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Recurrent Pterygium clinical trials

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NCT ID: NCT05362253 Completed - Recurrent Pterygium Clinical Trials

Micro-Conjunctival Autografting Combined With Amniotic Membrane Transplantation Treating Recurrent Pterygium Trial

Start date: March 1, 2021
Phase: N/A
Study type: Interventional

To observe the effect of micro-conjunctival autografting combined with amniotic membrane transplantation on the postoperative recurrence, complications and ocular surface symptoms among patients with recurrent pterygium.

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: 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: 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.

NCT ID: NCT01319721 Completed - Recurrent Pterygium Clinical Trials

Recurrent Pterygium Surgery Using Mitomycin C With Limbal Conjunctival or Amniotic Membrane

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

To compare the outcomes of limbal conjunctival autograft (LCAG) versus amniotic membrane graft (AMG) when combined with intraoperative 0.02% mitomycin C (MMC) after pterygium removal in patients with recurrent pterygium.