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Evaluation of Neovis® Total Multi Versus Systane® Balance on Ocular Dryness Associated With Meibomian Gland Dysfunction

3 januari 2022 uppdaterad av: Horus Pharma

Multicentric, Randomized, Comparative Clinical Study on the Evaluation of the Efficacy and Safety of Neovis® Total Multi Versus Systane® Balance on the Treatment of Ocular Dryness Associated With Meibomian Gland Dysfunction

This study is a multicentric, comparative, randomized, investigator-blinded, in parallel groups study to demonstrate the non-inferiority of Neovis® Total Multi in comparison with Systane® Balance, in terms of improvement of stability of Tear film in patients with eye dryness associated to meibomian gland dysfunction, after 28 days of treatment.

Studieöversikt

Status

Har inte rekryterat ännu

Studietyp

Interventionell

Inskrivning (Förväntat)

120

Fas

  • Inte tillämpbar

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studiekontakt

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 och äldre (Vuxen, Äldre vuxen)

Tar emot friska volontärer

Nej

Kön som är behöriga för studier

Allt

Beskrivning

Inclusion Criteria:

  • Presenting dry eye symptoms for at least 6 months.
  • OSDI (Ocular Surface Disease Index) ≥ 18
  • At least one eye eligible with:

    • sum of peripheral corneal and conjunctival staining ≥ 4 and ≤ 9 (Oxford 0-15 grading scheme) AND
    • sum of 3 measurements of Tear film Break-Up Time (TBUT) ≤ 15s
  • Meibomian Gland Dysfunction on at least one eye (same eye eligible) with a score of 1 or higher for meibum quality score (from 0: clear to 3: toothpaste/obstruction) and evidence of partial or whole missing Meibomian Glands.
  • Ability and willingness to apply eyelid hygiene during the whole study, including wash-out period.
  • Having given freely and expressly his/her informed consent.
  • Able to comply with the study requirements, as defined in the present CIP, at the Investigator's appreciation.
  • In France: subject being affiliated to a health social security system.
  • Female subjects of childbearing potential should use a medically accepted contraceptive regimen since at least 12 weeks before the beginning of the study, during all the study and at least 1 month after the study end.

Exclusion Criteria:

  • Pregnant or nursing woman or planning a pregnancy during the study.
  • Subject deprived of freedom by administrative or legal decision.
  • Subject in a social or health institution
  • Subject who is under guardianship or who is not able to express his/her consent.
  • Use of contact lenses in either eye during the study.
  • Far best-corrected visual acuity ≤ 1/10.
  • Subject with severe ocular dryness with one of these conditions:

    • Eyelid or blinking malfunction
    • Corneal disorders not related to dry eye syndrome
    • Ocular metaplasia
    • Filamentous keratitis
    • Corneal neovascularization
  • History of ocular traumatism, ocular infection or ocular inflammation within the last 3 months.
  • History of ocular allergy or ocular herpes within the last 12 months.
  • Subjects who underwent ocular surgery, including laser surgery, in either eye within the last 6 months.
  • Any troubles of the ocular surface not related to dry eye syndrome.
  • Use of the following ocular treatments: isotretinoïd, cyclosporine, tacrolimus, sirolimus, pimecrolimus during the month preceding the inclusion.
  • IOP > 21 mmHg
  • Uncontrolled systemic disease
  • Alcohol abuse
  • Psychiatric disorders
  • Cognitive impairment that could affect evaluation of preferences or inability to understand written patient information
  • Participation in other clinical studies in the last month
  • Hypersensitivity to one or more components of the study product
  • Dry eye due to systemic disease, concomitant medication, malign conditions or idiopathic causes
  • Punctual plugs during the past 3 months
  • Use of lipid-containing eye drops during the past 3 months
  • Use of other therapeutic ophthalmics during the past 3 months
  • Earlier participation at this clinical trial or the patient being an investigator or a member of the personnel involved at this clinical trial

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: Parallellt uppdrag
  • Maskning: Enda

Vapen och interventioner

Deltagargrupp / Arm
Intervention / Behandling
Experimentell: Undersökningsprodukt
1 drop in each eye, 4 times per day
Aktiv komparator: Komparator
1 drop in each eye, 4 times per day

