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Pterygium clinical trials

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NCT ID: NCT06042296 Not yet recruiting - Pterygium Clinical Trials

Expression of CD44, PCNA and E-cadherin in Pterygium Tissue

Start date: October 2023
Phase:
Study type: Observational [Patient Registry]

Purpose: Pterygium is a common ocular surface disease defined by fibrovascular conjunctival growth extending onto the cornea. Its pathogenesis remains unclear. In severe cases, it may extend into the central cornea, inducing irregular corneal astigmatism and causing loss of vision. CD44( phagocytic glycoprotein-1 ) is involved in the organization of certain cellular processes, for instance, cell adhesion, division, and migration, by binding with its main ligand, hyaluronic acid. Proliferating cell nuclear antigen (PCNA) is a proliferation marker in the nucleus. E-cadherin is a calcium-dependent transmembrane glycoprotein that plays a significant role in the protection of tissue integrity and cell-to-cell adhesion. This study aimed to determine the role of CD44, proliferating cell nuclear antigen (PCNA), and E-cadherin in pterygium formation and recurrence.

NCT ID: NCT05812508 Not yet recruiting - Corneal Topography Clinical Trials

Comparison Between Bare Scleral Technique and Conjunctival Auto-graft on Corneal Topography After Pterygium Surgery

Start date: April 20, 2023
Phase:
Study type: Observational [Patient Registry]

Aim of the work: To study the corneal topographic pattern changes in patients who have pterygium excision by two surgical techniques (bare sclera, conjunctival autograft).

NCT ID: NCT04683159 Not yet recruiting - Pterygium Clinical Trials

Brimonidine Tartrate for Pterygium Surgery

Start date: February 2021
Phase: N/A
Study type: Interventional

Pterygium excision and conjunctival autograft surgery is commonly done to treat pterygiums. Excessive bleeding during the procedure creates a challenging operating field, prolongs surgery time, and prolongs healing. Brimonidine tartrate has a vasoconstrictive effect, which helps to reduce the amount of blood flow and hyperemia to the eye. Preoperative use of brimonidine has been shown to decrease subconjunctival hemorrhage during procedures such as cataract surgery, laser assisted in situ keratomileusis, strabismus surgery, and intravitreal injections. The focus of this study is to assess the effect of preoperative application of brimonidine tartrate 0.15% (Alphagan) and 0.025% (Lumify) on reducing hemorrhage during pterygium excision and conjunctival autograft surgery.

NCT ID: NCT04682054 Not yet recruiting - Glaucoma Clinical Trials

Molecular Taxonomy of Surgically-harvested Ocular Tissues Defined by Single-cell Transcriptomics

Eyesinglecell
Start date: January 15, 2021
Phase: N/A
Study type: Interventional

The surgically-harvested eye tissue (ie. vitreous-retinal proliferative membrane, outflow pathway, retinas, and pterygium) is a complex tissue responsible for maintaining intraocular homeostasis or mediating ocular pathogenesis. Dysfunction of one or more resident cell types within the tissues results in different ocular disorder, leading to vision loss, or even blindness. In this study, we aim to use single-cell RNA sequencing to generate a comprehensive cell atlas of surgically-harvested eye tissues.

NCT ID: NCT04400097 Not yet recruiting - Clinical trials for the Efficacy and Effect on Patient Comfort of a Hidden-knot Continuous Suture for Pterygium Excision With Conjunctival Autograft

The Influence of Suture Method in Conjunctival Autograft Transplantation on Postoperative Ocular Discomfort for Primary Pterygium

Start date: May 21, 2020
Phase: N/A
Study type: Interventional

To evaluate the efficacy and effect on patient comfort of a hidden-knot continuous suture for pterygium excision with conjunctival autograft,compared with two-knot continuous sutures and multi-knot interrupted sutures.

NCT ID: NCT04151862 Not yet recruiting - Pain, Postoperative Clinical Trials

The Two Most Common Ways Post-operative Eye Patch Are Therapeutic Contact Lenses (TCL) and Overnight Bandaging With Tight Bandage Patch: This Study is Designed to Determine the Most Effective Post-operative Care to Relief the Patient's Discomfort After Pterygium Excision Surgery

Start date: December 1, 2019
Phase: N/A
Study type: Interventional

This study is designed to determine the most effective post-operative care to relief the patient's discomfort after pterygium excision surgery.

NCT ID: NCT03314389 Not yet recruiting - Pterygium Clinical Trials

The Corneal and Conjunctiva Sensation Before and After Pterygium Surgeries

Start date: May 1, 2018
Phase: N/A
Study type: Interventional

The purpose of this current study is to examine the sensation of the corneal and conjunctiva sensation before and after pterygium surgeries by Cochet bonnet esthesiometer and to examine epidemiological, clinical and imaging factors the influence the sensation

NCT ID: NCT03304366 Not yet recruiting - Pterygium Clinical Trials

Corneal Changes With Pentacam Before and After Pterygium

Start date: November 2017
Phase: N/A
Study type: Observational

Aim of this study is to assess the corneal changes before and after pterygium excision by using pentacam system.

NCT ID: NCT03301974 Not yet recruiting - Pterygium Clinical Trials

A Comparison Between Surgical Techniques for Securing Conjunctival Autografting in Primary Pterygium Surgery

Start date: February 24, 2019
Phase: N/A
Study type: Interventional

Pterygium is a fibrovascular wing shaped encroachment of conjunctival fold on to the cornea with elastotic degeneration of a subconjunctival tissue, The standard treatment for pterygium is surgical excision, but the recurrence rate after surgery can be as high as 24%-89%, which compromises outcomes. Based on the simple excision of pterygium, multiple strategies and techniques have been developed to reduce the high rate of pterygium recurrence. The investigators aim was to compare the safety, efficacy, overall patient satisfaction and recurrence rate of suturing, fibrin gluing and sutureless glue-free technique for attaching conjunctival autograft in primary pterygium surgery.

NCT ID: NCT02782260 Not yet recruiting - Dry Eye Syndromes Clinical Trials

Assessment of the Efficacy of Ocular Dipyridamole in the Treatment of Dry Eye Symptomology in Subjects With Pterygium

Start date: July 2016
Phase: Phase 2
Study type: Interventional

Subjects with pterygium and associated dry eye symptoms (DES) are randomized into an active cohort (receiving ocular administration of Dipyridamole) or placebo cohort (ocular administration of vehicle). Monthly follow up is conducted for 12 months. Testing conducted at follow up will assess dry eye / pterygium symptoms and endpoints and review the efficacy of the intervention.