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Corneal Epithelial Autograft for Pterygium

Primary Purpose

Pterygium

Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Corneal epithelial autograft
Limbal conjunctival autograft
Simple removal
Diamond knife
Femtosecond laser
Sponsored by
Chunxiao Wang
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Pterygium

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Age between 18 to 80 years old;
  2. Primary pterygium, scheduled for elective surgical excision;
  3. Pterygium encroaching from the nasal side onto the cornea, with less than 180° limbal involvement and without approaching the central visual axis (pupil area);
  4. Morphologically intact palisades of Vogt in a given limbal region;
  5. Absence of any one of the following structures in the limbal region underneath the pterygium: (1) epithelial basal cells with dark cytoplasm and reflective cell borders; (2) at least two prominent palisade ridge structures; (3) at least one circular and/or oval-shaped focal stromal projection;
  6. Informed consent signed by patient or legal guardian; Having the ability to comply with study assessments for the full duration of the study.

Exclusion Criteria:

  1. Limbal stem cell deficiency by ocular surface disorders other than pterygium;
  2. Inability to determine whether the palisades of Vogt underneath the pterygium is absent or not using in vivo confocal microscopy;
  3. High myopia with a spherical equivalent of -15.0 D or less;
  4. Corneal or ocular surface infection within 30 days prior to study entry;
  5. Ocular surface malignancy;
  6. Uncontrolled diabetes with most recent Hemoglobin A1c greater than 8.5%;
  7. Renal failure with creatinine clearance< 25ml/min;
  8. Alanine aminotransferase > 40IU/L, or aspartate aminotransferase > 40IU/L;
  9. Platelet levels < 150,000 or > 450,000 per microliter;
  10. Hemoglobin < 12.0 g/dL (male) or < 11.0 g/dL (female);
  11. Prothrombin time > 16s and activated partial thrombin time > 35s in patients not accepting anticoagulant therapy; An international normalized ratio greater than 3 in patients accepting anticoagulant therapy;
  12. Pregnancy (positive test) or lactation;
  13. Participation in another simultaneous medical investigation or clinical trial;
  14. Severe cicatricial eye disease;
  15. Ocular comorbidities that affect the prognosis of transplantation, such as advanced glaucoma or retinal diseases;
  16. Severe dry eye disease as determined by Schirmer's test < 2mm at least in one eye;
  17. Any medical or social condition that in the judgement of the investigator would interfere with or serve as a contraindication to adherence to the study protocol or ability to give informed consent;
  18. Signs of current infection, including fever and treatment with antibiotics;
  19. Active immunological diseases;
  20. History of allo-limbal transplantation, penetrating keratoplasty or anti-glaucoma filtering surgeries.

Sites / Locations

  • Zhongshan Ophthalmic Center, Sun Yat-sen UniverisityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Active Comparator

Active Comparator

Arm Label

Corneal epithelial autograft

Limbal conjunctival autograft

Simple removal

Arm Description

pterygium resection combined with femtosecond laser assisted corneal epithelial autograft

pterygium resection combined with diamond knife assisted limbal conjunctival autograft

Simple removal of pterygium

Outcomes

Primary Outcome Measures

Restoration of corneal surface
Restoration of a completely epithelized, stable, and avascular corneal surface

Secondary Outcome Measures

Recurrence of pterygium
To observe recurrence of pterygium using slit-lamp microscopy
Reconstruction of palisades of Vogt
To observe the reconstruction of palisades of Vogt using in vivo confocal microscopy.
Best corrected visual acuity
To assess changes of best corrected visual acuity using ETDRS chart
Corneal power and astigmatism
To assess changes of corneal power and astigmatism using autorefractor keratometer
Corneal haze measurement
To observe the scatter of corneal haze using in vivo confocal microscopy

Full Information

First Posted
July 12, 2017
Last Updated
February 21, 2018
Sponsor
Chunxiao Wang
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1. Study Identification

Unique Protocol Identification Number
NCT03217500
Brief Title
Corneal Epithelial Autograft for Pterygium
Official Title
A Randomized Controlled Clinical Trial of Corneal Epithelial Autograft for Pterygium
Study Type
Interventional

2. Study Status

Record Verification Date
February 2018
Overall Recruitment Status
Unknown status
Study Start Date
July 20, 2017 (Actual)
Primary Completion Date
December 30, 2018 (Anticipated)
Study Completion Date
December 30, 2019 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Chunxiao Wang

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
The purpose of the study is to explore whether femtosecond laser-assisted cornea epithelial autograft is more effective than limbal conjunctival autograft for ocular surface reconstruction after excision of pterygium.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pterygium

