To Compare Fibrin Glue and Suture in Primary Pterygium Excision With Amniotic Membrane Transplantation
This study has been completed.
Sponsor:
Chulalongkorn University
Information provided by:
Chulalongkorn University
ClinicalTrials.gov Identifier:
NCT00457223
First received: April 4, 2007
Last updated: February 12, 2008
Last verified: February 2008
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Purpose
The purpose of this study is to compared between conventional pterygium excision and AMT transplantation with suture and with fibrin glue.
| Condition | Intervention | Phase |
|---|---|---|
|
Pterygium |
Procedure: Amniotic membrane transplantation using fibrin glue |
Phase 2 Phase 3 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | Randomized Controlled Trial to Compare Fibrin Glue and Suture in Primary Pterygium Excision With Amniotic Membrane Transplantation |
Further study details as provided by Chulalongkorn University:
Primary Outcome Measures:
- Pain and discomfort during and after surgery using visual analog scale [ Time Frame: during surgery and after surgery up to 30 days ] [ Designated as safety issue: No ]
Secondary Outcome Measures:
- Surgical time [ Time Frame: start and to the end of surgery ] [ Designated as safety issue: No ]
- Healing of epithelial defect on cornea and AMT [ Time Frame: until 30 days ] [ Designated as safety issue: No ]
- Postoperative inflammation [ Time Frame: up to 30 days ] [ Designated as safety issue: Yes ]
- Complications e.g. Recurrent, graft loss/dehiscent, re-operation [ Time Frame: until last follow up ] [ Designated as safety issue: Yes ]
| Enrollment: | 32 |
| Study Start Date: | April 2007 |
| Study Completion Date: | August 2007 |
| Primary Completion Date: | August 2007 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: 1Fibrin glue
After pterygium excision, amniotic membrane was shaped and attached to bare scleral area using fibrin glue (Quixil®)
|
Procedure: Amniotic membrane transplantation using fibrin glue
After pterygium excision, amniotic membrane was shaped and attached to bare scleral area using fibrin glue (Quixil®) in 16 eyes of 16 patients of FG group and continuous suture with nylon 10-0 in 16 eyes of 16 patients of SU group.
Other Names:
|
|
Active Comparator: 2 Suture
After pterygium excision, amniotic membrane was shaped and attached to bare scleral area using continuous suture with nylon 10-0
|
Procedure: Amniotic membrane transplantation using fibrin glue
After pterygium excision, amniotic membrane was shaped and attached to bare scleral area using fibrin glue (Quixil®) in 16 eyes of 16 patients of FG group and continuous suture with nylon 10-0 in 16 eyes of 16 patients of SU group.
Other Names:
|
Detailed Description:
There are few studies about use of fibrin glue in pterygium surgery with conjunctival auto-graft with promising outcome. Less recurrent rate, less discomfort and halve surgical time were reported.
Up to our knowledge,there is no report of fibrin glue in pterygium excision with amniotic membrane transplantation(AMT). There is conventional technique to use AMT in King Chulalongkorn Memorial Hospital because some benefits over conjunctival auto-graft e.g.
- Preserve healthy superior conjunctiva for future glaucoma filtering surgery
- Can use in big or 2-headed pterygium
- Not contract as conjunctival graft esp. in case of fibrin glue
- Potential easier to use with fibrin glue
- Available from Thai Red Cross Eye Bank Comparison(s): amniotic membrane transplantation using fibrin glue compare to suture after pterygium excision.
Eligibility| Ages Eligible for Study: | 18 Years to 80 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- primary pterygium
Exclusion Criteria:
- Pregnant women
- Recurrent pterygium
- Pseudopterygium
- Uncontrolled systemic disease.
- Known allergy to any of the study agents or preservatives used in the formulations.
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00457223
Locations
| Thailand | |
| Department of Ophthalmology, King Chulalongkorn Memorial hospital | |
| Bangkok, Thailand, 10330 | |
Sponsors and Collaborators
Chulalongkorn University
Investigators
| Study Chair: | Ngamjit Kasetsuwan, MD | Ophthalmology Department, Faculty of Medicine, Chulalongkorn University |
More Information
No publications provided
| Responsible Party: | Ratchadapiseksompotch Fund, Chulalongkorn University, Faculty of Medicine |
| ClinicalTrials.gov Identifier: | NCT00457223 History of Changes |
| Other Study ID Numbers: | 401/49 |
| Study First Received: | April 4, 2007 |
| Last Updated: | February 12, 2008 |
| Health Authority: | Thailand: Ethical Committee |
Keywords provided by Chulalongkorn University:
|
pterygium pterygia excision |
amniotic membrane transplantation fibrin glue suture |
Additional relevant MeSH terms:
|
Pterygium Conjunctival Diseases Eye Diseases Fibrin Tissue Adhesive Hemostatics |
Coagulants Hematologic Agents Therapeutic Uses Pharmacologic Actions |
ClinicalTrials.gov processed this record on June 13, 2013