Recurrent Pterygium Clinical Trial
Official title:
Management of Recurrent Pterygium to Prevent Visual Impairment
Pterygium is a common eye disease. Its mechanism remains unknown but studies suggest that it
is related to exposure to ultraviolet rays and ocular dryness. Pterygium affects vision by
causing astigmatism and may encroach on cornea (transparent part of the eye) affecting
vision. It could cause ocular irritation and can be cosmetically unacceptable especially when
inflamed.
Recurrence is the most common outcome of pterygium excision. Recurrence rates of pterygium
vary from 10 to more than 80%. Recurrence can be detected first in the conjunctiva(skin of
your eye), before advancing on to the cornea. Treating the recurrent pterygium before the
cornea gets involved avoids repeat surgery, which is difficult and is associated with more
scarring. To avoid repeated surgeries, the activity of a recurrent pterygium should be
stopped before it progresses to true recurrence.
Several studies attributed the recurrence pf pterygium to the increase of substances as
vascular endothelial growth factor(VEGF) and fibroblast growth factor. Avastin (Anti-VEGF)
and 5 fluorouracil(5FU) (antimetabolite) are medications that suppress the formation of VEGF
and fibroblast growth factor.
Studies have shown that the subconjunctival injection of 5 F and Avastin into the recurring
pterygium has been both safe and effective in treatment of recurrent pterygium.
In many cases, vascularization and inflammation were controlled by subconjunctival Avastin,
providing evidence for a role of VEGF in pterygium formation. 5FU is widely used in
ophthalmology because of its anti-scarring properties.
The other option for treatment of recurrent pterygium is surgery. Recurrent pterygium is a
challenging condition that usually resists conventional surgery and its rate of recurrence
after surgery is high. Moreover, recurrent pterygium surgery is usually accompanied by
scarring, more risk of intra and post- complications This study aims to generate data to
inform further studies towards establishing Avastin and 5 fluouracil as treatment modality
for recurrent pterygium.
Purpose To assess the efficacy of combined 5FU and Avastin injections in the treatment of
recurrent pterygium.
Design Pilot study. The patients will receive combined 5FU and Avastin injection.
Methodology Patients for inclusion in the study will be identified in the specialist corneal
clinics at Queens Medical Centre.
5 FU injection
Dose: 0.15 ml of 5FU (3.75mg) will be administered into the body of the recurring pterygium
up to 5 injections as determined by response. The 5FU solution is prepared locally in the
pharmacy for ophthalmic use. It will be delivered preloaded in a 1ml syringe containing 0.3
ml of 2.5mg 5FU per 0.1ml. The injection will be given under topical anaesthesia. One to two
drops of 5% povidone iodine will be instilled in the conjunctival sac 5min before the
injection. All injections will be given in the outpatient clinic using a slit lamp. The
needle (27Gauge) will be advanced in a zigzag manner into the subconjunctival space, avoiding
any large blood vessels, until the middle of the lesion is reached. The solution will be then
injected and the needle withdrawn. After the injection, 1-2 drops of chloramphenicol 0.5%
preservative free minims will be instilled topically and continued four times a day for 3
days after each injection. Injections will be carried out every two weeks as described above.
Patients will have the ability to access the 24 hour on call emergency eye service, and at
the same time be provided with contact numbers for investigators for any queries during the
study period.
Avastin injection
Dose: 0.15 ml of Avastin (2.5 mg/0.1 ml) will be administered in the body of the recurrent
lesion. Up to 5 injections could be given.
The injection will be given under topical anaesthesia. One to two drops of 5% povidone iodine
will be instilled in the conjunctival sac 5min before the injection. All injections will be
given in the outpatient clinic using a slit lamp. The needle (27Gauge) will be advanced in a
zigzag manner into the subconjunctival space, avoiding any large blood vessels, until the
middle of the lesion is reached. The solution will be then injected and the needle withdrawn.
After the injection, 1-2 drops of chloramphenicol 0.5% preservativefree minims will be
instilled topically and continued four times a day for 3 days after each injection.
Injections will be carried out every two weeks as described above. Patients will have the
ability to access the 24 hour on call emergency eye service, and at the same time be provided
with contact numbers for investigators for any queries during the study period.
Fluorescein angiography (FFA) will be done to characterise the conjunctival vessels. It is a
safe routine investigation that is done on daily basis in eye clinics.
Patient Inclusion Criteria will be:
- Patients over the age of 18
- Able to give informed consent
- Patients with recurrent pterygium within 6 months of original excision[Recurrence is
defined in the protocol (page 22)]
- Use of effective contraception in females of childbearing age
Patient exclusion criteria will be:
- Patients under 18 years of age
- Patients unable or refusing to provide informed consent
- Patients who are needle phobic
- Pregnant women, women aiming for conception and breast feeding women.
- Patients with hypersensitivity to the active substance or to any of the excipients
- Patients with active or suspected ocular or periocular infections.
- Patients with active severe intraocular inflammation.
- Patients with raised intraocular pressure or on glaucoma medication
- Patients with advanced recurrent pterygium that extends between the pupil and limbus at
the time of presentation
In case of bilateral eye involvement, only one eye will be treated with the study drug. The
study participants will reserve the right to withdraw from the study at any stage, and will
be kept up to date with any new information available about the study medication.
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