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Cornea clinical trials

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NCT ID: NCT05759780 Recruiting - Skin Diseases Clinical Trials

OCT Vibrography for Biomechanical Properties of Tissues

Start date: August 19, 2023
Phase: N/A
Study type: Interventional

The overall goal of this study is to develop OCT Vibrography (aka OCT elastography) as a novel tool for measuring biomechanical properties of human tissues in vivo.

NCT ID: NCT05232539 Recruiting - Glaucoma Clinical Trials

Efficiency of Intraoperative Optical Coherence Tomography (iOCT)

Start date: May 2022
Phase: N/A
Study type: Interventional

Efficiency of Intraoperative Optical Coherence Tomography (iOCT) Hypothesis: The use of iOCT during surgery offers the advantage of a new view of the operating field, theoretically allows more precise performance and can also change decision-making mechanisms during surgery with more precise visual control of some surgical steps (incision adaptation, differentiation of healthy and pathological tissue, placement of the implant, graft, etc.) The disadvantage is the prolongation of the operation and thus the theoretical increase in possible complications related to the operation (bleeding, infection, patient subjective problems - pain, restlessness, poorer cooperation and the resulting other possible risks, such as unexpected patient movement). Aim: Determining the effectiveness of iOCT use in different types of eye surgery. Evaluation of advantages and disadvantages of using iOCT.

NCT ID: NCT05204329 Recruiting - Cornea Clinical Trials

Safety of Topical Mesenchymal Stromal Cell Secretome for Ocular Surface Disease

MSCSecretome
Start date: January 24, 2024
Phase: Early Phase 1
Study type: Interventional

This study is a longitudinal assessment using a classic dose-escalation study design to assess the safety and maximal tolerated dose (MTD) of topical MSC Secretome eye drops. The study will be conducted at Illinois Eye and Ear Infirmary located at University of Illinois at Chicago. The study will use anterior segment Optical Coherence Tomography (OCT)/Scheimpflug Imaging, esthesiometry, and visual analogue scale (VAS) to assess treatment tolerability.

NCT ID: NCT04626583 Recruiting - Safety Clinical Trials

Safety of Locally Delivered Allogeneic Mesenchymal Stromal Cells

Start date: March 5, 2021
Phase: Phase 1
Study type: Interventional

This study is a longitudinal assessment using a classic dose-escalation study design to assess the safety and maximal tolerated dose (MTD) of locally delivered allogeneic mesenchymal stromal cells (MSC) for promoting corneal repair. The study will be conducted at Illinois Eye and Ear Infirmary located at University of Illinois at Chicago. The study will use digital conjunctival and corneal photography and corneal Scheimpflug Imaging, densitometry, and pachymetry for assessment of safety and corneal wound healing.

NCT ID: NCT04439552 Recruiting - Pain, Postoperative Clinical Trials

fMRI and IVCM Cornea Microscopy of CXL in Keratoconus

Start date: October 4, 2021
Phase:
Study type: Observational

Evaluation of neuroplasticity of pain pathways and corneal afferent nerve regeneration following corneal crosslinking (CXL) in keratoconus patients using fMRI and corneal In Vivo Confocal Microscopy (IVCM).

NCT ID: NCT04323358 Recruiting - Surgery Clinical Trials

Agreement and Accuracy of Different Devices for Biometry Measurements in Patients With Cataract

Comparison
Start date: March 5, 2020
Phase: N/A
Study type: Interventional

The rationale of this study is to compare repeatability, reproducibility and agreement of three different AS-OCT devices and Pentacam. The investigational devices are approved biometry and keratometry devices to perform biometric/keratometric measurements preoperatively before cataract surgery. The measurements are used to calculate the needed IOL power. Measurements with all four devices will be performed 3 times consecutively by two trained observer. The order of the observer, the order of devices as well as the eye (left/right) is randomized. Examinations will be implemented in accordance with the approved investigational plan on subjects and includes: repeated biometry/keratometry with four different devices

NCT ID: NCT04066439 Recruiting - Cornea Clinical Trials

The Marker Expression of Corneal Surface From Penetrating Keratopathy After Collagenase A Assisted COMET Case Series

Start date: August 1, 2019
Phase:
Study type: Observational

In order to examine the cells of the corneal epithelium in the patients who receive corneal transplantation after collagenase A assisted cultivated oral mucosa epithelium transplant (CA-COMET), we analyzed the specimens from penetrating keratoplasty with immunochemical staining.

NCT ID: NCT03299530 Recruiting - Astigmatism Clinical Trials

Accuracy of Corneal Astigmatism in Different Region Modes

Start date: October 10, 2017
Phase:
Study type: Observational

To analyze the difference between measured total corneal astigmatism and actual corneal astigmatism under different region modes and optimize the region setting.

NCT ID: NCT03010748 Recruiting - Cornea Clinical Trials

Multi-center Clinical Trial on Corneal Morphology Analysis in Chinese Population

Start date: November 2015
Phase:
Study type: Observational

Based on the corneal morphometry instrumentation Oculus Pentacam, which is commonly used before and after clinical refractive surgery, we will collect the corneal morphological and biologic parameters of the population under refractive surgery screening in refractive surgery centers around the country, and construct corneal morphology database in different living areas of Chinese people. Based on this, compared with the suspected keratoconus and keratoconus population, the screening criteria and reference standards accord with the characteristics of keratoconus of Chinese ethnic will be achieved.

NCT ID: NCT02614625 Recruiting - Diabetes Clinical Trials

Spectral-domain Optical Coherence Tomography of the Eye

Start date: December 2014
Phase: N/A
Study type: Observational

An increasing number of clinical studies on SD-OCT of ocular pathologies and potential new clinical applications has recently been published in the peer-reviewed literature. However, the successful use of SD-OCT in routine clinical use depends upon the diagnostic sensitivity, biometric accuracy and reliability of the SD-OCT machines. This prospective, comparative, observational study aims to evaluate the imaging quality and diagnostic performance of two commercially available SD-OCT machines for both the anterior and posterior segment of the eye.