The Application of Cultured Cornea Stem Cells in Patients Suffering From Corneal Stem Cell Insufficiency

Sponsor
National Taiwan University Hospital (Other)
Overall Status
Terminated
CT.gov ID
NCT01377311
Collaborator
(none)
0
1
1
21
0

Study Details

Study Description

Brief Summary

Name of the project:The application of cornea stem cells cultured on amniotic membrane in patients suffering from corneal stem cell insufficiency

Purpose: To develop the technique of using ex vivo expansion of autologous limbal stem cell cultured on amniotic membrane for treatment of patients suffering from limbal stem cell insufficiency

Condition or Disease Intervention/Treatment Phase
  • Procedure: Transplant of cultured limbal stem cells on cornea
Phase 1

Detailed Description

Materials and Methods:
  1. Patients suffering from unilateral limbal stem cell insufficiency will be chosen. Make sure those volunteers understand the benefits and risk factors of the operation.

  2. Prepare human amniotic membrane, and culture the membrane at37°C,5% CO2,95% room air.

  3. One month before transplantation, take 1-2mm2 of limbal tissues from the healthy eye, and culture the limbal tissue on amniotic membrane with 1.5 ml supplemental hormonal epithelial medium (in 5%的 fetal calf serum)

  4. Keep culturing the cells in Dulbecco's modified Eagle's medium/Ham's F12 (1:1 ratio), added with 5 % dimethyl sulfoxide, 2 mg/ml human epidermal growth factor ,5 ug/ml insulin, 0.5 ug/ml hydrocortisone, 50 ug/ml gentamicin, 1.25 ug/ml amphotericin B, 5% autoserum。Two to three weeks later, transplantation will be performed after the cells reaches 2-3 cm2

  5. Remove the abnormal surface tissue on the lesion cornea, transplant the amniotic membrane with cultured limbal stem cells on the denuded cornea. Cover with contact lens after operation, and apply topical antibiotics and steroids.

  6. Postoperatively, observe the patients for one week. After discharge, follow up the patients one week, two week, one month, two months, three months, six months and one year later.

  7. Pictures will be taken and the extent of corneal epithelium regeneration, visual acuity, and complications will be recorded during follow-up visits.

  8. The investigators plan to collect 20 patients from 1 July,2007 to 30, June, 2010

Study Design

Study Type:
Interventional
Actual Enrollment :
0 participants
Allocation:
Non-Randomized
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Phase 1 Study of Cornea Stem Cells Cultured on Amniotic Membrane Transplanted on Patients Suffering From Corneal Stem Cell Insufficiency
Study Start Date :
Jul 1, 2008
Actual Primary Completion Date :
Apr 1, 2010
Actual Study Completion Date :
Apr 1, 2010

Arms and Interventions

Arm Intervention/Treatment
Experimental: 1

Patients suffering from unilateral limbal stem cell insufficiency. Remove the abnormal surface tissue on the lesion cornea, transplant the amniotic membrane with cultured limbal stem cells on the denuded cornea. Cover with contact lens after operation, and apply topical antibiotics and steroids.

Procedure: Transplant of cultured limbal stem cells on cornea
Remove the abnormal surface tissue on the lesion cornea, transplant the amniotic membrane with cultured limbal stem cells on the denuded cornea. Cover with contact lens after operation, and apply topical antibiotics and steroids.

Outcome Measures

Primary Outcome Measures

  1. The extent of corneal epithelium regeneration [one week, two week, one month, two months, three months, six months and one year later]

Secondary Outcome Measures

  1. visual acuity [one week, two week, one month, two months, three months, six months and one year later]

  2. complications [one week, two week, one month, two months, three months, six months and one year later]

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • unilateral limbus defect larger than 180 degrees

  • repeated corneal epithelial ulcer, loss of visual acuity or neovascularization due to limbal stem cell insufficiency

  • no improvement after medical intervention for more than 6 months

  • the patient is willing to receive surgery and postoperative follow up

Exclusion Criteria:
  • bilateral limbus defect

  • limbal stem cell insufficiency does not induce repeated corneal epithelial ulcer, loss of visual acuity or neovascularization

  • corneal neovascularization deeper than 1/2 depth of surface matrix

  • peripheral surface matrix is less than 200um thick

  • no corneal reflex was induced by fiber less than 5mm length measured by Cocet-Bonnet esthesiometer

  • improvement under medication

  • perisurgical follow up less than 6 months

  • unable to be long term followed up postoperatively

  • glaucoma patients underwent glaucoma surgery, under medication, IOP > 21mmHg

  • glaucoma patients underwent glaucoma surgery, under medication, IOP < 21mmHg, optic disc depression > 90%

  • severe incomplete eyelid closure

  • severe dye eye syndrome, Schirmer test 5 min < 3 mm

  • contralateral eye limbus tissue cannot be obtained, or unable to be cultured

  • pregnant

Contacts and Locations

Locations

Site City State Country Postal Code
1 National Taiwan University Hospital, department of Ophthalmology Taipei Taiwan 10047

Sponsors and Collaborators

  • National Taiwan University Hospital

Investigators

  • Principal Investigator: Wei-Li Chen, MD, PhD, National Taiwan University Hospital, department of Ophthalmology

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
, ,
ClinicalTrials.gov Identifier:
NCT01377311
Other Study ID Numbers:
  • 32MD02
First Posted:
Jun 21, 2011
Last Update Posted:
Jun 21, 2011
Last Verified:
Jun 1, 2011

Study Results

No Results Posted as of Jun 21, 2011