- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00704977
Alcohol 20% for Separation of Pterygium and Comparison of Different Wound Closure Methods
Evaluation of Alcohol 20% for Separation of Pterygium Tissue During Pterygium Surgery and Comparison of Three Different Methods of Wound Closure in Pterygium Surgery: Bare Sclera, Sliding Flap, Amniotic Membrane With Biological Glue
Study Overview
Status
Conditions
Detailed Description
Pterygium is a fibrovascular tissue growing on conjunctiva and cornea. The disturbance/morbidity caused by pterygium is diverse, ranging from mild esthetic disturbance and till recurrent inflammations and significant decrease of visual acuity. Rate of pterygium is between 20%-49% of general population, while increase in these numbers is observed in the population of equatorial regions. Pterygium usually appears at age of 22-49 years. While the rate of pterygium appearance increases with the age, the recurrence rate after surgical removal is higher in younger patients. Treatment of pterygium is surgical. The main challenges during surgery are peeling of pterygium and prevention of recurrence. During the last two decades several methods were developed and became widely accepted for pterygium surgery. The emphasis in modifying pterygium surgery is done on initial phase of surgery - techniques of pterygium separation and the final phase - the wound closure methods, additionally adjuncts (such as Mitomycine C) became widely used. These modifications are considered to improve the surgical outcomes and decrease the rate of complications and recurrence rate. Currently popular techniques of pterygium separation include Blunt dissection + keratectomy (blunt separation of the tissue + dissection of superficial layers of cornea); Avulsion technique (Avulsion of the pterygium head by creating tension on the cap edge+ further optional blunt dissection); Air assisted dissection (injection of air into the side of pterygium cap to create good separation plane).
Alcohol 20% is widely used in surface refractive surgery, where it helps to peel easily the epithelium of the cornea. Several reports show a positive role of alcohol in treatment of recurrent corneal erosions resistant to other treatments. At microscopic level - the ethanol splits basement membrane at the level between lamina lucida and lamina densa, additionally ethanol destroys the hemidesmosome junctions between epithelial cells. No consensus exists on ethanol influence on keratocyte viability and function: some studies show delayed wound healing and significant keratocyte damage, while other works show no significant alteration in keratocyte number while using alcohol.
At the phase of pterygium separation our purpose is to check the safety and efficiency of alcohol 20% for peeling of pterygium from ocular surface.
Various closure techniques exist, 3 of the widespread techniques are: Bare sclera (with adjunct such as mitomycine C) - the wound is left as it is, without closure. Sliding conjunctival flap- conjunctiva from adjacent region is dissected, moved to the wound area and sutured. Amniotic membrane transplantation, using biological glue to adhere the membrane. Amniotic membrane does not carry HLA antigens - so that no HLA compatibility tests are needed. Amniotic membrane underwent screening of infectious diseases and was cryopreserved. Amniotic membrane is applied with its mesenchimal part towards sclera and basement membrane side upwards. Adhesion of amniotic membrane is achieved by biological glue (containing thrombin and calcium as main ingredients)
We intend to compare each of these methods of wound closure in conjunction with using alcohol 20 % for pterygium separation.
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Tova Lifshitz, MD
- Phone Number: 972-8-6400288
- Email: toval@bgu.ac.il
Study Contact Backup
- Name: Anry Pitchkhadze, MD
- Phone Number: 972-8-6400556
- Email: anrypi@clalit.org.il
Study Locations
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-
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Beer Sheva, Israel
- Recruiting
- Soroka University Medical Center
-
Contact:
- Tova Lifshitz, MD
- Phone Number: 972-8-6400288
- Email: toval@bgu.ac.il
-
Contact:
- Anry Pitchkhadze, MD
- Phone Number: 972-8-6400556
- Email: anrypi@clalit.org.il
-
Principal Investigator:
- Tova Lifshitz, MD
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Sub-Investigator:
- Erez tsumi, MD
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Sub-Investigator:
- Anry Pitchkhadze, MD
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Sub-Investigator:
- Tova Monos, MD
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Sub-Investigator:
- Jaime Levy, MD
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Sub-Investigator:
- Avichai Segal, MD
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Sub-Investigator:
- Aliona Petrova, MD
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Sub-Investigator:
- Zach Ashkenazi, MD
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Sub-Investigator:
- Boris Knyazer, MD
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Sub-Investigator:
- Noam Yankulovich, MD
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Sub-Investigator:
- Ahed Amtirat, MD
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Beer Sheva, Israel
- Recruiting
- Soroka University Medical Center, Ophthalmology department and outpatient clinics
-
Contact:
- Tova Lifshitz, MD
- Phone Number: 972-8-6400288
- Email: toval@bgu.ac.il
-
Contact:
- Anry Pitchkhadze, MD
- Phone Number: 972-8-6400556
- Email: anrypi@clalit.org.il
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Age- above 18 years old.
