Title

Effects of Topical Low Dose Preservative-free Hydrocortisone on Intraocular Pressure
Effects of Topical Low Dose Preservative-free Hydrocortisone on Intraocular Pressure in Patients With and Without Glaucoma
  • Phase

    N/A
  • Study Type

    Interventional
  • Status

    Completed No Results Posted
  • Study Participants

    90
Evaluation of the safety and efficacy of hydrocortisone eye drops in the treatment of OSD (ocular surface disease) patients with and without glaucoma.
The ocular surface comprises the cornea, conjunctiva, eyelids and lacrimal glands and any disorder in these structures can be classified as an ocular surface disorder (OSD). OSD includes Dry Eye Disease (DED), blepharitis and meibomian gland dysfunction (MDG), allergic eye diseases (AED), chemical and thermal burns; all these conditions can severely affect eyesight and quality of life, and sometime even blindness. Patients with OSD can develop photophobia, corneal scarring, intermittent blurred vision, pain, limited ability to perform daily activities, reduced vitality, poor general health and, in many cases, depression.

Glaucoma, one of the leading causes of irreversible blindness, is an optic neuropathy characterized by thinning of retinal nerve fiber layer and increase of optic disc cupping , whose main risk factor is closely related to the intraocular pressure (IOP) levels. Thus, the management of the disease consists in the lowering IOP through medical, laser or surgical therapy . However, IOP reduction is most commonly achieved using topical ocular medications, which often contain preservatives employed to maintain stability and sterility of the product. Preservatives can be associated with undesirable adverse effects such as allergy, local irritation and inflammation . The long-term use of anti-glaucoma medications produces several alterations of ocular surface components, especially at the conjunctival level where epithelial modifications, dendritic cell activation, conjunctiva-associated lymphoid tissue activation, and goblet cell (GCs) loss easily occur GCs play crucial tasks in the homeostasis of the ocular surface being the main source of mucoproteins, essential to maintain tear film stability. Thus, the loss of GCs progressively leads to the happening of an iatrogenic OSD . Moreover, advancing age is a significant risk factor for both OSD and glaucoma, further complicated by treatments for each condition, which can interact among them and yield counterproductive effects . For these reason glaucoma is often associated with OSD .Ocular surface inflammation is crucial in the pathophysiology of OSD, therefore anti-inflammatory therapy, including corticosteroids, may be of benefit to OSD patients . However, in susceptible individuals steroid-induced glaucoma or ocular hypertension can occur after steroid use. Individuals who develop an increase in IOP following steroid use are referred to as "steroid responders" . In a recent study Kallab et al. have found that dry eye treatment with low hydrocortisone dose reduced ocular inflammation without inducing increases in IOP ; glaucomatous patients were excluded from this study. Herein we evaluate the safety and efficacy of hydrocortisone eye drops in the treatment of OSD patients with and without glaucoma.
Study Started
Nov 04
2019
Primary Completion
Mar 04
2020
Study Completion
Mar 04
2020
Last Update
Oct 01
2021

Drug Hydrocortisone (CORTIVIS ®)

Once enrolled all the patients had to instill topical low dose (1,005 mg) preservative-free hydrocortisone (CORTIVIS ®- Medivis, Catania, Italy) 2 times daily in each eye for two weeks.

Group A: glaucoma Experimental

OSD patients with glaucoma

Group B: no glaucoma Active Comparator

OSD patients without glaucoma

Criteria

Inclusion Criteria:

age of at least 18 years
diagnosis of OSD (Ocular Surface Disease)
normal ophthalmic findings except history of OSD for at least 3 months, and current therapy with topical lubricants for at least 3 months
POAG (primary open-angle glaucoma ) patients on medical therapy

Exclusion Criteria:

clinically significant slit lamp findings at screening visit except OSD
participation in a clinical trial in the 4 weeks preceding the screening visit
symptoms of a clinically relevant illness in the 3 weeks before the screening visit
presence/ history of a severe medical or surgical condition
intake of parasympathomimetic or antipsychotic drugs
wearing of contact lenses
previous refractive laser surgery (e.g photorefractive keratectomy-PRK, laser assisted in situ keratomileusis-LASIK, etc.)
history of IOP increase caused by systemic or topical treatment with corticosteroids
IOP greater than 22 mmHg
treatment with corticosteroids in the 4 weeks preceding the study
types of glaucoma other than POAG
ocular infection or clinically significant inflammation
ocular surgery in the 3 months preceding the study
Sjögren's syndrome, Stevens-Johnson syndrome
history of allergic conjunctivitis
pregnancy, planned pregnancy or lactating
known hypersensitivity to any component of study medication
No Results Posted