Corneal Ulcer
Conditions
Keywords
CACICOL20
Brief summary
CACICOL20 is a biodegradable nanopolymer engineered to mimic glycosaminoglycans such as heparan sulfates. Applied to the corneal lesion, it replaces damaged heparan sulfates in the matrix scaffold. CACICOL20 binds to matrix proteins such as collagen and cytokines or endogenous growth factors of the cellular microenvironment. CACICOL20 provides a protective function and restores the matrix architecture. This produces a suitable spatial environment for cells to respond properly to the cascade of signals needed for tissue regeneration to resume. The ophthalmic solution, CACICOL20, used for corneal ulcers is very well tolerated both locally and generally, as proved by a pilot study which as been conducted at the Hôpital des XV-XX in Paris (France). It reduces the pain significantly and increases corneal ulcer healing (all ulcers treated were resistant to all other usual therapies). Therefore, the accuracy of a Randomized multicentric double blinded study to evaluate the efficacy of CACICOL20 versus placebo for chronic corneal ulcer healing has been shown and will begin mid-may 2010. In this study, CACICOL20 will be applied every 2 or 4 days for 3 months. The aim of the study is a double blinded comparison of complete chronic corneal ulcers healing rate within 3 months in 3 groups of patient double blinded randomized between CACICOL20 instillations distribution and physiological salt solution instillations distribution. The main judgment criteria is healing rate within 3 months defined as corneal ulcer complete closure.
Interventions
DEVICECACICOL20
CACICOL20 is a solution of dextran & poly(carboxymethylglucose sulphate)in physiological salt serum. CACICOL20 is presented in 0.33 mL strip. One drop is instilled at each application to impregnate cornea.
DEVICEPlacebo
It is the placebo of CACICOL20, containing dextran in physiological serum salt. It is presented, like CACICOL20, in a 0.33 mL strip. One drop is delivered at each application.
Sponsors
Assistance Publique - Hôpitaux de Paris
Organ, Tissue, Regeneration, Repair and Replacement
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No
Inclusion criteria
* Patients with non-infectious, corneal chronic ulcer, painful or not ,whose depth does not exceed the superficial stroma. * Resistance of corneal pathology to standard treatment: eye drops to promote healing, tear substitutes, anti-inflammatory drugs, cyclosporin. * Patients previously treated for the corneal pathology, assessed ineffective or Insufficiently effective by the investigator * Patients using wetting gel or eye drops without conservator during the inclusion * Anti-inflammatory local treatments must be stopped for at least 8 days. * No contact lenses or lenses must be removed for at least 8 days. * Age of inclusion ≥ 18 years. * Written and signed informed consent from patient. * Realization of a preliminary medical examination. * Covers by social insurance
Exclusion criteria
* Ulcers deeper than the superficial stroma, perforated ulcers or pre-perforated * Corneal abscess * Infectious and progressive ulcerative keratitis * Patients receiving anti-inflammatory eye drops or steroid with cyclosporine treatment (in this case, possibility of inclusion in the clinical protocol after a Case wash-out of 8 days) * Patients on long-term eye drops containing preservatives and can not be stopped or replaced by an equivalent without preservatives * Patients on systemic anti-inflammatory, anti-allergic, psychotropic or antibiotics therapies, modified since less than 10 days or likely to be on short-term * Wearing contact lenses if patient has not been stopped at least eight days before the start of the protocol * ocular surgery within the last 3 months * patient already included in another clinical trial with an investigational product * Pregnant patients or breastfeeding * Person under a legal protection measure, under guardianship * Unable to follow up medical examinations for geographical, social or psychological reasons * Not cover by social insurance.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Healing rate | Within 1 months | The main judgment criteria is healing rate within 3 months defined as corneal ulcer complete closure. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Healing rate | 2 and 3 months | Complete Healing rate of the ulcer at 1 and 2 months defined as corneal ulcer complete closure, the evaluation of the pain with visual pain scale and evaluation of the quotation of analgesic treatments used by the patient. |
| Visual pain scale | 1, 2 and 3 months | Complete Healing rate of the ulcer at 1 and 2 months defined as corneal ulcer complete closure, the evaluation of the pain with visual pain scale and evaluation of the quotation of analgesic treatments used by the patient. |
| Associated treatments quotation | 1, 2 and 3 months | Quotation of analgesic treatments used and assessment of the effects of lubricant eye drops on the patient. |
Countries
France
Outcome results
None listed