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Pterygium clinical trials

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NCT ID: NCT02866968 Completed - Pterygium Clinical Trials

Clinical Outcomes of Femtosecond Laser-assisted Pterygium Surgery (FLAPS)

FLAPS
Start date: July 6, 2016
Phase: N/A
Study type: Interventional

The study will be a pilot interventional case series aiming to treat 30 patients with Femtosecond Laser-assisted Pterygium Surgery (FLAPS). All patients included will undergo FLAPS in one eye. All procedures will be performed in SNEC by fully qualified surgeons. The doctor is informed of the procedure on the day of.

NCT ID: NCT02342392 Completed - Pterygium Clinical Trials

Intralesional Ranibizumab on Pterygium Vascularity, Size and Recurrence Rate: a Pilot Study

Start date: September 2012
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to evaluate the pterygium vascularity and size before and after intralesional ranibizumab injection and to evaluate its recurrence rate following pterygium excision surgery.

NCT ID: NCT02160769 Completed - Dry Eye Clinical Trials

Tear Layer Lipid Thickness in Pterygium Patient Before and After Surgery

Start date: November 2013
Phase:
Study type: Observational

The investigators study aims to capture the objective effects of pterygium surgery on tear layer lipid thickness and the tear layer. Previous objective studies of the tear film has been limited to corneal staining grading, tear break up time and Schirmer's test which have been shown to poor to moderate repeatability. The effect of pterygiums on tear layer lipid thickness (LLT) has not previously been explored. With the LipiView Ocular Surface Interferometer, the investigators have the ability to assess the optical coherence interference pattern produced by light reflected off the tear film in a safe and non-invasive manner. Software analysis of the image then measures the tear LLT which can be used to objectively quantify the diagnosis of lipid-deficient dry eye.

NCT ID: NCT02151305 Completed - Cataract Clinical Trials

Different Hemostasis According to the Anesthetic Agents

Start date: August 2010
Phase: N/A
Study type: Interventional

We investigated the hemostatic differences according to the main anesthetic agents by analyzing rotational thromboelastometry (ROTEM) under the hypothesis that propofol-based anesthesia would impair postoperative coagulability more than the sevoflurane-based anesthesia.

NCT ID: NCT02138019 Completed - Cataract Clinical Trials

The Application of Fibrin Glue (Tissucol Duo Quick) in External Eye Surgeries

Start date: December 2009
Phase: N/A
Study type: Interventional

The fibrin sealants are prepared from fibrinogen, thrombin, and sometimes factor XIII that have been purified from human plasma. Tissucol Duo Quick (Baxter, Vienna, Austria) is a kind of fibrin sealants with popular use. It is a 2-component tissue adhesive that resembles natural fibrin formation. This glue has 2 components: fibrinogen (mixed with factor XIII and aprotinin) and thrombin-CaCl2 solution. When equal amounts of the 2 components are mixed, the monomers aggregate by cross-linking, resulting in a fibrin clot. It forms a elastic, whitish substance and provides strong adhesion to the tissue. Therefore, it is a good agent to seal small wounds or to replace the use of suture.

NCT ID: NCT02059837 Completed - Recurrent Pterygium Clinical Trials

Clinical Analysis of Recurrence Patterns Following Conjunctival Autografts for Pterygium Surgery

Start date: February 2009
Phase: N/A
Study type: Observational

This study is conducted to evaluate its morphologic reproliferating patterns in patients with pterygium treated with the excision and conjunctival autograft.

NCT ID: NCT02009072 Completed - Pterygium Clinical Trials

Comparison Between Sutureless and Glue Free Versus Sutured Limbal Conjunctival Autograft in Primary Pterygium Surgery

Start date: April 2010
Phase: N/A
Study type: Interventional

Pterygium is a common ocular pathology facing ophthalmologists that has varied surgical management techniques and high rate of post-operative recurrence. The investigators aim was to compare and evaluate the safety and efficacy outcomes of those two surgical procedures in management of primary pterygium.

NCT ID: NCT02007174 Completed - Recurrent Pterygium Clinical Trials

Bevacizumab Injection for Recurrent Pterygium

Start date: March 2012
Phase: N/A
Study type: Observational

Blockade of vascular endothelial growth factor (VEGF) with bevacizumab has been used to treat abnormal vascular conditions of the anterior segment of the eye. In pterygium, anti-VEGF agents have been recently proposed as primary treatments, such as perioperative adjuvants, as well as treatments for pterygia recurrences after surgery. The aim of the present study was to prospectively evaluate the effect of three subconjunctival bevacizumab injections in patients with an early pterygium recurrence. Materials and Methods: The current study was a non-randomized single central trial. The method of ensuring allocation concealment was sequentially numbered. Patients with an early pterygium recurrence were selected and invited to participate in the study. Recurrence was defined as the presence of corneal vessels with concomitant conjunctival hyperemia within the first trimester after primary pterygium removal, and only patients with primary pterygium recurrence were included. Patient related factors such as pregnancy, women seeking to become pregnant, and lactating women were excluded from the study. All patients received three subconjunctival bevacizumab (2.5 mg/0.05 ml) injections (basal, 2 and 4 weeks) in the recurrence area of the pterygium, and were photographed at the third, sixth and twelfth months after the last bevacizumab injection. Photographic analyses were performed taking into account two pterygium areas: the first measure included only the vessel area in the corneal surface, while the second measure included, both, conjunctival and corneal vessel area (corneal-conjunctival area of hyperemia). Neovascularization area of each pterygium was determined using digital slit lam pictures, which were analyzed using Photoshop CS4, in order to get pixels measurements of the lesion.

NCT ID: NCT02002338 Completed - Pterygium Clinical Trials

Different Surgical Techniques for Pterygium Surgery

Start date: February 2013
Phase: N/A
Study type: Observational

A study to research the post-operative results according to the chosen surgical technique and evaluate the refractive changes before and after the excision of pterygium.

NCT ID: NCT01744756 Completed - Recurrent Pterygium Clinical Trials

Subconjunctival Bevacizumab and Recurrent Pterygium

BRP
Start date: February 2012
Phase: Phase 2/Phase 3
Study type: Interventional

A study to research whether subconjunctival bevacizumab injection may potentially suppress neovascularization in pterygium, retarding and decreasing the size of recurrent pterygium.