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Tear-Film Break Up Time (TBUT)
Tidsram: 28 days
Evaluation of the non-inferiority of Neovis® Total Multi in comparison with Systane® Balance, in terms of TBUT improvement, on worse eye
28 days

Sekundära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Tear-Film Break Up Time (TBUT) (prestanda)
Tidsram: 84 dagar
Huvudförändring från baslinjen för Tear-Film Break Up Time (TBUT) i det sämre ögat och det kontralaterala ögat
84 dagar
Cornea and conjunctiva staining (Oxford score) (performance)
Tidsram: 28 days
Main change from baseline of cornea and conjunctiva staining (Oxford score) in the worse eye and contralateral eye
28 days
Hornhinna och bindhinna färgning (Oxford poäng) (prestanda)
Tidsram: 84 dagar
Huvudförändring från baslinjen för hornhinna och konjunktiva färgning (Oxford poäng) i det sämre ögat och kontralateralt öga
84 dagar
Meibomian gland expression (performance)
Tidsram: 28 days
Main change from baseline of meibomian gland expression score in the worse eye and contralateral eye
28 days
Meibomian gland expression (performance)
Tidsram: 84 days
Main change from baseline of meibomian gland expression score in the worse eye and contralateral eye
84 days
Meibum quality (performance)
Tidsram: 28 days
Main change from baseline of meibum quality score in the worse eye and contralateral eye
28 days
Meibum quality (performance)
Tidsram: 84 days
Main change from baseline of meibum quality score in the worse eye and contralateral eye
84 days
Meiboscopy (performance)
Tidsram: 28 days
Main change from baseline of the number of partially missing or dropout meibomian glands in the worse eye and contralateral eye
28 days
Meiboscopy (performance)
Tidsram: 84 days
Main change from baseline of the number of partially missing or dropout meibomian glands in the worse eye and contralateral eye
84 days
Eyelid margin abnormalities (performance)
Tidsram: 28 days
Main change from baseline of the eyelid margin abnormalities score in the worse eye and contralateral eye
28 days
Eyelid margin abnormalities (performance)
Tidsram: 84 days
Main change from baseline of the eyelid margin abnormalities score in the worse eye and contralateral eye
84 days
OSDI (questionnaire) (performance)
Tidsram: 28 days
Main change from baseline of OSDI (Ocular Surface Disease Index) in the worse eye and contralateral eye
28 days
OSDI (questionnaire) (performance)
Tidsram: 84 days
Main change from baseline of OSDI (Ocular Surface Disease Index) in the worse eye and contralateral eye
84 days
Global performance by the investigator (performance)
Tidsram: 28 days
Global performance assessment by the investigator using a 4-point scale (Unsatisfactory, Not very satisfactory, Satisfactory, Very satisfactory)
28 days
Global prestanda av utredaren (prestanda)
Tidsram: 84 dagar
Global prestationsbedömning av utredaren med hjälp av en 4-gradig skala (Otillfredsställande, Inte särskilt tillfredsställande, Tillfredsställande, Mycket tillfredsställande)
84 dagar
Global performance by the patient (performance)
Tidsram: 28 days
Global performance assessment by the patient using a 4-point scale (Unsatisfactory, Not very satisfactory, Satisfactory, Very satisfactory)
28 days
Global performance by the patient (performance)
Tidsram: 84 days
Global performance assessment by the patient using a 4-point scale (Unsatisfactory, Not very satisfactory, Satisfactory, Very satisfactory)
84 days
Global tolerance by the investigator (safety)
Tidsram: 28 days
Global tolerance assessment by the investigator using a 4-point scale (Unsatisfactory, Not very satisfactory, Satisfactory, Very satisfactory)
28 days
Global tolerance by the investigator (safety)
Tidsram: 84 days
Global tolerance assessment by the investigator using a 4-point scale (Unsatisfactory, Not very satisfactory, Satisfactory, Very satisfactory)
84 days
Global tolerance by the patient (safety)
Tidsram: 28 days
Global tolerance assessment by the patient using a 4-point scale (Unsatisfactory, Not very satisfactory, Satisfactory, Very satisfactory)
28 days
Global tolerance by the patient (safety)
Tidsram: 84 days
Global tolerance assessment by the patient using a 4-point scale (Unsatisfactory, Not very satisfactory, Satisfactory, Very satisfactory)
84 days
Intensity of ocular symptoms upon instillation (safety)
Tidsram: 28 days
Evaluation of intensity of ocular symptoms upon instillation on a scale from 0 (none) to 3 (severe)
28 days
Intensity of ocular symptoms upon instillation (safety)
Tidsram: 84 days
Evaluation of intensity of ocular symptoms upon instillation on a scale from 0 (none) to 3 (severe)
84 days
Duration of ocular symptoms upon instillation (safety)
Tidsram: 28 days
Evaluation of duration of ocular symptoms upon instillation in seconds/minutes/hours
28 days
Duration of ocular symptoms upon instillation (safety)
Tidsram: 84 days
Evaluation of duration of ocular symptoms upon instillation in seconds/minutes/hours
84 days
Frequency of ocular symptoms upon instillation (safety)
Tidsram: 28 days
Evaluation of frequency of ocular symptoms upon instillation on a scale from 1 (rarely) to 4 (very often)
28 days
Frequency of ocular symptoms upon instillation (safety)
Tidsram: 84 days
Evaluation of frequency of ocular symptoms upon instillation on a scale from 1 (rarely) to 4 (very often)
84 days
Number of Adverse Events
Tidsram: 84 days
Collection of ocular and systemic adverse events
84 days

