CompletedPhase 2

Efficacy of Apraclonidine Eye Drops in the Treatment of Ptosis Secondary to Myasthenia Gravis

Lebanon10 participantsStarted 2020-06-01

Plain-language summary

This study is aimed at assessing the efficacy of Apraclonidine eye drops in the treatment of ptosis secondary to myasthenia gravis.

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 aged 18 or older with a diagnosis of ocular or generalized myasthenia gravis with ocular involvement. Exclusion Criteria: * Patients receiving mono-amino-oxidase inhibitors. * Patients with history of hypertension, cardiac, or cerebrovascular disease. * Women with confirmed pregnancy.

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

Change in palpebral fissure height (PF)

Timeframe: Before administration, at 1, 5, 30, and 60 minutes after administration

Change in marginal reflex distance-1 (MRD1)

Timeframe: Before administration, at 1, 5, 30, and 60 minutes after administration

Change in marginal reflex distance-2 (MRD2)

Timeframe: Before administration, at 1, 5, 30, and 60 minutes after administration

Change in levator function (LF)

Timeframe: Before administration, at 1, 5, 30, and 60 minutes after administration

Trial details

NCT IDNCT05045248

SponsorAmerican University of Beirut Medical Center

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2021-04-15

View on ClinicalTrials.gov More Myasthenia Gravis trials

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.

What they're measuring

Change in palpebral fissure height (PF)

Timeframe: Before administration, at 1, 5, 30, and 60 minutes after administration

Change in marginal reflex distance-1 (MRD1)

Timeframe: Before administration, at 1, 5, 30, and 60 minutes after administration

Change in marginal reflex distance-2 (MRD2)

Timeframe: Before administration, at 1, 5, 30, and 60 minutes after administration

Change in levator function (LF)

Timeframe: Before administration, at 1, 5, 30, and 60 minutes after administration