Clinical Evaluation of Fitting Investigational Contact Lenses
2018年5月24日 更新者：Johnson & Johnson Vision Care, Inc.
This study is a non-randomized, open label, bilateral, non- dispensing clinical trial with only one visit.
The Eye Care Providers will be provided with a fitting guide and will determine the initial study lens selection.
Each subject will wear either the investigational contact lenses or marketed contact lenses for approximately 30-90 minutes.
This study aims to evaluate the ECPs impression of the fitting guide for a novel multifocal lens and also their success in fitting the lenses.
調査の概要
研究の種類
介入
入学 (実際)
23
段階
- 適用できない
連絡先と場所
このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。
研究場所
-
-
Florida
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Jacksonville、Florida、アメリカ、32256
- Vistakon Research Clinic
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-
参加基準
研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。
適格基準
就学可能な年齢
40年～70年 (大人、高齢者)
健康ボランティアの受け入れ
はい
受講資格のある性別
全て
説明
Inclusion Criteria:
- The subject must read, understand, and sign the STATEMENT OF INFORMED CONSENT and receive a fully executed copy of the form
- The subject must appear able and willing to adhere to the instructions set forth in this clinical protocol.
- Healthy adult males or females that are at least 40 years of age and no more than 70 years of age.
- The subject must either be wearing a presbyopic contact lens correction (e.g., reading spectacles over contact lenses, multifocal or monovision contact lenses, etc.) or if not respond positively to at least one symptom on the "Presbyopic Symptoms Questionnaire".
- The subject is a current soft spherical or toric contact lens wearer (defined as a minimum of 6 hours of wear per day at least two days of the week for a minimum of 1 month prior to the study).
- The subject's distance spherical equivalent or spherical component (if fit with a toric lens) of their refraction must be in the range -1.25 D to -3.75 D in each eye.
- The subject's refractive cylinder must be 0.00 D to -1.50 D in at least one eye and no greater than -1.50 D in either eye.
- The subject's refractive cylinder axis must be 90°±30° or 180°±30° in each eye.
- The subject's ADD power must be in the range of +0.75 D to +2.50 D in each eye.
- The subject must have best corrected visual acuity of 20/20-3 or better in each eye.
- The subject must have a wearable pair of spectacles if required for their distance vision.
Exclusion Criteria:
- Ocular or systemic allergies or disease, or use of medication which might interfere with contact lens wear.
- Pregnancy or lactation.
- Currently diagnosed with diabetes.
- Infectious diseases (e.g. hepatitis, tuberculosis) or an immune-suppressive disease (e.g. HIV).
- Clinically significant (Grade 3 or 4) corneal edema, corneal vascularization, corneal staining, tarsal abnormalities or bulbar injection, or any other corneal or ocular abnormalities which would contraindicate contact lens wear.
- Entropion, ectropion, extrusions, chalazia, recurrent styes, dry eye, glaucoma, history of recurrent corneal erosions.
- Any previous, or planned, ocular or intraocular surgery (e.g., radial keratotomy, PRK, LASIK, lid procedures, cataract surgery, retinal surgery, etc.).
- A history of amblyopia, strabismus or binocular vision abnormality.
- Any ocular infection or inflammation.
- Any ocular abnormality that may interfere with contact lens wear.
- Use of any ocular medication, with the exception of rewetting drops.
- History of herpetic keratitis.
- Participation in any contact lens or lens care product clinical trial within 30 days prior to study enrollment.
- Employee of clinical site (e.g., Investigator, Coordinator, Technician)
研究計画
このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。
研究はどのように設計されていますか？
デザインの詳細
- 主な目的：処理
- 割り当て：非ランダム化
- 介入モデル：単一グループの割り当て
- マスキング：なし（オープンラベル）
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
実験的：etafilcon A Toric Multifocal
|
Subjects who are habitual contact lens wearers with Presbyopic correction or Presbyopic symptoms, at least 40 years of age and no more than 70 years of age, will be fitted, according to the fitting guides, with either the Multifocal Contact Lens or an Toric Multifocal Contact Lens if refractive cylinder power of the eye is between -1.00 to -1.50.
The Intervention is approximately 30-90 minutes of wear time during a 1-day visit.
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アクティブコンパレータ：etafilcon A Multifocal
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Subjects who are habitual contact lens wearers with Presbyopic correction or Presbyopic symptoms, at least 40 years of age and no more than 70 years of age, will be fitted, according to the fitting guides, with either the Multifocal Contact Lens or an Toric Multifocal Contact Lens if refractive cylinder power of the eye is between -1.00 to -1.50.
The Intervention is approximately 30-90 minutes of wear time during a 1-day visit.
