- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT01961089
Galilei Lens Professional vs. Predicate Devices: a Comparison Study
GALILEI Lens Professional vs. Predicate Devices: a Comparison Study
연구 개요
상세 설명
Background: An accessory to the commercially available GALILEI Dual-Scheimpflug Corneal Topographer/Keratometer with the name "EBR Accessory" was developed by the company Ziemer Ophthalmic Systems AG for the measurement of intraocular distances. The combination is called "GALILEI Lens Professional". The measurement principle is based on on short coherence interferometry/-reflectometry, which has gained wide-spread application and has been applied clinically, including one of the members of this study group, for the precise measurement of axial, intraocular distances (12.1.). Such EBR Accessory measurements, in combination with measurements by the GALILEI, may be applied to given intra-ocular lens (IOL) types and IOL equations, an permit the calculation of suggested IOLs that are implanted during cataract surgery, in order to achieve the desired vision correction. To register this accessory for sale, the precision and agreement to existing devices with similar applications ("predicate devices") must be demonstrated. One complete measurement consists of a cornea-topography/keratometry scan, followed immediately by three consecutive, axial biometry scans of the anterior segment (cornea and crystalline lens) and - after a short re-alignment - three consecutive, axial biometry scans of the retina. The measurement process is continuous, but divided in two steps. Blinking by the patient is possible in between the two steps, which increases patient comfort and, in certain cases, measurement success. Precision is evaluated by three repeated, complete measurements with the GALILEI Lens Professional and each predicate device. Two standard devices with comparable optical technology that are used in routine cataract surgery were declared as predicate devices. These two devise are typically used in combination with standard keratometers, as which the GALILEI Lens Professional may be employed as well.
Goal: The comparison of the GALILEI Lens Professional to predicate devices with respect to precision in measuring postoperative, calculated target refractions in cataract patients, and versatility of measurable quantities.
연구 유형
등록 (실제)
단계
- 해당 없음
연락처 및 위치
연구 장소
-
-
Aargau
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Reinach, Aargau, 스위스, 5734
- Eye Clinic Orasis
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참여기준
자격 기준
공부할 수 있는 나이
건강한 자원 봉사자를 받아들입니다
연구 대상 성별
설명
Inclusion Criteria:
- spherical equivalent between -10 D and +10 D
- best-corrected VA of 20/100 or better.
Exclusion Criteria:
- strabism
- blepharitis
- nystagmus
- amblyopia
- anisometropia (spherical equivalent > 1D)
- angle closure glaucoma
- seizure disorder
- brain damages
- Down syndrome
- trisomy 13 or 18
- cerebral palsy
- other serious disorders of the eye or central nervous systems
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 특수 증상
- 할당: 무작위화되지 않음
- 중재 모델: 단일 그룹 할당
- 마스킹: 하나의
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
|
실험적: Normal
Arm: Normal eyes Interventions: Galilei Lens Professional, IOLMaster, Lenstar
|
Measurement device
Measurement device
Measurement device
|
|
활성 비교기: Mild Cataract
Arm: Eyes with mild cataract Interventions: Galilei Lens Professional, IOLMaster, Lenstar
|
Measurement device
Measurement device
Measurement device
|
|
실험적: Severe cataract
Arm: Eyes with severe cataract Interventions: Galilei Lens Professional, IOLMaster, Lenstar
|
Measurement device
Measurement device
Measurement device
|
연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Agreement With Predicate Devices in Terms of Agreement 1
기간: 3 months
|
Assessed parameters: Axial Length (AL; G6, IOLM, LS) Central Corneal Thickness (CCT; G6, LS)) Anterior Chamber Depth (ACD; G6, IOLM, LS) Lens Thickness (LT; G6, LS) Corneal Curvature (SimK; G6, IOLM, LS) White-to-White (WtW; G6, IOL, LS) |
3 months
|
|
Agreement With Predicate Devices in Terms of Agreement 2
기간: 3 months
|
Assessed Parameters: Simulated Corneal Curvature (SimK; G6, IOLM, LS) |
3 months
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2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Agreement With Devices of the Same Type in Terms of Repeatability
기간: 3 months
|
Assessed parameters: Axial Length (AL) Central Corneal Thickness (CCT) Anterior Chamber Depth (ACD) Lens Thickness (LT) Corneal Curvature (SimK) White-to-White (WtW) |
3 months
|
공동 작업자 및 조사자
수사관
- 수석 연구원: Bojan Pajic, MD, Eye Clinic Orasis
연구 기록 날짜
연구 주요 날짜
연구 시작
기본 완료 (실제)
연구 완료 (실제)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (추정)
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .