Other Clinical Trial - Evolution of a Novel Optical Coherence Tomography

Clinical Trial Summary

Comparison of corneal topography based on oct OCT principle (CASIA2) with Pentacam and Scheimpflug-based biomechanical devices (Corvis ST) in screening and diagnosing keratoconus; and evaluation of the consistency with Pentacam in measuring corneal parameters (such as curvature and thickness).

Interventional studies are often prospective and are specifically tailored to evaluate direct impacts of treatment or preventive measures on disease.

Observational studies are often retrospective and are used to assess potential causation in exposure-outcome relationships and therefore influence preventive methods.

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Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

NCT number	NCT06152484
Study type	Observational
Source	Tianjin Eye Hospital
Contact	Shuangcheng Li, Master
Phone	022-27313336-7539
Email	lscdoc@163.com
Status	Recruiting
Phase
Start date	July 1, 2023
Completion date	April 1, 2024

Evolution of a Novel Optical Coherence Tomography Based Index in Diagnosing Keratoconus

Clinical Trial Summary

Clinical Trial Description

Study Design

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