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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03923101
Other study ID # HKC
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date January 1, 2011
Est. completion date January 1, 2032

Study information

Verified date November 2023
Source Universität des Saarlandes
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

Aim of this study is to conduct longitudinal and cross-sectional analyses about the corneal ectatic disease Keratoconus based on data obtained from Keratoconus patients in the Homburg Keratoconus Center (HKC). The Homburg Keratoconus Center (HKC) was founded in 2010 and, up to now, comprises more than 2.000 Keratoconus patients. Topographic, tomographic and biomechanic characteristics of the disease are being analyzed with the intention to elucidate how the disease begins and develops during lifetime.


Recruitment information / eligibility

Status Recruiting
Enrollment 1200
Est. completion date January 1, 2032
Est. primary completion date January 1, 2028
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - All Keratoconus patients presenting in the department of ophthalmology, Saarland University Medical Center, Homburg, Saarland, Germany. Exclusion Criteria: - Patients without Keratoconus.

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
Topographic, tomographic and biomechanical analysis.
The study is based upon data obtained during routine medical follow-ups using the Pentacam high resolution (Oculus, Wetzlar, Germany) the Corvis ST (Oculus, Wetzlar, Germany) the Anterior-Segment Optical Coherence Tomograph (AS-OCT) Casia 2 (Tomey, Nagoya, Japan) the Ocular Response Analyzer (Reichert Technologies, New York, USA).

Locations

Country Name City State
Germany Department of Ophthalmology Homburg Saarland

Sponsors (1)

Lead Sponsor Collaborator
Universität des Saarlandes

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary An overview about development of anterior corneal curvature in Keratoconus disease during lifetime. The anterior radius of curvature (ARC, 3mm zone) of Keratoconus patients as measured by the Pentacam high resolution (Oculus, Wetzlar, Germany) at different ages (according to: Belin MW and Duncan JK. Keratoconus: The ABCD grading system. Klin Monbl Augenheilkd. 2016; 233(6): 701-707) is put into relation to the age of the Keratoconus patients. 01/01/2011-01/01/2019
Primary An overview about development of posterior corneal curvature in Keratoconus disease during lifetime. The posterior radius of curvature (PRC, 3mm zone) of Keratoconus patients as measured by the Pentacam high resolution (Oculus, Wetzlar, Germany) at different ages (according to: Belin MW and Duncan JK. Keratoconus: The ABCD grading system. Klin Monbl Augenheilkd. 2016; 233(6): 701-707) is put into relation to the age of the Keratoconus patients. 01/01/2011-01/01/2019
Primary An overview about development of the thinnest corneal pachymetry in Keratoconus disease during lifetime. The thinnest corneal pachymetry of Keratoconus patients as measured by the Pentacam high resolution (Oculus, Wetzlar, Germany) at different ages (according to: Belin MW and Duncan JK. Keratoconus: The ABCD grading system. Klin Monbl Augenheilkd. 2016; 233(6): 701-707) is put into relation to the age of the Keratoconus patients. 01/01/2011-01/01/2019
Primary An overview about development of the best corrected distance visual acuity in Keratoconus disease during lifetime. The best corrected distance visual acuity of Keratoconus patients as raised as part of the clinical examination at different ages (according to: Belin MW and Duncan JK. Keratoconus: The ABCD grading system. Klin Monbl Augenheilkd. 2016; 233(6): 701-707) is put into relation to the age of the Keratoconus patients. 01/01/2011-01/01/2019
Primary Reproducibility study: Kmax. Measurements of Kmax measured by different devices (Pentacam high resolution, Oculus, Wetzlar, Germany; Anterior-Segment Optical Coherence Tomograph (AS-OCT) Casia 2, Tomey, Nagoya, Japan) are being compared and set into relation at different Keratoconus stages with the intention to investigate, whether measurement inaccuracies occur at later Keratoconus stages using different devices. 01/01/2011-01/01/2019
Primary Reproducibility study: Thinnest corneal pachymetry. Measurements of the thinnest corneal pachymetry as measured by different devices (Pentacam high resolution, Oculus, Wetzlar, Germany; Anterior-Segment Optical Coherence Tomograph (AS-OCT) Casia 2, Tomey, Nagoya, Japan) are being compared and set into relation at different Keratoconus stages with the intention to investigate, whether measurement inaccuracies occur at later Keratoconus stages using different devices. 01/01/2011-01/01/2019
Primary Reproducibility study: Thinnest corneal pachymetry at the apex position. Measurements of the thinnest corneal pachymetry at the apex position as measured by different devices (Pentacam high resolution, Oculus, Wetzlar, Germany; Anterior-Segment Optical Coherence Tomograph (AS-OCT) Casia 2, Tomey, Nagoya, Japan) are being compared and set into relation at different Keratoconus stages with the intention to investigate, whether measurement inaccuracies occur at later Keratoconus stages using different devices. 01/01/2011-01/01/2019
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