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The Effects of BAK on the Blood Aqueous Barrier of Pseudophakic Patients

Primary Purpose

Dry Eye Syndromes

Status
Completed
Phase
Phase 4
Locations
Brazil
Study Type
Interventional
Intervention
Hydroxypropylmethylcellulose
Carboxymethylcellulose
Sponsored by
University of Campinas, Brazil
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Dry Eye Syndromes focused on measuring dry eye, pseudophakia, cornea, lubricating drop, BAK, blood aqueous barrier, blood-retina barrier

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Pseudophakic eyes that underwent cataract surgery at least 6 months before.

Exclusion Criteria:

  • Use of any eyedrop.
  • Other conditions associated with a break in the blood-aqueous or blood retina barrier (ie diabetes, ARMD, vasculitis, uveitis)
  • Previous history of cystoid macular edema.
  • Previous ocular surgery other than cataract surgery.

Sites / Locations

  • Department of Ophthalmology, University of Campinas

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Preserved (BAK 0.006%) lubricating drop

Preservative-free lubricating drops

Arm Description

One group will receive preserved lubricating drops 4 times a day for 1 month.

The second group will receive preservative-free lubricating drops 4 times a day for 1 month.

Outcomes

Primary Outcome Measures

Aqueous Humor Flare
Aqueous humor flare indicates the degree of a break in the blood-aqueous barrier. It is objectively measured with a Laser flare meter.

Secondary Outcome Measures

Macular Thickness
Macular thickness will be measured with an Optical coherence tomography (OCT). Measures 5% under the normal population according to the OCT software will be considered break in the blood-retina barrier.

Full Information

First Posted
January 18, 2011
Last Updated
July 12, 2012
Sponsor
University of Campinas, Brazil
Collaborators
Merck Sharp & Dohme LLC
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1. Study Identification

Unique Protocol Identification Number
NCT01280110
Brief Title
The Effects of BAK on the Blood Aqueous Barrier of Pseudophakic Patients
Official Title
The Effects of BAK on the Blood Aqueous Barrier of Pseudophakic Patients
Study Type
Interventional

2. Study Status

Record Verification Date
July 2012
Overall Recruitment Status
Completed
Study Start Date
March 2011 (undefined)
Primary Completion Date
December 2011 (Actual)
Study Completion Date
January 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Campinas, Brazil
Collaborators
Merck Sharp & Dohme LLC

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
BAK is one of the most frequent preservatives in eye drops. BAK is a quaternary ammonium salt with surfactant qualities. It can be bacteriostatic or bactericidal depending on the concentrations used. It has been shown to be effective against most bacteria with a few exceptions, such as Pseudomonas aeruginosa, or picornaviruses. It as been widely used in eyedrops, nose sprays, hand and face washes, mouthwashes, spermicidal creams, and in various other cleaners, sanitizers, and disinfectants. BAK gained popularity when it was first introduced because it also enhances corneal penetration of some drugs by causing epithelial separation. It is present in several ophthalmic formulations, including most of the antiglaucoma medications. If used chronically, BAK has been found to cause ocular surface changes, such as dry eye and punctuate keratitis. BAK has also been suggested to promote a break in the blood aqueous barrier, which may lead to undesirable consequences, such as uveitis and cystoid macular edema. However, this information is controversial. The purpose of this study is to evaluate the consequences of BAK on the blood-retinal and blood-aqueous barriers of pseudophakic patients receiving BAK-preserved lubricating drops.
Detailed Description
The primary hypothesis behind the study is that BAK may lead to a break in the blood-retina barrier in pseudophakic eyes, leading to an increase in macular thickness, compared to a non-BAK containing solution. The secondary hypothesis is that solutions containing BAK will increase the permeability of the blood aqueous barrier compared to non-BAK solutions. If the hypotheses are confirmed, they may serve as a contraindication to the use of BAK-preserved drops in pseudophakic eyes requiring chronic use of medications. This is a prospective, randomized, examiner-masked, controlled study involving 44 pseudophakic eyes of 44 patients. Patients receiving any other eyedrop, with a previous history of uveitis, posterior capsule rupture or any other ophthalmic surgery will be excluded. Patients will be randomized to the use of a BAK-preserved lubricating drop or to the use of a non-preserved lubricating drop q.i.d for one month. Effects on the blood aqueous barrier will be objectively measured with a laser flare meter (Kowa, Japan) at baseline, 15 days and one month after inclusion. Patients will also have OCT images (Cirrus, Zeiss, USA) of the macula at the same time intervals to evaluate the possible effects on the blood-retina barrier. Macular thickness and the presence of cystoid macular edema will be evaluated at each time interval.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Dry Eye Syndromes
Keywords
dry eye, pseudophakia, cornea, lubricating drop, BAK, blood aqueous barrier, blood-retina barrier

