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Femtosecond Laser-assisted Corneal Debridement for Herpes Simplex Keratitis

Primary Purpose

Herpes Simplex Keratitis

Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
FLDEB
Ganciclovir (GCV)
Femtosecond laser
Sponsored by
Chunxiao Wang
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Herpes Simplex Keratitis

Eligibility Criteria

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

Inclusion Criteria:

  1. Aged between 18 and 80 years old;
  2. Epithelial ulceration in a dendritic or geographic pattern, characteristic of infection with herpes simplex virus, and within 7 days of onset;
  3. Ulcer's stromal involvement < 120 micron, as indicated by anterior segment optical coherence tomography;
  4. 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. Clinical signs of a cause other than herpes simplex virus for the epithelial keratitis;
  2. Antivirus or corticosteroid treatment within 6 months;
  3. Active stromal keratitis or iritis;
  4. History of allergy or adverse reaction to ganciclovir;
  5. High myopia with a spherical equivalent of -15.0 D or less;
  6. Corneal or ocular surface infection within 30 days prior to study entry;
  7. Ocular surface malignancy;
  8. Uncontrolled diabetes with most recent Hemoglobin A1c greater than 8.5%;
  9. Renal failure with creatinine clearance< 25ml/min;
  10. Alanine aminotransferase > 40IU/L, or aspartate aminotransferase > 40IU/L;
  11. Platelet levels < 150,000 or > 450,000 per microliter;
  12. Hemoglobin < 12.0 g/dL (male) or < 11.0 g/dL (female);
  13. 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;
  14. Pregnancy (positive test) or lactation;
  15. Participation in another simultaneous medical investigation or clinical trial;
  16. Severe cicatricial eye disease; Conjunctival scarring with fornix shortening;
  17. Severe dry eye disease as determined by Schirmer's test < 2mm at least in one eye;
  18. 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;
  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 Type

Experimental

Active Comparator

Arm Label

FLDEB combined with GCV orally

GCV orally

Arm Description

Femtosecond laser-assisted cornea debridement (FLDEB) combined with ganciclovir (GCV) orally.

Ganciclovir (GCV) orally only

Outcomes

Primary Outcome Measures

Healing time
Time to complete corneal epithelial healing

Secondary Outcome Measures

Corneal re-epithelization
Assessing complete corneal re-epithelization at day 14±1 using slit-lamp microcopy
Corneal opacity and vascularization
Assessing corneal opacity and vascularization using slit-lamp microcopy
Best-corrected visual acuity
Assessing best-corrected visual acuity using ETDRS chart
Corneal power and astigmatism
Assessing changes of corneal power and astigmatism using autorefractor keratometer
Corneal sensation
Assessing corneal sensation using Cochet-Bonnet esthesiometer
Recurrence
Assessing recurrent HSK using slit-lamp microcopy

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
NCT03217474
Brief Title
Femtosecond Laser-assisted Corneal Debridement for Herpes Simplex Keratitis
Official Title
A Randomized Controlled Clinical Trial of Corneal Debridement for the Treatment of Herpes Simplex Epithelial Keratitis
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 learn if adding femtosecond laser-assisted corneal debridement to a standard therapy of oral ganciclovir can help shorten the healing time of herpes simplex epithelial keratitis (HSK).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Herpes Simplex Keratitis

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
FLDEB combined with GCV orally
Arm Type
Experimental
Arm Description
Femtosecond laser-assisted cornea debridement (FLDEB) combined with ganciclovir (GCV) orally.
Arm Title
GCV orally
Arm Type
Active Comparator
Arm Description
Ganciclovir (GCV) orally only
Intervention Type
Procedure
Intervention Name(s)
FLDEB
Other Intervention Name(s)
Femtosecond laser-assisted corneal debridement
Intervention Description
The eye will be anesthetized, and femtosecond laser technology will be used to remove epithelial tissue (diameter: 8mm; depth: 100micron) that includes the loosened diseased corneal epithelial cells. Antibiotic ointments and drops will be instilled postoperatively.
Intervention Type
Drug
Intervention Name(s)
Ganciclovir (GCV)
Intervention Description
Patient will be treated with GCV orally (200mg, 3 times a day, for 14 days).
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
Healing time
Description
Time to complete corneal epithelial healing
Time Frame
14 ± 1 days
Secondary Outcome Measure Information:
Title
Corneal re-epithelization
Description
Assessing complete corneal re-epithelization at day 14±1 using slit-lamp microcopy
Time Frame
14 ± 1 days
Title
Corneal opacity and vascularization
Description
Assessing corneal opacity and vascularization using slit-lamp microcopy
Time Frame
Baseline, 14 ± 1 days, 3 months
Title
Best-corrected visual acuity
Description
Assessing best-corrected visual acuity using ETDRS chart
Time Frame
Baseline, 14 ± 1 days, 3 months
Title
Corneal power and astigmatism
Description
Assessing changes of corneal power and astigmatism using autorefractor keratometer
Time Frame
Baseline, 14 ± 1 days, 3 months
Title
Corneal sensation
Description
Assessing corneal sensation using Cochet-Bonnet esthesiometer
Time Frame
Baseline, 14 ± 1 days, 3 months
Title
Recurrence
Description
Assessing recurrent HSK using slit-lamp microcopy
Time Frame
3 months

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: Aged between 18 and 80 years old; Epithelial ulceration in a dendritic or geographic pattern, characteristic of infection with herpes simplex virus, and within 7 days of onset; Ulcer's stromal involvement < 120 micron, as indicated by anterior segment optical coherence tomography; 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: Clinical signs of a cause other than herpes simplex virus for the epithelial keratitis; Antivirus or corticosteroid treatment within 6 months; Active stromal keratitis or iritis; History of allergy or adverse reaction to ganciclovir; 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; Conjunctival scarring with fornix shortening; 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; 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
5
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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Femtosecond Laser-assisted Corneal Debridement for Herpes Simplex Keratitis

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