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Trial registered on ANZCTR
Registration number
ACTRN12612000143820
Ethics application status
Not yet submitted
Date submitted
26/01/2012
Date registered
1/02/2012
Date last updated
1/02/2012
Type of registration
Prospectively registered
Titles & IDs
Public title
Under-Recognition of Allergic conjunctivitis in Patients with Allergic Rhinitis
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Scientific title
The Effect of Olopatadine Hydrochloride on total ocular symptoms score in Non-allergic conjunctivitis/rhinitis individuals.
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Secondary ID [1]
279801
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n/a
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Allergic rhinitis
285682
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allergic conjunctivitis
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Condition category
Condition code
Eye
285869
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0
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Diseases / disorders of the eye
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Participants will be asked about their indirect symptoms of AC (squinting, blinking, frontal headaches or eyelid dermatitis) to assess whether they suffer. Then total Ocular Symptom Score (TOSS) (tearing, itching and eye redness) will be assessed.
Then, one drop of olopatadine hydrochloride to each eye, ONCE ONLY.
Then 5 minutes will pass before assessing TOSS again.
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Intervention code [1]
284127
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Treatment: Drugs
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Comparator / control treatment
Control group will be used to determine if the lubricating effects of the olopatadine eye drops is acting as the relieving factor in the intervention group
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Control group
Active
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Outcomes
Primary outcome [1]
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Total ocular symptoms score
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Assessment method [1]
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Timepoint [1]
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pre-administration of olopatadine hydrochloride and then at 5minutes post-administration to detect a change in total ocular symptoms score
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Secondary outcome [1]
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nil
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Assessment method [1]
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Timepoint [1]
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nil
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Eligibility
Key inclusion criteria
No allergic conjunctivitis
Over 18 years
Not pregnant
CONFIRMED PARTICIPANTS CANT HAVE AR/AC
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Minimum age
18
Years
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Maximum age
75
Years
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Sex
Both males and females
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Can healthy volunteers participate?
Yes
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Key exclusion criteria
allergic conjunctivitis/rhinitis
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Non-randomised trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Patients attending an allergist's outpatients clinic are asked if they would like to participate in this study. if they consent, then they are assessed for symptoms and signs of allergic conjunctivitis. If they do not have any history or symptoms, then they are administered olopatadine hydrochloride to determine if they improved total ocular symptoms scores in patients without allergic conjunctivitis.
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
no randomisation
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Masking / blinding
Open (masking not used)
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Who is / are masked / blinded?
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Intervention assignment
Single group
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Other design features
nil
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Phase
Not Applicable
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Not yet recruiting
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Date of first participant enrolment
Anticipated
13/02/2012
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Actual
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
20
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
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Funding & Sponsors
Funding source category [1]
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Self funded/Unfunded
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Name [1]
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A/Prof Peter Smith
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Address [1]
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Pacific Private Clinic
123 Nerang St
Southport
Queensland 4215
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Country [1]
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Australia
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Primary sponsor type
Individual
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Name
A/Prof Peter Smith
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Address
Pacific Private Clinic
123 Nerang St
Southport
Q 4215
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Country
Australia
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Secondary sponsor category [1]
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None
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Name [1]
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nil
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Address [1]
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nil
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Country [1]
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Australia
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Ethics approval
Ethics application status
Not yet submitted
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Ethics committee name [1]
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Ethics committee address [1]
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Ethics committee country [1]
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Date submitted for ethics approval [1]
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06/02/2012
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Approval date [1]
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Ethics approval number [1]
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Summary
Brief summary
Aim: To determine the most effective way of detecting the incidence of allergic conjunctivitis (AC). Method: The first step includes asking patients in an allergy specialist's outpatient clinic about their Total Ocular Symptom Score (tearing, itching and eye redness), then asking them about indirect symptoms of AC (squinting, blinking, frontal headaches or eyelid dermatitis), and finally using an olopatadine challenge to determine if any chronic, undetected symptoms of AC are relieved and thus suffered. A control group will be used to determine if the lubricating effects of the olopatadine eye drops is acting as the relieving factor in the intervention group.
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Trial website
n/a
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Address
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Country
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Phone
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Fax
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Email
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Contact person for public queries
Name
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A/Prof Peter Smith
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Address
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Pacific Private Clinic
Level 5 123 Nerang St
Southport
Queensland 4215
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Country
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Australia
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Phone
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+617 5591 5744
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Fax
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Email
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[email protected]
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Contact person for scientific queries
Name
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A/Prof Peter Smith
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Address
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Pacific Private Clinic
Level 5 123 Nerang St
Southport
Queensland 4215
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Country
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Australia
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Phone
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+617 5591 5744
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Fax
7861
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Email
7861
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[email protected]
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No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
No additional documents have been identified.
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