- Primary pterygium.
- Eligibility to sign the informed consent.
Exclusion Criteria:
- Unwillingness to participate in study.
- Hypersensitivity to materials/ medications used during the surgery.
- Pregnancy.
- Cases when the eye which should be operated is the only fuctional eye.
- Age less than 18 years old.
- Recurrent pterygium.
- Chronic eye diseases, especially ocular surface disorders such as: OCP, severe blepharitis, severe keratoconjunctivitis,atopic eye disorders.
Patients which are not eligible to sign independently the informed consent.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: TREATMENT
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
ACTIVE_COMPARATOR: 1
Pterygium surgery using alcohol 20% + wound closure by bare sclera technique
|
The eye operated is disinfected and covered according routine protocol. Tightly applying well above the pterygium area. Instilling alcohol 20% into the well and holding for 40-60 seconds. Absorbing alcohol by applicator and abundant irrigation with BSS. Pterygium separation starting 2 mm centrally from the edges of the tissue. Excising the pterygium tissue at the base. Applying mytomycin C for 2.5 min+ abundant irrigation with BSS. Wound closure by by technique described in each arm. Bandage with chloramphenicol ointment or with Maxitrol ointment (Dexamethasone/Neomycin/Polymyxin B Eye Ointment. Postoperative treatment include :antibiotic and steroid eyedrop treatment at least 2 weeks. Follow up at 1 week, 1 month, 3 months, 6 months, 1 year. If additional follow upvisits are needed - they will be accomplished according the patients condition and needs. |
ACTIVE_COMPARATOR: 2
Alcohol 20% for pterygium separation + wound closure by sliding flap technique. The main steps of surgery are described below.Wound closure technique is as follows. Disection of conjunctiva adjascent to the wound, bringing the dissected conjunctiva to the wound area and suturing by vicril 6/0 sutures |
The eye operated is disinfected and covered according routine protocol. Tightly applying well above the pterygium area. Instilling alcohol 20% into the well and holding for 40-60 seconds. Absorbing alcohol by applicator and abundant irrigation with BSS. Pterygium separation starting 2 mm centrally from the edges of the tissue. Excising the pterygium tissue at the base. Applying mytomycin C for 2.5 min+ abundant irrigation with BSS. Wound closure by by technique described in each arm. Bandage with chloramphenicol ointment or with Maxitrol ointment (Dexamethasone/Neomycin/Polymyxin B Eye Ointment. Postoperative treatment include :antibiotic and steroid eyedrop treatment at least 2 weeks. Follow up at 1 week, 1 month, 3 months, 6 months, 1 year. If additional follow upvisits are needed - they will be accomplished according the patients condition and needs. |
ACTIVE_COMPARATOR: 3
Alcohol 20 % for pterygium separation + using amniotic membrane and biological glue for wound closure. The steps of surgery are as described below, wound closure technique is as follows. Amniotic membrane is applied with its mesenchimal side to conjunctiva and glued by biological glue (main ingradients: calcium and thrombin) |
The eye operated is disinfected and covered according routine protocol. Tightly applying well above the pterygium area. Instilling alcohol 20% into the well and holding for 40-60 seconds. Absorbing alcohol by applicator and abundant irrigation with BSS. Pterygium separation starting 2 mm centrally from the edges of the tissue. Excising the pterygium tissue at the base. Applying mytomycin C for 2.5 min+ abundant irrigation with BSS. Wound closure by by technique described in each arm. Bandage with chloramphenicol ointment or with Maxitrol ointment (Dexamethasone/Neomycin/Polymyxin B Eye Ointment. Postoperative treatment include :antibiotic and steroid eyedrop treatment at least 2 weeks. Follow up at 1 week, 1 month, 3 months, 6 months, 1 year. If additional follow upvisits are needed - they will be accomplished according the patients condition and needs. |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
postoperative complications
Time Frame: during first 3 months
|
during first 3 months
|
pterygium recurrence
Time Frame: at least 1 year
|
at least 1 year
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
patient satisfaction
Time Frame: during 1 year
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during 1 year
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corneal topography
Time Frame: during 1 year
|
during 1 year
|
endothelial cell density
Time Frame: during 1 year
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during 1 year
|
evaluation of risk factors for pterygium recurrence (ex. exposure to UV-light, family history ...)
Time Frame: during 1 year
|
during 1 year
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Tova Lifshitz, MD, Professor, Chief of ophthalmology department and clinics, SorokaUniversity Medical Center, Israel
Study record dates
Study Major Dates
Study Start
Primary Completion (ANTICIPATED)
Study Completion (ANTICIPATED)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ESTIMATE)
Study Record Updates
Last Update Posted (ESTIMATE)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- sor471508ctil
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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