Andra resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Non-Invasive Tear film Break-Up Time (NIBUT) (exploratory, optional)
Tidsram: 28 days
Main change from baseline of Non-Invasive Tear film Break-Up Time (NIBUT) in the worse eye and contralateral eye
28 days
Non-Invasive Tear film Break-Up Time (NIBUT) (exploratory, optional)
Tidsram: 84 days
Main change from baseline of Non-Invasive Tear film Break-Up Time (NIBUT) in the worse eye and contralateral eye
84 days
Lipid layer thickness (exploratory, optional)
Tidsram: 28 days
Main change from baseline of lipid layer thickness with interferometry methods in the worse eye and contralateral eye
28 days
Lipid layer thickness (exploratory, optional)
Tidsram: 84 days
Main change from baseline of lipid layer thickness with interferometry methods in the worse eye and contralateral eye
84 days
Functional visual acuity (exploratory, optional)
Tidsram: 28 days
Main change from baseline of functional visual acuity in the worse eye and contralateral eye
28 days
Functional visual acuity (exploratory, optional)
Tidsram: 84 days
Main change from baseline of functional visual acuity in the worse eye and contralateral eye
84 days
Super Oxyde Dismutase (SOD) dosage (exploratory, optional)
Tidsram: 84 days
Main change from baseline of SOD1 and SOD2 in the worse eye
84 days
Goblet cells analysis (exploratory, optional)
Tidsram: 84 days
Main change from baseline of Goblet cells in the worse eye
84 days

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Sponsor

Utredare

  • Huvudutredare: Hoffart Louis, Vision Sud

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 (Förväntat)

1 januari 2022

Primärt slutförande (Förväntat)

1 oktober 2022

Avslutad studie (Förväntat)

1 december 2022

Studieregistreringsdatum

Först inskickad

10 december 2021

Först inskickad som uppfyllde QC-kriterierna

3 januari 2022

Första postat (Faktisk)

13 januari 2022

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)

13 januari 2022

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

3 januari 2022

Senast verifierad

1 januari 2022

Mer information

Termer relaterade till denna studie

Andra studie-ID-nummer

  • 21E1007

Plan för individuella deltagardata (IPD)

Planerar du att dela individuella deltagardata (IPD)?

Obeslutsam

IPD-planbeskrivning

Depending on any journal publication of the results

Läkemedels- och apparatinformation, studiedokument

Studerar en amerikansk FDA-reglerad läkemedelsprodukt

Nej

Studerar en amerikansk FDA-reglerad produktprodukt

Nej

produkt tillverkad i och exporterad från U.S.A.

Nej

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