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The Application of Fibrin Glue in Ocular Surface Diseases

Phase 1 Study of Applying Fibrin Glue in Patients With Corneal Ulcer or Patients Requiring Wound Closure by Suture

Status
Withdrawn
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00155402
Enrollment
30
Registered
2005-09-12
Start date
2005-04-30
Completion date
2008-03-31
Last updated
2008-05-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Corneal Ulcer, Pterygium

Keywords

fibrin glue, corneal perforation, pterygium, conjunctiva, corneal ulcer

Brief summary

This clinical trial tries to use tissue fibrin glues (Tisseel) to treat various ocular surface diseases or surgeries, which includes pterygium surgery, corneal melting/perforation, Gunderson's flap, conjunctival laceration, and muscle/clinical/filtering surgery.

Detailed description

This clinical trial tries to use tissue fibrin glues (Tisseel) to treat various ocular surface diseases or surgeries. The inclusion criteria are: 1. ocular surface disease which may need amniotic membrane transplantation (corneal pro epithelization, pterygium surgery, etc) 2. infectious or noninfectious corneal ulcer with perforation less than 3 mm 3. conjunctival transplantation/suture 4. corneal surgeries which can be treated by conventional suture technique or application with cyanoacrylic acid tissue glues. Informed consents will be obtained from the patients before applications. After surgeries, topical steroids and antibiotics will be used, and therapeutic contact lens will be used. The patients will be followed up for at least three months.

Interventions

DRUGtissue fibrin glue application (Tisseel)

Apply several droplets within several seconds to several minutes

Sponsors

National Taiwan University Hospital
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
3 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Ocular surface diseases, which are expected to be treated by tissue fibrin glues

Exclusion criteria

* Pregnancy * Children younger than 3 years old

Design outcomes

Primary

MeasureTime frame
cure of the diseases1week, 2 weeks, 3 weeks, 4 weeks

Secondary

MeasureTime frame
integrity of the ocular surface1week, 2 weeks, 3 weeks, 4 weeks
visual acuity1week, 2 weeks, 3 weeks, 4 weeks

Countries

Taiwan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026