Cauterization Versus fibrin Glue for Conjunctival Autografting in Primary Pterygium Surgery

Sponsor
University of Split, School of Medicine (Other)
Overall Status
Unknown status
CT.gov ID
NCT03321201
Collaborator
University Hospital of Split (Other)
164
1
2
43.8
3.7

Study Details

Study Description

Brief Summary

Pterygium is a noncancerous growth of the conjunctival tissue over the cornea. It is a progressive disease that may lead to visual impairment in advanced stages, as well as restriction of ocular motility, chronic inflammation and cosmetic concerns. Surgical removal is the treatment of choice, but recurrence of pterygium is a frequent problem. In this randomized controlled cauterization will be compared with fibrin glue for conjunctival autografting in primary pterygium surgery.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Cauterization
  • Procedure: Fibrin glue
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
164 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Triple (Participant, Investigator, Outcomes Assessor)
Masking Description:
Surgeons will not be blinded. All the other investigators, as well as study participants, outcome assessors and author that will analyze the data will be blinded.
Primary Purpose:
Treatment
Official Title:
Cauterization Versus fibrin Glue for Conjunctival Autografting in Primary Pterygium Surgery
Actual Study Start Date :
May 8, 2018
Anticipated Primary Completion Date :
May 1, 2020
Anticipated Study Completion Date :
Dec 31, 2021

Arms and Interventions

Arm Intervention/Treatment
Experimental: Cauterization

Procedure: Cauterization
To ensure the stability of the graft during cuttings, four sealing wraps will be installed, which will be removed after cauterisation is completed. Autograft and conjunctiva will be approximated by surgical forceps and will be cauterized using a bipolar cutter (Erbe ICC 50) with a force 1-3 / 20. Forceps will be released slowly to prevent elevation of the graft. The same procedure will be performed 10 times until graft is well firmed. Graft stability will be checked up with a sponge and additional cauterization will be preformed if needed.

Active Comparator: Fibrin glue

Procedure: Fibrin glue
Fiber adhesive (Tissel 1 mL kit4-iu) will be prepared according to manufacturer's instructions. Preparation time will be approximately 10-15 min per kit. Once mixed the fibrin glue is usable up to 4 h. For the purpose of the study preparation of the fibrin glue will be performed by a nurse.

Outcome Measures

Primary Outcome Measures

  1. Recurrence of pterygium [180 days]

    Any re-growth of tissue from the area of excision across the limbus onto the cornea.

Secondary Outcome Measures

  1. Surgical time [During the surgery]

    Surgical time: total operational time required for completion of the operation (measured in minutes)

  2. Complication rate [7, 30 and 180 days]

    Complication rate will be analyzed as the occurrence of at least one of the following major complications such as dehiscence, displacement or loss of the autograft, infection, haemorrhage, oedema, fibrosis, retraction and other indications that required special treatment

  3. Pterygium-induced astigmatism [7, 30 and 180 days]

    Measured as described by Hsu 2014

  4. Ocular surface condition [7, 30 and 180 days]

    The Ocular Surface Disease Index (OSDI) is a 12-question validated questionnaire used to measure ocular symptoms, visual function, and environmental factors that may affect a patient's vision. The OSDI scoring scale ranges from 0 to 100. The lower the score, the more symptomatic relief from dry eye symptoms a patient experiences. Baseline-adjusted scores were tabulated; a negative number change from baseline indicates a perceived improvement in ocular comfort.

  5. Postoperative discomfort, tearing, pain and foreign body sensation [7, 30 and 180 days]

    Using modified scale from Lim Bon Siong et al: (0) none, no pain, (1) very mild, (2) mild, pain causing some discomfort, (3) moderate, pain that partially interferes with usual activity or sleep, (4) sever, pain that completely interferes with usual activity or sleep.

  6. Pain [7, 30 and 180 days]

    Numerical rating scale (NRS) ranging from 0 to 10, where 0 = No pain and 10 = Pain as intense as you can imagine.

  7. Economic Analysis [180 days]

    Cost of each intervention

  8. Flap time [During the surgery]

    Time needed for preparing and repositioning of the conjunctival grafts (measured in minutes)

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion criteria:
  • adults (older than 18 years of age)

  • both sexes

  • primary nasal pterygia ˃4 mm, which tends to increase, including patients with reduced visual acuity, chronic inflammation, cosmetic reasons

  • if the patients had a bilateral pterygium, only one eye will be operated

Exclusion criteria:
  • connective tissue disease

  • prior eye surgery

  • chronic use of topical drugs (anti-glaucoma drugs)

Contacts and Locations

Locations

Site City State Country Postal Code
1 University Hospital Split Split Croatia 21000

Sponsors and Collaborators

  • University of Split, School of Medicine
  • University Hospital of Split

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Livia Puljak, Associate Professor, University of Split, School of Medicine
ClinicalTrials.gov Identifier:
NCT03321201
Other Study ID Numbers:
  • PTERYGIUM1
First Posted:
Oct 25, 2017
Last Update Posted:
Jun 5, 2019
Last Verified:
Jun 1, 2019
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 5, 2019