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Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/study/NCT05741216




Registration number
NCT05741216
Ethics application status
Date submitted
14/02/2023
Date registered
23/02/2023
Date last updated
11/10/2023

Titles & IDs
Public title
Evaluation of Comfort of Ocular Lubricants in Symptomatic Contact Lens Wearers
Scientific title
Evaluation of Comfort of Ocular Lubricants in Symptomatic Contact Lens Wearers
Secondary ID [1] 0 0
DEJ475-E006
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Dry Eye 0 0
Condition category
Condition code
Eye 0 0 0 0
Diseases / disorders of the eye

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Other interventions - OTF Ocular Lubricant
Other interventions - Ocular Lubricant

Experimental: OTF Test 1 - One application of ocular lubricant to each eye at night for 5 consecutive nights

Experimental: OTF Test 2 - One application of ocular lubricant to each eye at night for 5 consecutive nights

Experimental: OTF Test 3 - One application of ocular lubricant to each eye at night for 5 consecutive nights

Active comparator: Ocular lubricant - One drop of ocular lubricant applied to each eye at night for 5 consecutive nights


Other interventions: OTF Ocular Lubricant
Ocular lubricant in 1 of 3 test formulations

Other interventions: Ocular Lubricant
Commercially available ocular lubricant

Intervention code [1] 0 0
Other interventions
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
Ocular comfort
Timepoint [1] 0 0
Up to Day 5

Eligibility
Key inclusion criteria
Key

* Is able to understand and sign an approved information consent letter;
* Habitually wears daily disposable soft contact lenses in both eyes
* Uses rewetting drops on a regular basis;
* Other protocol-defined inclusion criteria may apply.

Key
Minimum age
18 Years
Maximum age
No limit
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
* Routinely sleeps in habitual contact lenses;
* Has any known active ocular disease and/or infection;
* Is pregnant or lactating;
* Other protocol specified exclusion criteria may apply.

Study design
Purpose of the study
Treatment
Allocation to intervention
Randomised controlled trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Masking / blinding
Open (masking not used)
Who is / are masked / blinded?



Intervention assignment
Parallel
Other design features
Phase
Not applicable
Type of endpoint/s
Statistical methods / analysis

Recruitment
Recruitment status
Completed
Data analysis
Reason for early stopping/withdrawal
Other reasons
Date of first participant enrolment
Anticipated
Actual
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
Actual
Sample size
Target
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)
NSW,VIC
Recruitment hospital [1] 0 0
School of Optometry and Vision - Sydney
Recruitment hospital [2] 0 0
Deakin Collaborative Eye Care Clinic, Deakin University - Waurn Ponds
Recruitment postcode(s) [1] 0 0
2052 - Sydney
Recruitment postcode(s) [2] 0 0
3216 - Waurn Ponds
Recruitment outside Australia
Country [1] 0 0
Canada
State/province [1] 0 0
Ontario

Funding & Sponsors
Primary sponsor type
Commercial sector/industry
Name
Alcon Research
Address
Country

Ethics approval
Ethics application status

Summary
Brief summary
The purpose of this study is to evaluate the ocular comfort of 3 ocular lubricants and a comparator.
Trial website
https://clinicaltrials.gov/study/NCT05741216
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 0 0
Clinical Trial Lead, Dry Eye
Address 0 0
Alcon Research, LLC
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for public queries
Name 0 0
Address 0 0
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for scientific queries



Summary Results

For IPD and results data, please see https://clinicaltrials.gov/study/NCT05741216