search
Back to results

Safety Study of the Use of Topical Cyclosporine in the Treatment of Dry Eye Disease

Primary Purpose

Primary Sjogren Syndrome, Secondary Sjogren Syndrome, Aqueous Deficient Dry Eye Disease

Status
Completed
Phase
Phase 4
Locations
Brazil
Study Type
Interventional
Intervention
Restasis
Refresh Endura
Sponsored by
Federal University of São Paulo
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Primary Sjogren Syndrome focused on measuring Evaporative, Aqueous deficient, Dry eye disease

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients diagnosed for mild to moderate Aqueous Deficient DED (ADDED), defined as Schirmer 1 < 10mm;
  • Patients diagnosed for mild to moderate Evaporative DED (EDED), defined as normal Schirmer 1 and BUT < 5 seconds;
  • Patients submitted to refractive surgery,
  • Patients capable of understanding instructions, signing the term of consent and available to attend all exam visits.

Exclusion Criteria:

  • patients with punctual occlusion,
  • active ocular infection or inflammatory disease,
  • history of herpetic keratitis,
  • contact lens use during trial period,
  • patients with glaucoma,
  • any eyelid globe malposition abnormality.

Sites / Locations

  • Departamento de Oftalmologia da Escola Paulista de Medicina - UNIFESP

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Refresh Endura

Restasis

Arm Description

Topical lubricant containing (glycerin; polysorbate 80; castor oil; carbomer, boric acid, sodium hydroxide, purified water), one drop 2 times a day, for 3 months.

Topical immunomodulatory lubricant (Ophthalmic emulsion containing cyclosporine 0.5 mg/mL, i.e., 0.05%), one drop 2 times a day, for 3 months

Outcomes

Primary Outcome Measures

Ocular surface inflammation

Secondary Outcome Measures

Full Information

First Posted
December 3, 2013
Last Updated
September 20, 2020
Sponsor
Federal University of São Paulo
Collaborators
Allergan
search

1. Study Identification

Unique Protocol Identification Number
NCT02004067
Brief Title
Safety Study of the Use of Topical Cyclosporine in the Treatment of Dry Eye Disease
Official Title
Safety Study of the Use of Topical Cyclosporine in the Treatment of Dry Eye Disease
Study Type
Interventional

2. Study Status

Record Verification Date
September 2020
Overall Recruitment Status
Completed
Study Start Date
January 2013 (undefined)
Primary Completion Date
August 2016 (Actual)
Study Completion Date
August 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Federal University of São Paulo
Collaborators
Allergan

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
In the present study the investigators aim to determine the efficacy of an immunomodulating topical medication, compared with a topical lubricant, on the treatment of dry eye disease (DED) due to primary or secondary Sjögren's syndrome (aqueous deficient DED) and evaporative DED.
Detailed Description
Dry eye disease (DED) is a multifactorial disease of the tears and ocular surface that results in symptoms of discomfort, visual disturbance, and tear film instability with potential damage to the ocular surface. It is accompanied by increased osmolarity of the tear film and inflammation of the ocular surface. DED prevalence is estimated around 15 -35% of the population over 50 years old. There is a wide variety of topic medications for the treatment of DED, though few aim the re-establishment of tear osmolarity equilibrium and reduction of damages to the ocular surface. The treatment of DED can include a medical treatment, such as tear substitution, tear preservation, production stimulation, anti-inflammatory; it can also include surgical treatment, as tarsorrhaphy and salivary gland transplant. Considering tear substitutes and anti-inflammatory topical treatments, the purpose of our study is to determine efficacy of an immunomodulating topical medication containing 0.05% cyclosporine A (CsA), compared to a topical lubricant (vitamin A, Refresh Endura®), on the treatment of dry eye disease (DED) due to primary or secondary Sjögren's syndrome (aqueous deficient DED) and evaporative DED.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Primary Sjogren Syndrome, Secondary Sjogren Syndrome, Aqueous Deficient Dry Eye Disease, Evaporative Dry Eye Disease
Keywords
Evaporative, Aqueous deficient, Dry eye disease

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Refresh Endura
Arm Type
Active Comparator
Arm Description
Topical lubricant containing (glycerin; polysorbate 80; castor oil; carbomer, boric acid, sodium hydroxide, purified water), one drop 2 times a day, for 3 months.
Arm Title
Restasis
Arm Type
Experimental
Arm Description
Topical immunomodulatory lubricant (Ophthalmic emulsion containing cyclosporine 0.5 mg/mL, i.e., 0.05%), one drop 2 times a day, for 3 months
Intervention Type
Drug
Intervention Name(s)
Restasis
Other Intervention Name(s)
Cyclosporine 0.05%
Intervention Description
Restasis is an ophthalmic emulsion containing cyclosporine 0.5 mg/mL, produced by Allergan Inc.
Intervention Type
Drug
Intervention Name(s)
Refresh Endura
Other Intervention Name(s)
Castor oil
Intervention Description
Refresh Endura is a topical lubricant produced by Allergan, Inc.
Primary Outcome Measure Information:
Title
Ocular surface inflammation
Time Frame
3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients diagnosed for mild to moderate Aqueous Deficient DED (ADDED), defined as Schirmer 1 < 10mm; Patients diagnosed for mild to moderate Evaporative DED (EDED), defined as normal Schirmer 1 and BUT < 5 seconds; Patients submitted to refractive surgery, Patients capable of understanding instructions, signing the term of consent and available to attend all exam visits. Exclusion Criteria: patients with punctual occlusion, active ocular infection or inflammatory disease, history of herpetic keratitis, contact lens use during trial period, patients with glaucoma, any eyelid globe malposition abnormality.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Rossen M Hazarbassanov, PhD
Organizational Affiliation
Federal University of São Paulo
Official's Role
Principal Investigator
Facility Information:
Facility Name
Departamento de Oftalmologia da Escola Paulista de Medicina - UNIFESP
City
Sao Paulo
State/Province
SP
ZIP/Postal Code
04023 062
Country
Brazil

12. IPD Sharing Statement

Plan to Share IPD
Undecided

Learn more about this trial

Safety Study of the Use of Topical Cyclosporine in the Treatment of Dry Eye Disease

We'll reach out to this number within 24 hrs