Comparison of Glue With Sutures for Pterygium Surgery

Sponsor
Wellington Hospital (Other)
Overall Status
Unknown status
CT.gov ID
NCT00326560
Collaborator
Baxter Healthcare Corporation (Industry)
40
1
16
2.5

Study Details

Study Description

Brief Summary

Pterygium excision surgery involves excising the abnormal growth from the cornea and filling the defect with a conjunctival (white of the eye) graft from the superior part of the eye. This is the best method of pterygium excision but it is recognised that in 10-15% of cases it will grow back (recurrence). Currently the investigators use small sutures to sew the graft in place. Recently it has been described that glue can be used instead of the sutures. It has been shown in one study that the patient discomfort is less and so is the surgical time. The investigators want to confirm these findings and also compare the recurrence rate between the two types of surgery. They plan to complete a prospective, randomised, control trial of 40 participants. Twenty will have traditional pterygium surgery with the conjunctival autograft sutured. Twenty will have cut and paste surgery with Tisseel glue. The two groups of participants will be compared for pain and discomfort, surgery time, and recurrence rate of the pterygia.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Pterygium excision and conjunctival autograft
Phase 3

Detailed Description

This is a prospective, randomised, control trial of 40 participants. Twenty patients in each arm. Twenty patients undergo standard pterygium excision with the conjunctival autograft sutured. Twenty patients undergo pterygium surgery with Tisseel glue replacing sutures as a method of attaching the conjunctival autograft. Participants will be reviewed, selected, and consented on a pre-assessment day. Surgery will be performed 10 at a time on an all day surgery operating list. Randomisation of the surgery type will be done at the time of surgery after the pterygium has been excised and the autograft taken. One surgeon (R. Hall) will perform all of the procedures. Follow-up will occur at week 1, 2, 4, 26, 52. A questionnaire answered by participants will indicate their pain, foreign body sensation, tearing, and discomfort. There will be observation of any complications such as graft failure and recurrence rate. Photographs will be taken pre-op and post-op.

Study Design

Study Type:
Interventional
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single
Primary Purpose:
Treatment
Official Title:
Comparison of Cut and Paste With Sutured Autograft Pterygium Excision
Study Start Date :
May 1, 2006
Study Completion Date :
Sep 1, 2007

Outcome Measures

Primary Outcome Measures

  1. Surgery time []

  2. Patient discomfort at day one, week one, two, four []

  3. Recurrence rate at months three, six, twelve []

Eligibility Criteria

Criteria

Ages Eligible for Study:
20 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Primary pterygium
Exclusion Criteria:
  • Ocular surface disease

  • Previous pterygium surgery

Contacts and Locations

Locations

Site City State Country Postal Code
1 Wellington Ophthalmology Department, Capital Coast District Health Board Wellington New Zealand 6001

Sponsors and Collaborators

  • Wellington Hospital
  • Baxter Healthcare Corporation

Investigators

  • Principal Investigator: Reece C Hall, MBChB, Capital Coast District Health Board

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
, ,
ClinicalTrials.gov Identifier:
NCT00326560
Other Study ID Numbers:
  • CEN/06/03/021
First Posted:
May 17, 2006
Last Update Posted:
Jun 16, 2006
Last Verified:
May 1, 2006
Keywords provided by , ,
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 16, 2006