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Brimonidine for Oculofacial Surgery
Phase 4
Recruiting
Led By Christopher Compton, MD
Research Sponsored by University of Louisville
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Ophthalmic conditions requiring oculoplastic surgery
Above the age of 18
Must not have
History of Central Nervous System (CNS) depression from medication use
Hypotony
Timeline
Screening 3 weeks
Treatment Varies
Follow Up at the time of surgery.
Awards & highlights
Drug Has Already Been Approved
No Placebo-Only Group
Pivotal Trial
Summary
This trial tests if brimonidine eye drops can help control bleeding in patients having eye-related plastic surgery by making blood vessels smaller. Brimonidine has been studied for its effectiveness in reducing bleeding and improving visibility during various eye surgeries, including trabeculectomy, LASIK, and strabismus surgery.
Who is the study for?
This trial is for adults over 18 needing oculoplastic surgery due to conditions like droopy eyelids. It's not suitable for those with eye infections, a history of CNS depression from meds, clotting issues, current brimonidine use, certain asymmetrical eye conditions, very low eye pressure (hypotony), known brimonidine allergy or side effects, a history of low blood pressure (hypotension), orthostatic hypotension, or if pregnant.
What is being tested?
The study is testing the effectiveness of a topical medication called Brimonidine in controlling bleeding during facial surgeries involving the eyes. The goal is to see how well it works when applied directly to the surgical area.
What are the potential side effects?
Brimonidine may cause dry mouth and eyes, fatigue, headache, dizziness; rarely can lead to lowered heart rate or blood pressure. Side effects are generally mild but vary between individuals.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I need eye surgery due to a condition.
Select...
I am older than 18 years.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I have experienced brain fog or drowsiness from medication.
Select...
I have low eye pressure.
Select...
I experience significant drops in blood pressure when standing up.
Select...
I have a history of low blood pressure.
Select...
I currently have an eye infection.
Select...
I have a blood clotting disorder.
Select...
I am currently using brimonidine.
Select...
I have an eye condition affecting tear drainage.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ at the time of surgery.
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~at the time of surgery.
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Hemostatic function
Side effects data
From 2013 Phase 4 trial • 376 Patients • NCT020035346%
Conjunctiva Hyperemia
100%
80%
60%
40%
20%
0%
Study treatment Arm
0.15% Brimonidine Tartrate
Awards & Highlights
Drug Has Already Been Approved
The FDA has already approved this drug, and is just seeking more data.
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Pivotal Trial
The final step before approval, pivotal trials feature drugs that have already shown basic safety & efficacy.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Brimonidine interventionExperimental Treatment1 Intervention
We will compare hemostasis between 2 surgical sides of the same patient. One side will be randomized to receive Brimonidine (0.15% or 0.2%) in addition to standard hemostasis measures, while the other side will receive only standard hemostasis measures (preoperative discontinuation of blood thinners, preoperative injection of lidocaine with epinephrine).
Group II: Control ArmActive Control1 Intervention
We will compare hemostasis between 2 surgical sides of the same patient. One side will be randomized to receive Brimonidine (0.15% or 0.2%) in addition to standard hemostasis measures, while the other side will receive only standard hemostasis measures (preoperative discontinuation of blood thinners, preoperative injection of lidocaine with epinephrine).
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Entropion, a condition where the eyelid turns inward, can be treated through various methods including lubricating eye drops, botulinum toxin injections, and surgical procedures. Lubricating eye drops help to protect the cornea and reduce irritation.
Botulinum toxin injections temporarily paralyze the muscles causing the inward turning of the eyelid, providing relief from symptoms. Surgical procedures aim to tighten or reposition the eyelid to correct its alignment.
While Brimonidine is primarily used for its vasoconstrictive properties and to reduce intraocular pressure in glaucoma, its mechanism of reducing blood flow and aqueous production is not directly applicable to Entropion treatment. However, understanding these mechanisms is crucial as they highlight the importance of targeted therapies in managing specific ocular conditions effectively.
Ocular perfusion pressure and visual field indice modifications induced by alpha-agonist compound (clonidine 0.125%, apraclonidine 1.0% and brimonidine 0.2%) topical administration. An acute study on primary open-angle glaucoma patients.Effects of a topical alpha2 adrenergic agonist on ciliary blood flow and aqueous production in rabbits.
Ocular perfusion pressure and visual field indice modifications induced by alpha-agonist compound (clonidine 0.125%, apraclonidine 1.0% and brimonidine 0.2%) topical administration. An acute study on primary open-angle glaucoma patients.Effects of a topical alpha2 adrenergic agonist on ciliary blood flow and aqueous production in rabbits.
Find a Location
Who is running the clinical trial?
University of LouisvilleLead Sponsor
345 Previous Clinical Trials
77,315 Total Patients Enrolled
Christopher Compton, MDPrincipal InvestigatorUniversity of Louisville
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I have experienced brain fog or drowsiness from medication.I experience significant drops in blood pressure when standing up.I am older than 18 years.You have had bad reactions to brimonidine in the past.I have a history of low blood pressure.I have low eye pressure.I need eye surgery due to a condition.I currently have an eye infection.I have a blood clotting disorder.I am currently using brimonidine.I have an eye condition affecting tear drainage.
Research Study Groups:
This trial has the following groups:- Group 1: Control Arm
- Group 2: Brimonidine intervention
Awards:
This trial has 3 awards, including:- Drug Has Already Been Approved - The FDA has already approved this drug, and is just seeking more data.
- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
- Pivotal Trial - The final step before approval, pivotal trials feature drugs that have already shown basic safety & efficacy.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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