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
45 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Corneal epithelial autograft
Arm Type
Experimental
Arm Description
pterygium resection combined with femtosecond laser assisted corneal epithelial autograft
Arm Title
Limbal conjunctival autograft
Arm Type
Active Comparator
Arm Description
pterygium resection combined with diamond knife assisted limbal conjunctival autograft
Arm Title
Simple removal
Arm Type
Active Comparator
Arm Description
Simple removal of pterygium
Intervention Type
Procedure
Intervention Name(s)
Corneal epithelial autograft
Intervention Description
After removal of the recipient's pterygium tissue, a donor epithelial tissue equal in length to the bared limbus, will be obtained from the peripheral epithelial of the same eye (corneal epithelial autograft) using femtosecond laser technology. The epithelial graft will be sutured to the recipient limbal bed, with the goal of reconstruction of palisades of Vogt. The graft will act as a barrier to regrowth of pterygium. The area of the graft will be left with the Tenon capsule exposed.
Intervention Type
Procedure
Intervention Name(s)
Limbal conjunctival autograft
Intervention Description
After removal of the recipient's pterygium tissue, an adjustable diamond knife will be used to create a superficial circumferential incision at the corneal end of the limbal vascular arcade, equal in length to the bared limbus. This will be followed by harvesting the limbal-conjunctival flap. The limbal-conjunctival autograft will be sutured to the recipient bed, with the Tenon capsule exposed. The graft will serve as a barrier to regrowth of pterygium.
Intervention Type
Procedure
Intervention Name(s)
Simple removal
Intervention Description
Simple removal of the recipient's pterygium tissue, with the Tenon capsule exposed.
Intervention Type
Device
Intervention Name(s)
Diamond knife
Intervention Description
A diamond knife to create a particular shaped limbal graft for transplantation
Intervention Type
Device
Intervention Name(s)
Femtosecond laser
Intervention Description
A commercial femtosecond laser to create a particular shaped graft for transplantation
Primary Outcome Measure Information:
Title
Restoration of corneal surface
Description
Restoration of a completely epithelized, stable, and avascular corneal surface
Time Frame
1 year
Secondary Outcome Measure Information:
Title
Recurrence of pterygium
Description
To observe recurrence of pterygium using slit-lamp microscopy
Time Frame
1 year
Title
Reconstruction of palisades of Vogt
Description
To observe the reconstruction of palisades of Vogt using in vivo confocal microscopy.
Time Frame
1 year
Title
Best corrected visual acuity
Description
To assess changes of best corrected visual acuity using ETDRS chart
Time Frame
1 year
Title
Corneal power and astigmatism
Description
To assess changes of corneal power and astigmatism using autorefractor keratometer
Time Frame
1 year
Title
Corneal haze measurement
Description
To observe the scatter of corneal haze using in vivo confocal microscopy
Time Frame
1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age between 18 to 80 years old; Primary pterygium, scheduled for elective surgical excision; Pterygium encroaching from the nasal side onto the cornea, with less than 180° limbal involvement and without approaching the central visual axis (pupil area); Morphologically intact palisades of Vogt in a given limbal region; Absence of any one of the following structures in the limbal region underneath the pterygium: (1) epithelial basal cells with dark cytoplasm and reflective cell borders; (2) at least two prominent palisade ridge structures; (3) at least one circular and/or oval-shaped focal stromal projection; Informed consent signed by patient or legal guardian; Having the ability to comply with study assessments for the full duration of the study. Exclusion Criteria: Limbal stem cell deficiency by ocular surface disorders other than pterygium; Inability to determine whether the palisades of Vogt underneath the pterygium is absent or not using in vivo confocal microscopy; High myopia with a spherical equivalent of -15.0 D or less; Corneal or ocular surface infection within 30 days prior to study entry; Ocular surface malignancy; Uncontrolled diabetes with most recent Hemoglobin A1c greater than 8.5%; Renal failure with creatinine clearance< 25ml/min; Alanine aminotransferase > 40IU/L, or aspartate aminotransferase > 40IU/L; Platelet levels < 150,000 or > 450,000 per microliter; Hemoglobin < 12.0 g/dL (male) or < 11.0 g/dL (female); Prothrombin time > 16s and activated partial thrombin time > 35s in patients not accepting anticoagulant therapy; An international normalized ratio greater than 3 in patients accepting anticoagulant therapy; Pregnancy (positive test) or lactation; Participation in another simultaneous medical investigation or clinical trial; Severe cicatricial eye disease; Ocular comorbidities that affect the prognosis of transplantation, such as advanced glaucoma or retinal diseases; Severe dry eye disease as determined by Schirmer's test < 2mm at least in one eye; Any medical or social condition that in the judgement of the investigator would interfere with or serve as a contraindication to adherence to the study protocol or ability to give informed consent; Signs of current infection, including fever and treatment with antibiotics; Active immunological diseases; History of allo-limbal transplantation, penetrating keratoplasty or anti-glaucoma filtering surgeries.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Yingfeng Zheng, M.D.Ph.D.
Phone
+8613922286455
Email
yingfeng.zheng@qq.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Yizhi Liu, M.D.Ph.D.
Organizational Affiliation
Zhongshan Ophthalmic Center, Sun Yat-sen University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Ting Huang, M.D.Ph.D.
Organizational Affiliation
Zhongshan Ophthalmic Center, Sun Yat-sen University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Zhongshan Ophthalmic Center, Sun Yat-sen Univerisity
City
Guangzhou
State/Province
Guangdong
ZIP/Postal Code
510000
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Yingfeng Zheng, M.D. Ph.D.

12. IPD Sharing Statement

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Corneal Epithelial Autograft for Pterygium

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