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.

  1. 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

  2. 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)
  1. 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

  2. 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

  3. 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

  4. 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.

  1. First posted6 Dec 2018
  2. Study start14 Jun 2017
  3. Primary completion31 Jul 2019
  4. Study completion31 Jul 2019

Resources

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)
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

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.

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