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この研究は何を測定していますか？
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
The Average Number of Fitting Modifications to Optimize Vision
時間枠：15 minutes post lens insertion
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The eye care practitioner (ECP) followed the fitting guides to assess the vision provided by the study lenses and determined if a lens change (modification) was needed.
The ECP modified the lenses based upon the subject's responses in accordance with the fitting guide.
Up to two modifications per subject was allowed.
The number of modifications required by the ECP to optimize vision was reported.
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15 minutes post lens insertion
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二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Subject's Responses to Individual Item 1
時間枠：15 Minuted Post Lens Insertion
|
Subjects responses to individual item "Considering Your Experience With The Study Contact Lenses, Which Statement Best Describes Your Overall Satisfaction Of These Contact Lenses?".
This item had a response set of extremely satisfied, very satisfied, moderately satisfied, slightly satisfied and not at all satisfied.
The percentage of subject's in each response category was reported.
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15 Minuted Post Lens Insertion
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Subject's Responses to Individual Item 2
時間枠：15 Minuted Post Lens Insertion
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Subjects responses to individual item "Based On Your Experience Today, How Likely Are You To Purchase This Contact Lens?".
This item had a response set of extremely likely, very likely, somewhat likely, slightly likely and not at all likely.
The percentage of subject's in each response category was reported.
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15 Minuted Post Lens Insertion
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Subject's Responses to Individual Item 3
時間枠：15 Minuted Post Lens Insertion
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Subjects responses to individual item "Please Think About Your Experience Today With The Study Contact Lenses.
Please Indicate How You Satisfied You Are With The Overall Contact Lens Fitting Process?".
This item had a response set of very satisfied, satisfied, unsure, dissatisfied and very dissatisfied.
The percentage of subject's in each response category was reported.
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15 Minuted Post Lens Insertion
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Subject's Responses to Individual Item 4
時間枠：15 Minuted Post Lens Insertion
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Subjects responses to individual item "Where Would You Expect To Go Looking For Information About This Contact Lens?
Please Select All That Apply.".
The percentage of subject's in each response category was reported.
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15 Minuted Post Lens Insertion
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Subject's Responses to Individual Item 5
時間枠：15 Minuted Post Lens Insertion
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Subjects responses to individual item "If You Were To Purchase The Study Contact Lenses, With What Frequency Would You Expect To Wear Them?".
This item had a response set of All of the time, Usually, Frequently, Sometimes, Rarely and never.
The percentage of subject's in each response category was reported.
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15 Minuted Post Lens Insertion
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Subject's Responses to Individual Item 6
時間枠：15 Minuted Post Lens Insertion
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Subjects responses to individual item "What Are Your Current Vision Correction Solutions?".
The percentage of subject's in each response category was reported.
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15 Minuted Post Lens Insertion
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Subject's Responses to Individual Item 7
時間枠：15 Minuted Post Lens Insertion
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Subjects responses to individual item "Study Compare To Your Current Vision Correction Solutions?".
This item had a response set of Much better, somewhat better, about the same, somewhat worse and much worse.
The percentage of subject's in each response category was reported.
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15 Minuted Post Lens Insertion
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Subject's Responses to Individual Item 8
時間枠：15 Minuted Post Lens Insertion
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Subjects responses to individual item "Considering your experience with the study contact lens, how excited are you about this lens being available to purchase?".
This item had a response set of Very Excited, Excited, Unsure, Unexcited and Very Unexcited.
The percentage of subject's in each response category was reported.
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15 Minuted Post Lens Insertion
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Subject's Responses to Individual Item 9
時間枠：15 Minuted Post Lens Insertion
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Subjects responses to individual item "How would you rate your overall visual performance with the study contact lens?".
This item had a response set of Excellent, Very Good, Good, Fair and Poor.
The percentage of subject's in each response category was reported.
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15 Minuted Post Lens Insertion
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Subject's Responses to Individual Item 10
時間枠：15 Minuted Post Lens Insertion
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Subjects responses to individual item "Considering Your Experience With The Study Contact Lenses, Which Statement Best Describes Your Overall Opinion Of These Contact Lenses?".
This item had a response set of Excellent, Very Good, Good, Fair and Poor.
The percentage of subject's in each response category was reported.
|
15 Minuted Post Lens Insertion
|
協力者と研究者
ここでは、この調査に関係する人々や組織を見つけることができます。
研究記録日
これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。
主要日程の研究
研究開始 (実際)
2017年3月27日
一次修了 (実際)
2017年3月31日
研究の完了 (実際)
2017年3月31日
試験登録日
最初に提出
2017年4月17日
QC基準を満たした最初の提出物
2017年5月9日
最初の投稿 (実際)
2017年5月12日
学習記録の更新
投稿された最後の更新 (実際)
2018年6月29日
QC基準を満たした最後の更新が送信されました
2018年5月24日
最終確認日
2018年5月1日
詳しくは
この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。
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