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
44 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Preserved (BAK 0.006%) lubricating drop
Arm Type
Active Comparator
Arm Description
One group will receive preserved lubricating drops 4 times a day for 1 month.
Arm Title
Preservative-free lubricating drops
Arm Type
Active Comparator
Arm Description
The second group will receive preservative-free lubricating drops 4 times a day for 1 month.
Intervention Type
Drug
Intervention Name(s)
Hydroxypropylmethylcellulose
Other Intervention Name(s)
Retin Active
Intervention Description
22 patients will receive this lubricating drop 4 times a day for 1 month
Intervention Type
Drug
Intervention Name(s)
Carboxymethylcellulose
Other Intervention Name(s)
Optive UD
Intervention Description
22 patients will receive this lubricating drop 4 times a day for 1 month.
Primary Outcome Measure Information:
Title
Aqueous Humor Flare
Description
Aqueous humor flare indicates the degree of a break in the blood-aqueous barrier. It is objectively measured with a Laser flare meter.
Time Frame
Baseline, 15 days and 30 days.
Secondary Outcome Measure Information:
Title
Macular Thickness
Description
Macular thickness will be measured with an Optical coherence tomography (OCT). Measures 5% under the normal population according to the OCT software will be considered break in the blood-retina barrier.
Time Frame
Baseline, 15 days and 30 days.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Pseudophakic eyes that underwent cataract surgery at least 6 months before. Exclusion Criteria: Use of any eyedrop. Other conditions associated with a break in the blood-aqueous or blood retina barrier (ie diabetes, ARMD, vasculitis, uveitis) Previous history of cystoid macular edema. Previous ocular surgery other than cataract surgery.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Vital P Costa, MD
Organizational Affiliation
Department of Ophthalmology, University of Campinas
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Ophthalmology, University of Campinas
City
Campinas
State/Province
SP
Country
Brazil

12. IPD Sharing Statement

Citations:
PubMed Identifier
20302969
Citation
Baudouin C, Labbe A, Liang H, Pauly A, Brignole-Baudouin F. Preservatives in eyedrops: the good, the bad and the ugly. Prog Retin Eye Res. 2010 Jul;29(4):312-34. doi: 10.1016/j.preteyeres.2010.03.001. Epub 2010 Mar 17.
Results Reference
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PubMed Identifier
15220734
Citation
Noecker RJ, Herrygers LA, Anwaruddin R. Corneal and conjunctival changes caused by commonly used glaucoma medications. Cornea. 2004 Jul;23(5):490-6. doi: 10.1097/01.ico.0000116526.57227.82.
Results Reference
background
PubMed Identifier
20931366
Citation
Ammar DA, Noecker RJ, Kahook MY. Effects of benzalkonium chloride-preserved, polyquad-preserved, and sofZia-preserved topical glaucoma medications on human ocular epithelial cells. Adv Ther. 2010 Nov;27(11):837-45. doi: 10.1007/s12325-010-0070-1. Epub 2010 Oct 7.
Results Reference
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The Effects of BAK on the Blood Aqueous Barrier of Pseudophakic Patients

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