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Dry EyeNCT00673855

Acute Comfort of Lubricant Eye Drops FID 112903

A study testing Lubricant Eye Drops FID 112903 and Optive Lubricant Eye Drops in people with Dry Eye, run by Alcon Research at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

To evaluate the acute comfort and blurring profile between two artificial tears in dry eye patients. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Dry Eye
What is being tested?
Lubricant Eye Drops FID 112903 and Optive Lubricant Eye Drops
Could I receive a placebo?
No, everyone receives an active treatment
How many people
20 participants
Where
1 siteUnited States
Study dates
May 2008to May 2008
Phase
Interventional
Are there results?
Yes, posted in the registrySummary in the doctors' view

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Documented diagnosis of dry eye
  • Must not have worn contact lenses for 1 week preceding enrollment

Who cannot join

  • Age related

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Mansfield

    Mansfield, Texas, 76134

Other trials in United States

About this study

To evaluate the acute comfort and blurring profile between two artificial tears in dry eye patients.

Conditions
Dry Eye
Being tested
Lubricant Eye Drops FID 112903, Optive Lubricant Eye Drops
Keywords
Dry eye, Artificial tear
Medical subject headings
Dry Eye Syndromes

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Lubricant Eye Drops FID 112903Other

    Lubricant Eye Drops FID 112903 1 drop each eye 1 time

  • Optive Lubricant Eye DropsOther

    Optive Lubricant Eye Drops

Study groups in NCT00673855
Study groupRoleWhat they receive
Lubricant Eye Drops FID 112903ExperimentalLubricant Eye Drops FID 112903 1 drop each eye one time
Receives: Other: Lubricant Eye Drops FID 112903
Optive Lubricant Eye DropsActive comparatorOptive Lubricant Eye Drops 1 drop each eye 1 time
Receives: Other: Optive Lubricant Eye Drops

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Drop Comfort Upon Instillation

    Drop comfort grading scale is a scale from 0 to 9, with 0 meaning most comfortable and 9 meaning most uncomfortable.

    Measured: Three minutes

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted7 May 2008 (estimated)
  2. Study startMay 2008
  3. Primary completionMay 2008
  4. Study completionMay 2008

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Crossover
Masking
Quadruple blind
Who is masked
Participant, Care provider, Investigator, Outcomes assessor
Enrolment
20 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT00673855
Sponsor's protocol ID
C-07-17
Status last verified
Jan 2012
First submitted
2 May 2008
Last updated
2 Feb 2012
Data monitoring committee
No

Questions about this trial

What is this clinical trial studying?

A study testing Lubricant Eye Drops FID 112903 and Optive Lubricant Eye Drops in people with Dry Eye, run by Alcon Research at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 2 Feb 2012. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Yes. Results are posted in the registry (first posted 10 Mar 2010). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Drop Comfort Upon Instillation (time frame: Three minutes). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 2 Feb 2012.

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