- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT02024698
Multi-center Clinical Evaluation of PC 1-Day vs 1-Day Acuvue Moist
19 juli 2020 uppdaterad av: CooperVision, Inc.
The objective of this study is to compare the clinical performance of ProClear 1-Day versus 1-Day Acuvue Moist each for one week of daily disposable wear.
Studieöversikt
Detaljerad beskrivning
The purpose of this cross-over study is to evaluate the clinical performance of the ProClear-1 Day in comparison with 1-Day Acuvue® Moist®.
In particular, the study will focus on lens wearing comfort.
Studietyp
Interventionell
Inskrivning (Faktisk)
43
Fas
- Inte tillämpbar
Kontakter och platser
Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.
Studieorter
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Arizona
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Phoenix, Arizona, Förenta staterna, 85032
- Phoenix Eye Care, PLLC
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Illinois
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Lake Zurich, Illinois, Förenta staterna, 60047
- Lake Zurich Eye Care
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Ohio
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Athens, Ohio, Förenta staterna, 45701
- Drs. Quinn, Foster & Assoc.
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New Albany, Ohio, Förenta staterna, 43054
- Vision Professionals
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-
Deltagandekriterier
Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.
Urvalskriterier
Åldrar som är berättigade till studier
18 år till 40 år (Vuxen)
Tar emot friska volontärer
Nej
Kön som är behöriga för studier
Allt
Beskrivning
Inclusion Criteria:
A person is eligible for inclusion in the study if he/she:
- Is between 18 and 40 years of age (inclusive)
- Have the use of a mobile phone to send and receive text messages throughout the day for the duration of the study.
- Has had a self-reported visual exam in the last two years
- Is an adapted soft CL (Contact Lens) wearer
- Must be able to wear their lenses at least 6 full days over the 7 days; 14 hours per day, assuming there are no contraindications for doing so
- Has a CL spherical prescription between - 1.00 and - 6.00 (inclusive)
- Has less than 0.75D (Diopters) spectacle cylinder in each eye.
- Is correctable to a visual acuity of 20/25 or better in both eyes
- Has clear corneas and no active ocular disease
- Has read, understood and signed the information consent letter.
- Is willing to comply with the wear schedule (at least 40 hrs per week)
- Is willing to comply with the visit schedule
Exclusion Criteria:
A person will be excluded from the study if he/she:
- Has never worn contact lenses before.
- Currently wears rigid gas permeable contact lenses.
- Has a history of not achieving comfortable CL wear (5 days per week; > 8 hours/day)
- Has a CL prescription outside the range of - 1.00 to -6.00D
- Has a spectacle cylinder greater than -0.50D of cylinder in either eye.
- Has best corrected spectacle distance vision worse then 20/25 in either eye.
- Has any systemic disease affecting ocular health.
- Is using any systemic or topical medications that will affect ocular health.
- Has any ocular pathology or severe insufficiency of lacrimal secretion
- Has persistent, clinically significant corneal or conjunctival staining
- Has active neovascularization or any central corneal scars.
- Is aphakic.
- Is presbyopic.
- Has undergone corneal refractive surgery.
- Is participating in any other type of eye related clinical or research study.
Studieplan
Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Behandling
- Tilldelning: Randomiserad
- Interventionsmodell: Crossover tilldelning
- Maskning: Enda
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
|---|---|
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Aktiv komparator: omafilcon A
Study participants are randomized to wear omafilcon A lenses.
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kontaktlins
Andra namn:
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Aktiv komparator: etafilcon A
Study participants are randomized to wear etafilcon A lenses.
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kontaktlins
Andra namn:
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Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
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Comfort (Subjective Assessment)
Tidsram: Baseline
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Subjective Assessment of comfort on insertion at baseline for each pair using questionnaire and rated on subjective response scale.
