Trial Review

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Trial registered on ANZCTR


Registration number
ACTRN12610001068055
Ethics application status
Approved
Date submitted
1/12/2010
Date registered
3/12/2010
Date last updated
13/05/2014
Type of registration
Prospectively registered

Titles & IDs
Public title
Evaluation of clinical performance of PureVision[Registered trade mark] contact lenses in conjunction with Biotrue[Trade mark] lens care solution
Scientific title
Prospective, open-label, daily wear study of PureVision[Registered trade mark] contact lenses in conjunction with Biotrue[Trade mark] lens care solution to evaluate product performance in terms of lens case contamination and ocular surface effects in both experienced and new contact lens wearers
Secondary ID [1] 253220 0
None
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
contact lens wear 258755 0
ocular comfort 258756 0
Condition category
Condition code
Eye 258903 258903 0 0
Normal eye development and function

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
This is a prospective, single group, daily wear (DW) study where 40 participants will wear PureVision[Registered trade mark] study lenses bilaterally on a daily wear (DW) basis in conjunction with Biotrue [Trade mark] solution for 3 months. There will be a minimum of 5 scheduled visits: baseline, 2 hour visit, 2 week visit, 1 month visit and 3 month visit. These visits will involve assessment of visual acuity, examination with a slit-lamp biomicroscope (a specialised microscope for viewing the eye) and assessment of ocular comfort using questionnaires employing a 1-10 numeric rating scale. Lenses will be worn a minimum of 5 days per week, and 6 hours on the day lenses are worn.
Intervention code [1] 257694 0
Treatment: Devices
Comparator / control treatment
The control for the outcomes of ocular surface effect, and contact lens contamination will be historical data ( Study ACTRN12610000348055). The method of analysis of contact lens cases will be as per historical control
Control group
Historical

Outcomes
Primary outcome [1] 259761 0
Ocular surface effetcs as assessed with a slit lamp biomicroscope, which is a specialised microscope to view the eye
Timepoint [1] 259761 0
2 hours after baseline and after 2 weeks, 1 month and 3 months of DW
Secondary outcome [1] 268523 0
Contamination rate of contact lens cases used with studied solution compared to historical data. The historical data consists of data collected from previous clinical trials run at the Institute for Eye Research from 2005-2009
Timepoint [1] 268523 0
1 month and 3 months

Eligibility
Key inclusion criteria
-Able to read and comprehend English and give informed consent as demonstrated by signing a record of informed consent;
-Be at least 18 years old, male or female;
-Willing to comply with the wearing and clinical trial visit schedule as directed by the investigator;
-Have ocular health findings considered to be “normal” and which would not prevent the participant from safely wearing contact lenses;
-Is correctable to at least 6/12 (20/40) or better in each eye with contact lenses;
-May be experienced or inexperienced at wearing contact lenses.
Minimum age
18 Years
Maximum age
No limit
Sex
Both males and females
Can healthy volunteers participate?
Yes
Key exclusion criteria
-Any pre-existing ocular irritation, injury or condition (including infection or disease) of the cornea, conjunctiva or eyelids that would preclude contact lens fitting and safe wearing of contact lenses;
-Any systemic disease that adversely affects ocular health e.g. diabetes, Graves disease, and auto-immune diseases such as ankylosing spondylitis, multiple sclerosis, Sjögrens syndrome and systemic lupus erythematosus. Conditions such as systemic hypertension and arthritis do not automatically exclude prospective participants;
-Use of or a need for concurrent category S3 and above ocular medication at enrolment and/or during the study;
Use of or a need for any systemic medication or topical medications which may alter normal ocular findings/are known to affect a participant’s ocular health/physiology or contact lens performance either in an adverse or beneficial manner at enrolment and/or during the study;
N.B.: Systemic antihistamines are allowed on an ‘as needed basis’, provided they are not used prophylactically during the trial and at least 24 hours before study product is used;
Eye surgery within 12 weeks immediately prior to enrolment for this trial;
-Previous corneal refractive surgery;
-Contraindications to contact lens wear;
-Known allergy or intolerance to ingredients in any of the study products;
-Currently enrolled in another clinical trial.
-Participation in a clinical trial within the previous 2 weeks for dispensing studies and 48 hours between in-house studies;
-Pregnancy*;

The Investigator may, at his/her discretion, exclude anyone who they believe may not be able to fulfil the study requirements, or if it is believed to be in the participant’s best interests.
*Formal testing of pregnancy is not required. A participant’s verbal report is sufficient.

Study design
Purpose of the study
Treatment
Allocation to intervention
Non-randomised trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Particicpant needs to satisfy inclusion/exclusion criteria. All participants are allocated the same treatment
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
Single group
Other design features
Phase
Type of endpoint/s
Safety/efficacy
Statistical methods / analysis

Recruitment
Recruitment status
Completed
Date of first participant enrolment
Anticipated
12/01/2011
Actual
11/02/2011
Date of last participant enrolment
Anticipated
14/06/2011
Actual
14/06/2011
Date of last data collection
Anticipated
Actual
Sample size
Target
40
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)

Funding & Sponsors
Funding source category [1] 258167 0
Charities/Societies/Foundations
Name [1] 258167 0
Brien Holden Vision Institute
Country [1] 258167 0
Australia
Primary sponsor type
Other Collaborative groups
Name
Abbott Medical Optics, Inc
Address
1700 East St. Andrew Place
PO Box 25162
Santa Ana, CA 92799-5162, USA
Country
United States of America
Secondary sponsor category [1] 257341 0
None
Name [1] 257341 0
Address [1] 257341 0
Country [1] 257341 0

Ethics approval
Ethics application status
Approved
Ethics committee name [1] 260154 0
VIHEC Human Research Ethics Committee
Ethics committee address [1] 260154 0
Level 4, North Wing, Rupert Myers Building (RMB), Gate 14, Barker Street, The University of New South Wales SYDNEY NSW 2052
Ethics committee country [1] 260154 0
Australia
Date submitted for ethics approval [1] 260154 0
Approval date [1] 260154 0
30/11/2010
Ethics approval number [1] 260154 0
10/21

Summary
Brief summary
This study will examine the effect of a new solution on the ocular surface, subjective ratings of comfort and antimicrobial efficacy of the solution by lens-case examination. The hypotheses are these outcomes will be similar to historical control.
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 31977 0
Mr Daniel Tilia
Address 31977 0
Level 5, North Wing, RMB, Gate 14, Barker Street, The University of New South Wales SYDNEY NSW 2052
Country 31977 0
Australia
Phone 31977 0
+61293857516
Fax 31977 0
Email 31977 0
[email protected]
Contact person for public queries
Name 15224 0
Mr Daniel Tilia
Address 15224 0
Level 5, North Wing, RMB, Gate 14, Barker Street, The University of New South Wales SYDNEY NSW 2052
Country 15224 0
Australia
Phone 15224 0
+61293857516
Fax 15224 0
Email 15224 0
[email protected]
Contact person for scientific queries
Name 6152 0
Mr Daniel Tilia
Address 6152 0
Level 5, North Wing, RMB, Gate 14, Barker Street, The University of New South Wales SYDNEY NSW 2052
Country 6152 0
Australia
Phone 6152 0
+61293857516
Fax 6152 0
Email 6152 0
[email protected]

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.