NCT00713076

Brief Summary

Measure wettability of hydrogel and silicone hydrogel contact lenses presoaked in a Multi-Purpose Solution.

Trial Health

80
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
30

participants targeted

Target at below P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

October 1, 2007

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 1, 2008

Completed
4 months until next milestone

First Submitted

Initial submission to the registry

June 18, 2008

Completed
23 days until next milestone

First Posted

Study publicly available on registry

July 11, 2008

Completed
Last Updated

August 20, 2014

Status Verified

July 1, 2008

Enrollment Period

5 months

First QC Date

June 18, 2008

Last Update Submit

August 18, 2014

Conditions

Vision

Keywords

multi-purpose solutioncontact lens wearersContact lense wearers

Outcome Measures

Primary Outcomes (1)

  • Lens Wettability - ex-vivo wetting angle

    From baseline

Secondary Outcomes (1)

  • Slit-lamp findings Corrected visual acuity (snellen) Adverse events

    From baseline

Study Arms (1)

1

EXPERIMENTAL

Polyquaternium-preserved Multi-purpose solution

Other: Polyquaternium-preserved Multi-purpose Lens Cleaning Solution 109182

Interventions

Polyquaternium-preserved Multi-purpose Lens Cleaning Solution 109182OTHER

Lens Cleaning Solution Formulation Identification Number 109182

1

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Subjects with normal eyes who have successfully worn contact lenses on a daily basis for at least two weeks prior to the study.
  • Must be wearing lenses a minimum of eight hours a day
  • Vision must be correctable to 20/30 (snellen) or better in each eye at a distance with soft contact lenses
  • Use no topical ocular OTC or prescribed ocular medication

You may not qualify if:

  • Subjects using systemic medications, upper respiratory infections or colds, history of seasonal allergies with significant ocular side effects

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Contact Alcon Call Center for Study Locations

Fort Worth, Texas, 76134, United States

Location

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Sponsor Type
INDUSTRY
Responsible Party
SPONSOR

Study Record Dates

First Submitted

June 18, 2008

First Posted

July 11, 2008

Study Start

October 1, 2007

Primary Completion

March 1, 2008

Last Updated

August 20, 2014

Record last verified: 2008-07

Locations

US(1)