Clinical Trial: The Application of Fibrin Glue in Ocular Surface Diseases
This study is currently recruiting patients.
Verified by National Taiwan University Hospital March 2005
| Sponsored by: | National Taiwan University Hospital | | Information provided by: | National Taiwan University Hospital | | ClinicalTrials.gov Identifier: | NCT00155402 | |
Purpose
This clinicl trials try to use
tissue fibrin glues (Tissell) to treat various ocular surface diseases or surgerys, which includes pterygium surgery, corneal melting/perforation, Gunderson''''s flap,conjuntical laceration,and muscle/cintical/flitering
surgery | Condition | Intervention | Phase |
Pterygium Corneal Perforation Corneal Ulcer
| Drug: tissue fibrin glue application (Tisseel)
| Phase I
|
MedlinePlus related topics: Eye Diseases; Eye Injuries; Vision Impairment and Blindness
Study Type: Interventional
Study Design: Treatment, Non-Randomized, Open Label, Placebo Control, Single Group Assignment, Safety/Efficacy Study
Further Study Details:
Primary Outcomes: cure of the diseases; visual acuity; side effects
Secondary Outcomes: integrity of the ocular surface
Expected Total Enrollment: 30
Study start: April 2005; Expected completion: March 2008
This clinicl trials try to use
tissue fibrin glues (Tissell) to treat various ocular surface diseases or surgerys. The inclusion criteria is (1) ocular surface disease which may need amniotic
membrane transplantation (corneal prro epithelization, pterygium surgery, etc)(2) infectious or noninfectious corneal ulcer with perfoation less than 3 mm (3) conjuntical transplantation/suture (4)corneal sugeries which can be treated by conventional suture technique or applcation with cyanoacrylic acid
tissue glues.Inform consents will be obtained from the patients before applcatinos. 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.
Eligibility
Ages Eligible for Study: 3 Years and above, Genders Eligible for Study: Both
Criteria
Inclusion Criteria:
- ocular surface diseases, which are expected to be treated by tissue fibrin glues
Exclusion Criteria:
- preganancy, children younger than 3 years old
Location and Contact Information
Please refer to this study by ClinicalTrials.gov identifier NCT00155402
Wei-Li Chen 011-886-2-23123456 Ext. 5206 cwlboston@yahoo.com.tw
Taiwan Wei-Li Chen, Taiwan, 100, Taiwan; Recruiting
Fung-Rong Hu, MD 886-2-23123456 ext 5189 fungrong@ha.mc.ntu.edu.tw
Fung-Rong Hu, MD, Principal Investigator
Study chairs or principal investigators
Fung-Rong Hu, MD, Principal Investigator, National Taiwan University Hospital
More Information
Study ID Numbers: 940208
Last Updated: September 9, 2005
Record first received: September 8, 2005
ClinicalTrials.gov Identifier: NCT00155402
Health Authority: Taiwan: Department of Health
ClinicalTrials.gov processed this record on 2005-09-13
Source: ClinicalTrials.gov
Cache Date: September 14, 2005