- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT01699750
Comparative In-Vivo Wetting Characteristics of Silicone Hydrogel Materials With Selected Lens Care Systems
3. desember 2014 oppdatert av: Alcon Research
The purpose of this study is to evaluate the lipid uptake, wetting characteristics, and visual performance of AIR OPTIX® AQUA and ACUVUE® OASYS® with HYDRACLEAR® contact lenses when used in conjunction with two contact lens care systems.
Studieoversikt
Status
Fullført
Forhold
Detaljert beskrivelse
This study will be divided into two phases.
In the Pre-Investigational Phase (Phase 1), participants will wear PureVision contact lenses for 30 days and use ReNu® Multiplus® for contact lens care.
Eligible participants will continue into the Investigational Phase (Phase 2) and be randomly assigned to wear AIR OPTIX® AQUA contact lenses or ACUVUE® OASYS® with HYDRACLEAR® contact lenses for a total of two months.
For contact lens care, participants will use OPTI-FREE® PUREMOIST® MPDS and BIOTRUE® for 30 days each.
Studietype
Intervensjonell
Registrering (Faktiske)
109
Fase
- Ikke aktuelt
Kontakter og plasseringer
Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.
Studiesteder
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Texas
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Fort Worth, Texas, Forente stater, 76134
- Contact Alcon Call Center at 1-888-451-3937 for Trial Locations
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Deltakelseskriterier
Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
18 år og eldre (Voksen, Eldre voksen)
Tar imot friske frivillige
Nei
Kjønn som er kvalifisert for studier
Alle
Beskrivelse
Inclusion Criteria:
- Read and understand the Participant Information Sheet;
- Read, sign, and date the Informed Consent;
- Be a current silicone hydrogel contact lens wearer using the contact lenses under a frequent replacement (bi-weekly or monthly) daily wear modality;
- Be classified as symptomatic and a depositor at the end of the replacement period according to protocol-specified criteria;
- Agree to wear study contact lenses as directed for the duration of the study and maintain the appointment schedule;
- Best corrected visual acuity of 6/9 or better in each eye;
- Normal eyes with the exception of the need for visual correction;
- Other protocol-defined inclusion criteria may apply.
Exclusion Criteria:
- Known sensitivity or intolerance to any of the contact lenses or contact lens care products to be used;
- Monocular vision (only one eye with functional vision or only one eye fitted with contact lenses);
- Use of systemic medication which might interfere with contact lens wear or produce dry eye side effects;
- Systemic disease which might interfere with contact lens wear or produce dry eye side effects;
- Systemic or ocular allergies which might interfere with contact lens wear;
- Ocular disease which might interfere with contact lens wear;
- Active ocular infection;
- Use of any concomitant topical ocular medications during the study period;
- Previous ocular surgery;
- Pregnant, planning to become pregnant, or lactating at the time of enrollment;
- Participation in an investigational drug or device study within 30 days of entering this study;
- Other protocol-defined exclusion criteria may apply.
Studieplan
Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.
Hvordan er studiet utformet?
Designdetaljer
- Tildeling: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Enkelt
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
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Eksperimentell: Air Optix Aqua
Lotrafilcon B contact lenses with OFPM and BIOTRUE for 30 days each
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Silicone hydrogel contact lenses, Phase 2
Andre navn:
Contact lens care system, Phase 2
Andre navn:
Contact lens care system, Phase 2
Silicone hydrogel contact lenses worn for 30 days, Phase 1
Andre navn:
Contact lens care system used for 30 days, Phase 1
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Aktiv komparator: Acuvue Oasys
Senofilcon A contact lenses with OFPM and BIOTRUE for 30 days each
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Contact lens care system, Phase 2
Andre navn:
Contact lens care system, Phase 2
Silicone hydrogel contact lenses worn for 30 days, Phase 1
Andre navn:
Contact lens care system used for 30 days, Phase 1
Silicone hydrogel contact lenses, Phase 2
Andre navn:
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Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
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Mean Ex-Vivo Total Lipid Uptake Per Lens
Tidsramme: Day 30
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The contact lens was aseptically removed from the eye.
Lipids were extracted and analyzed using a proprietary High Performance Liquid Chromatography technique.
A lower value indicates a cleaner lens surface.
One eye (study eye) contributed to the mean.
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Day 30
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Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
---|---|---|
Mean Non-Invasive Pre-Lens Tear Film Break Up Time (NIBUT)
Tidsramme: Day 30
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The pre-lens tear film is the layer of tears located on top of the contact lens between the eyelid and the contact lens.
NIBUT (i.e., the time elapsed between eye opening after a blink and the appearance of the first dark spot within the tear film) was measured using a diffuse illumination source (Tearscope) and videotography.
A longer NIBUT indicates a more stable tear film and greater on-eye lens wettability.
One eye (study eye) contributed to the mean.
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Day 30
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LogMAR Time-Controlled Visual Acuity (TCVA)
Tidsramme: Day 30
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Visual performance was measured binocularly (both eyes together) at two contrast levels using a validated Time Controlled Visual Acuity test (TCVA).
TCVA was recorded in VA units (1 VA unit=1 VA line=0.1 logMAR), with positive (+) values corresponding with VA better than 20/20 and negative (-) values worse than 20/20.
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Day 30
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Overall Comfort Measured With Visual Analog Scale (VAS)
Tidsramme: Day 30
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The participant rated overall comfort on a 100-millimeter analog scale by marking a line that best corresponds to their eye comfort (0=very poor, 100=excellent).
Both eyes were rated together as a single, retrospective evaluation of the previous 3 days of wear.
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Day 30
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Overall Dryness Measured With Visual Analog Scale (VAS)
Tidsramme: Day 30
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The participant rated overall dryness on a 100-millimeter analog scale by marking a line that best describes how dry their eyes feel (0=not at all dry, 100=very dry).
Both eyes were rated together as a single, retrospective evaluation of the previous 3 days of wear.
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Day 30
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Average Exposure Speed
Tidsramme: Day 30
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Exposure speed (rate of increase in exposed lens surface % (areas not protected by tear film) after the first tear film break and before the second blink) was measured with a diffuse illumination source (Tearscope) and videotography.
Higher speeds indicate worse tear film dynamics.
One eye (study eye) contributed to the mean.
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Day 30
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Minimum Protected Area
Tidsramme: Day 30
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Minimum protected area (i.e., minimum area of the lens (%) covered by the tear film during the interblink period) was measured using a diffuse illumination source (Tearscope) and videotography.
A higher value indicates a larger area of the tearfilm spread evenly over the lens (i.e., less area of tear film breakage).
One eye (study eye) contributed to the mean.
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Day 30
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Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Sponsor
Studierekorddatoer
Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.
Studer hoveddatoer
Studiestart
1. desember 2012
Primær fullføring (Faktiske)
1. november 2013
Studiet fullført (Faktiske)
1. november 2013
Datoer for studieregistrering
Først innsendt
2. oktober 2012
Først innsendt som oppfylte QC-kriteriene
2. oktober 2012
Først lagt ut (Anslag)
4. oktober 2012
Oppdateringer av studieposter
Sist oppdatering lagt ut (Anslag)
8. desember 2014
Siste oppdatering sendt inn som oppfylte QC-kriteriene
3. desember 2014
Sist bekreftet
1. desember 2014
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- M-12-043 / ID11-59
Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .
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