CClinicalTrials.gg
Status unknownNCT02015000Updated Dec 19, 2013

Surgical Result of Pterygium Extended Removal Followed by Fibrin Glue Assisted Amniotic Membrane Transplantation

An interventional study of P.E.R.F.A.M.T in Pterygium and Recurrence, sponsored by National Taiwan University Hospital. Status unknown at 1 site in Taiwan. Open to participants aged 18 Years to 90 Years. Per ClinicalTrials.gov, last updated 2013-12-19.

Sponsored by National Taiwan University Hospital · Not applicable, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Dec 2013), so the status shown — last known as Recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
60
Allocation
Not applicable
Ages
18 Years to 90 Years
Sex
All
01

Study summary

The treatment of pterygium is still quite controversial. Previous studies using a large incision for pterygium excision and a large graft and has reported a very low recurrence rate with the P.E.R.F.E.C.T. technique. However, the P.E.R.F.E.C.T. technique is a relatively lengthy procedure and may not be suitable for patient with limited conjunctival reserve. Thus, we try to evaluate the final outcome of a sutureless amniotic membrane transplant technique combining the extended pterygium excision in hope to avoid the complication of the P.E.R.F.E.C.T. for PTERYGIUM technique.

Read the detailed description

The treatment of pterygium is still quite controversial. There is a lack of consensus in the ophthalmological community about the optimal surgical management of pterygia. The main challenge to successful surgical treatment of pterygium is recurrence, evidenced by fibrovascular growth across the limbus onto the cornea.

Previous studies using a large incision for pterygium excision and a large graft and has reported a very low recurrence rate with the P.E.R.F.E.C.T. technique. However, the P.E.R.F.E.C.T. for PTERYGIUM technique is not that perfect since it is a lengthy procedure, requires meticulous handling of tissue, and is associated with significant postoperative pain and, frequently, transient diplopia. Therefore, we try to evaluate the final outcome of a sutureless amniotic membrane transplant technique combining the extended pterygium excision in hope to avoid the complication of the P.E.R.F.E.C.T. for PTERYGIUM technique. This sutureless technique with the tissue glue may promote increased clinical use of amniotic membrane patch by alleviating patients' pain and shortening surgical time.

02

Conditions studied

  • Pterygium
  • Recurrence

Keywords

  • Pterygium
  • Recurrence
03

In context

Pterygium

111 studies on the registry are indexed under Pterygium; 10 are open to participants now.

This study's planned enrollment of 60 is close to the median of 60 across 92 interventional studies indexed under Pterygium.

Browse Pterygium studies →

Lead sponsor

National Taiwan University Hospital is the lead sponsor of 2,563 studies on the registry; 569 are open to participants now.

Of its 11 completed or terminated interventional studies of FDA-regulated products, 2 (18%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 90 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Patient with pterygium
  • Operated by single surgeon (Chen, Wei-Li)

Exclusion criteria

Exclusion Criteria:

  • Follow-up time less than 12 months
  • Age less then 18 year-old
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
60 participants (estimated)

Study arms

  • Experimental
    pterygium recurrence

    Surgical Result of Primary and Recurrent Pterygium by Using Pterygium Extended Removal followed by Fibrin Glue Assisted Amniotic Membrane Transplantation (P.E.R.F.A.M.T)

    Procedure: P.E.R.F.A.M.T

Interventions

  • ProcedureP.E.R.F.A.M.T

    Surgical Result of Primary and Recurrent Pterygium by Using Pterygium Extended Removal followed by Fibrin Glue Assisted Amniotic Membrane Transplantation (P.E.R.F.A.M.T)

06

What researchers measure

Primary outcomes

  1. Recurrence of pterygium

    defined as proliferating conjunctival tissue was found extending the limbus more than 1 mm onto the cornea within the surgical field )

    Time frame: 1 year

Secondary outcomes

  1. caruncular morphology

    A grading scale of 1 to 4 for the caruncle morphological characteristics was designed. Grade 1 with a normal appearance of the operated site; Grade 2 with the presence of fine episcleral vessels in the excised area, extending to the limbus, but without any fibrous tissue; Grade 3 with fibrovascular tissue in the excised area, reaching to the limbus but not invading the cornea; Grade 4 with aA true corneal recurrence, with fibrovascular tissue invading the cornea and across the limbus.

    Time frame: 1 year

07

Study locations

1 of 1 sites recruiting
  • National Taiwan University Hospital
    Taipei, Taipei City 100, Taiwan
    • Hsin-Yu Liu · Contact · singhuh@gmail.com · 886928779756
    • Hsin-Yu Liu · Sub investigator
    Recruiting
08

References and documents

Publications

  • Hirst LW. Prospective study of primary pterygium surgery using pterygium extended removal followed by extended conjunctival transplantation. Ophthalmology. 2008 Oct;115(10):1663-72. doi: 10.1016/j.ophtha.2008.03.012. Epub 2008 Jun 16. PubMed 18555531 ↗
  • Hirst LW. Recurrent pterygium surgery using pterygium extended removal followed by extended conjunctival transplant: recurrence rate and cosmesis. Ophthalmology. 2009 Jul;116(7):1278-86. doi: 10.1016/j.ophtha.2009.01.044. PubMed 19576496 ↗
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 19, 2013, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT02015000
Lead sponsor
National Taiwan University Hospital
Responsible party
Sponsor
First posted
Dec 19, 2013
Start date
Nov 2013
Primary completion
Dec 2013 (estimated)
Completion
Nov 2014 (estimated)
Last update
Dec 19, 2013

Study contacts

Hsin-Yu y Liu
Contact
singhuh@gmail.com
886829779756
Wei-Li Chen
study director · National Taiwan University Hospital

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

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This study is status unknown, as verified in Dec 2013. You cannot join it, but the record below documents what was studied.

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