The Use of Amniotic Membrane or Internal Limiting Membrane for Large or Refractory Macular Holes:… (NCT04904679) | Clinical Trial Compass
Active — Not RecruitingNot Applicable
The Use of Amniotic Membrane or Internal Limiting Membrane for Large or Refractory Macular Holes: A Prospective Study
Brazil23 participantsStarted 2020-06-26
Plain-language summary
Prospective, randomized, unmasked interventional study. To evaluate anatomical and functional results through microperimetry in cases of refractory or large macular holes (MH), using amniotic membrane (AM) or internal limiting membrane ( ILM ).
Who can participate
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Patients with a macula hole that falls into the two categories below:
* Patients with idiopathic macular hole (with no history of secondary macular hole) ≥ 600 microns (measured using optical coherence tomography)
* Patients with an idiopathic macular hole submitted to conventional treatment without closing it (of any size).
* History of the disease less than 18 months
* Aged over 18 years old
* Visual acuity less than 20/32
Exclusion Criteria:
* History of any previous macular disease other than idiopathic macular hole
* Macular hole of other causes (secondary)
* Patients with diabetic retinopathy or other retinal vascular diseases
* Eyes subjected to intravitreal injection of any medication
* Visual acuity \<20/400 of any retinal cause in the contralateral eye or absence of the globe \*Aged under 50 years old
* Cataract and anti-glaucoma surgery less than 3 months before the study
* Glaucoma with optic nerve excavation \> 0.7 in the studied eye
* Intraocular pressure \> 24 mmHg with the use of maximum medication in the studied eye
* History of vitreoretinal surgery for a condition other than the idiopathic macular hole (retinal detachment, vitreous hemorrhage)
* History of retinal detachment of any etiology
* A patient who manifests himself not being able to perform the head position in the postoperative period
* A patient with active anterior or posterior uveitis
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
The retinal sensitivity
Timeframe: through study completion, an average of 1 year
2
The fixation stability
Timeframe: through study completion, an average of 1 year