(0-10; 0= very uncomfortable, 10=cannot feel)
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Baseline
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Comfort (Subjective Assessment)
Tidsram: 1 Week
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Subjective Assessment: Insertion Comfort, Comfort During Day, Comfort Prior to Removal, Comfort Overall for each pair using questionnaire and rated on subjective response scale.
(0-10; 0= very uncomfortable, 10=cannot feel)
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1 Week
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Hydration (Subjective Assessment)
Tidsram: Baseline
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Subjective Assessment of hydration on insertion at baseline for each pair using questionnaire and rated on subjective response scale.
(0-10; 0= very dehydrated, not hydrophilic, very dry, 10=very hydrated, ultra hydrophilic)
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Baseline
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Hydration (Subjective Assessment)
Tidsram: 1 Week
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Subjective Assessment: Initial Hydration, Hydration During Day, Hydration Prior to Removal for each pair using questionnaire and rated on subjective response scale.
(0-10; 0= very dehydrated, not hydrophilic, very dry, 10=very hydrated, ultra hydrophilic)
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1 Week
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Vision Quality (Subjective Assessment)
Tidsram: Baseline
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Subjective Assessment: Visual quality on insertion at baseline for each pair using questionnaire and rated on subjective response scale (0-10; 0= clear vision, 10=perfectly sharp)
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Baseline
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Vision Satisfaction (Subjective Assessment)
Tidsram: 1 Week
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Subjective Assessment: Vision Satisfaction for each pair using questionnaire and rated on subjective response scale.
(0-10; 0= very unsatisfied, 10=very satisfied)
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1 Week
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Dryness (Subjective Assessment)
Tidsram: 1 Week
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Subjective Assessment: Dryness During Day, Dryness Prior to Removal, Overall Dryness for each pair using questionnaire and rated on subjective response scale.
(0-10; 0= very dry, 10=no dryness)
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1 Week
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Handling (Subjective Assessment)
Tidsram: 1 Week
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Subjective Assessment: Handling on Insertion and Removal, Overall Handling for each pair using questionnaire and rated on subjective response scale.
(0-10; 0= very difficult, 10=very easy)
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1 Week
|
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Eye Whiteness/Redness (Subjective Assessment)
Tidsram: 1 Week
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Subjective Assessment: Eye Whiteness/Redness for each pair using questionnaire and rated on subjective response scale.
(0-10; 0= significant redness, 10=totally white)
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1 Week
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Overall Sensation of Smoothness (Subjective Assessment)
Tidsram: 1 Week
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Subjective Assessment: Overall sensation of smoothness at 1 week wear for each pair when asked "How would you rate the overall sensation of smoothness (deposit resistance) of the first study lenses, over the last week of wear?" (Likert 1-5; 1=excellent, 2=good, 3=average, 4=below average, 5=poor)
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1 Week
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Overall Satisfaction for Lens
Tidsram: 1 Week
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Subjective Assessment: Satisfaction overall at 1 Week wear for each pair when asked "Overall, how satisfied was the subject with the study lenses, during the last week, with regards to: Overall?" (Likert 1-4; 1=completely satisfied, 2=somewhat satisfied, 3=somewhat dissatisfied, 4=completely dissatisfied)
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1 Week
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Samarbetspartners och utredare
Det är här du hittar personer och organisationer som är involverade i denna studie.
Sponsor
Utredare
- Huvudutredare: Donald Siegel, OD, Sun City West Eye Care
Studieavstämningsdatum
Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.
Studera stora datum
Studiestart
1 januari 2014
Primärt slutförande (Faktisk)
1 januari 2014
Avslutad studie (Faktisk)
1 mars 2014
Studieregistreringsdatum
Först inskickad
27 december 2013
Först inskickad som uppfyllde QC-kriterierna
27 december 2013
Första postat (Uppskatta)
31 december 2013
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
30 juli 2020
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
19 juli 2020
Senast verifierad
1 juli 2020
Mer information
Termer relaterade till denna studie
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- EX-MKTG-43
Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .