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Evaluation of Tranilast to Treat Pterygium Before Excision (TPS)

Primary Purpose

Pterygium

Status
Completed
Phase
Phase 3
Locations
Brazil
Study Type
Interventional
Intervention
Tranilast, and Tissucol
Beriplast P
Sponsored by
Gildasio Castello de Almeida Junior
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Pterygium focused on measuring Tranilast, fibrin glue, primary pterygium, conjunctival autograft

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Primary pterygium

Exclusion Criteria:

  • Keratoconjunctivitis sicca
  • Sjögren disease
  • Vernal keratoconjunctivitis
  • Acne rosacea
  • Neurotrophic keratopathy
  • Severe dysfunction of the meibomius glands
  • Use of any immunosuppressive drug, through systemic and topical route
  • Aged under 18 years of age and vulnerable groups
  • Glaucoma and use of ocular hipotensor

Sites / Locations

  • Hospital de Base/FAMERP

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Tranilast

Control

Arm Description

CAT with FG and Tranilast and MMC 0.02%

CAT with FG and MMC 0.02%

Outcomes

Primary Outcome Measures

Recurrence rate at months six and twelve months Immunohistochemical and cell morphology analysis at the end of study, 12 months

Secondary Outcome Measures

Patient discomfort at day one, six and twelve months Safety of Tranilast

Full Information

First Posted
October 28, 2009
Last Updated
April 16, 2012
Sponsor
Gildasio Castello de Almeida Junior
Collaborators
Hospital de Base
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1. Study Identification

Unique Protocol Identification Number
NCT01003613
Brief Title
Evaluation of Tranilast to Treat Pterygium Before Excision
Acronym
TPS
Official Title
Evaluation of Tranilast as Adjunctive Therapy Before Primary Pterygium Excision Compared With Conjunctival Autograft
Study Type
Interventional

2. Study Status

Record Verification Date
March 2012
Overall Recruitment Status
Completed
Study Start Date
February 2009 (undefined)
Primary Completion Date
July 2011 (Actual)
Study Completion Date
March 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Gildasio Castello de Almeida Junior
Collaborators
Hospital de Base

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Recurrent or secondary pterygium often has often a growing fibrovascular tissue more exuberant than the primary. Histological findings differ from the primary, since the typical changes in the degenerate connective tissue are absent. The strong immunoreactivity and release of basic fibroblast growth (b-FGF) in cultured fibroblasts of recurrent pterygia suggest that fibroblasts may play an important role in pterygium recurrence. Tranilast used is an antiallergic drug that has an inhibitory effect on the release of chemical transmitters, such as histamine and leukotrienes from mast cells as well as a suppressive effect on vascular permeability.This drug also reduces TGF-β1 production and collagen synthesis in various cells. Tranilast might reduce pterygium recurrence by suppressing TGF-β1 synthesis in conjunctival fibroblast after pterygium surgery. The investigators want to confirm these findings and also compare the recurrence rate between the two types of surgery. Tranilast might be an alternative of mitomycin use, and also less toxic. This study aim to compare the effectiveness of preventing recurrence by using tranilast by topical subconjunctival administration previous to conjunctival autograft transplantation surgery in cases of primary pterygium, and will be perform clinical evaluation and TGF-beta-1 immunohistochemical detection by the anti-TGF-beta 1 antibody as well as fibroblast culture.
Detailed Description
This is a prospective, randomised, control trial of 50 participants. Twenty five patients in each arm. Twenty five patients undergo standard pterygium excision with the fibrin glue (Tissucol) conjunctival autograft . Twenty five patients undergo pterygium surgery with fibrin glue (Tissucol), and subconjunctival injection of 0.1 ml of Tranilast 1.0% in the head of pterygium 30 days before surgery. Participants will be reviewed, selected, and consented on a pre-assessment day. Surgery will be performed 4 at a time on an all day surgery operating list. Randomisation of the surgery type will be done at the time of surgery after the pterygium has been excised and the autograft taken. The surgeries will perform by a single surgeon (Almeida Jr, GC). Follow-up will occur at week 1,4, 26, 52. Slit lamp examination will indicate pterygium recurrence. Corneal recurrence will consider when it 0.5 mm of invaded conjunctival tissue,in the clear cornea from the anatomical limbus. The conjunctival recurrence will consider of any size conjunctive fibrovascular invasion inside the graft. The localization and of immunohistochemical will be perform for TGF-B.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pterygium
Keywords
Tranilast, fibrin glue, primary pterygium, conjunctival autograft

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
32 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Tranilast
Arm Type
Active Comparator
Arm Description
CAT with FG and Tranilast and MMC 0.02%
Arm Title
Control
Arm Type
Placebo Comparator
Arm Description
CAT with FG and MMC 0.02%
Intervention Type
Drug
Intervention Name(s)
Tranilast, and Tissucol
Other Intervention Name(s)
Rizaben, Tissucol
Intervention Description
1.0%, 0.1 ml, subconjunctival route, single dose
Intervention Type
Other
Intervention Name(s)
Beriplast P
Other Intervention Name(s)
Tissucol
Intervention Description
0.1 ml to attach graft
Primary Outcome Measure Information:
Title
Recurrence rate at months six and twelve months Immunohistochemical and cell morphology analysis at the end of study, 12 months
Time Frame
6 and 12 months
Secondary Outcome Measure Information:
Title
Patient discomfort at day one, six and twelve months Safety of Tranilast
Time Frame
one day, 6 and 12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Primary pterygium Exclusion Criteria: Keratoconjunctivitis sicca Sjögren disease Vernal keratoconjunctivitis Acne rosacea Neurotrophic keratopathy Severe dysfunction of the meibomius glands Use of any immunosuppressive drug, through systemic and topical route Aged under 18 years of age and vulnerable groups Glaucoma and use of ocular hipotensor
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Gildasio C Almeida Jr, Prof Dr
Organizational Affiliation
Sao Jose do Rio Preto Medical School
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Sidney JF Sousa, Prof Dr
Organizational Affiliation
USP - Ribeirão Preto
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Reinaldo Azoubel, Prof Dr
Organizational Affiliation
Prof Dr
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Vinicius Tadeu NS Nascimento, Student
Organizational Affiliation
Sao Jose do Rio Preto Medical School
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Acacio AS Lima Filho, MD
Organizational Affiliation
Federal University of São Paulo
Official's Role
Study Chair
Facility Information:
Facility Name
Hospital de Base/FAMERP
City
Sao Jose do Rio Preto
State/Province
Sao Paulo
ZIP/Postal Code
15090-000
Country
Brazil

12. IPD Sharing Statement

Citations:
PubMed Identifier
18053915
Citation
Wang M, Zhang JJ, Jackson TL, Sun X, Wu W, Marshall J. Safety and efficacy of intracapsular tranilast microspheres in experimental posterior capsule opacification. J Cataract Refract Surg. 2007 Dec;33(12):2122-8. doi: 10.1016/j.jcrs.2007.07.041.
Results Reference
result
PubMed Identifier
15307986
Citation
Ji CN, Hu YZ, Ding ZP, Li GG. [The investigation of tranilast on the proliferation and migration of human Tenon's capsule fibroblasts]. Zhonghua Yan Ke Za Zhi. 2004 Mar;40(3):165-9. Chinese.
Results Reference
result
PubMed Identifier
12297693
Citation
Yasukawa T, Kimura H, Dong J, Tabata Y, Miyamoto H, Honda Y, Ogura Y. Effect of tranilast on proliferation, collagen gel contraction, and transforming growth factor beta secretion of retinal pigment epithelial cells and fibroblasts. Ophthalmic Res. 2002 Jul-Aug;34(4):206-12. doi: 10.1159/000063884.
Results Reference
result
PubMed Identifier
25714528
Citation
Almeida Junior GC, Arakawa L, Santi Neto Dd, Cury PM, Lima Filho AA, Sousa SJ, Alves MR, Azoubel R. Preoperative tranilast as adjunctive therapy to primary pterygium surgery with a 1-year follow-up. Arq Bras Oftalmol. 2015 Jan-Feb;78(1):1-5. doi: 10.5935/0004-2749.20150002.
Results Reference
derived

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Evaluation of Tranilast to Treat Pterygium Before Excision

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