Effects of Topical Low Dose Preservative-free Hydrocortisone on Intraocular Pressure
Primary Purpose
Ocular Surface Disease, Glaucoma
Status
Completed
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
Hydrocortisone (CORTIVIS ®)
Sponsored by

About this trial
This is an interventional treatment trial for Ocular Surface Disease
Eligibility 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
Sites / Locations
- University of Molise
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Group A: glaucoma
Group B: no glaucoma
Arm Description
OSD patients with glaucoma
OSD patients without glaucoma
Outcomes
Primary Outcome Measures
Intraocular pressure(IOP)
IOP evaluation at time zero (T0), after 1 (T1) and two weeks of therapy (T2).
OSDI (Ocular Surface Disease Index) questionnaire
OSDI record at time zero (T0), after 1 (T1) and two weeks of therapy (T2).
Secondary Outcome Measures
Full Information
NCT ID
NCT04536129
First Posted
August 27, 2020
Last Updated
September 30, 2021
Sponsor
University of Molise
Collaborators
Medivis
1. Study Identification
Unique Protocol Identification Number
NCT04536129
Brief Title
Effects of Topical Low Dose Preservative-free Hydrocortisone on Intraocular Pressure
Official Title
Effects of Topical Low Dose Preservative-free Hydrocortisone on Intraocular Pressure in Patients With and Without Glaucoma
Study Type
Interventional
2. Study Status
Record Verification Date
September 2021
Overall Recruitment Status
Completed
Study Start Date
November 4, 2019 (Actual)
Primary Completion Date
March 4, 2020 (Actual)
Study Completion Date
March 4, 2020 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Molise
Collaborators
Medivis
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Evaluation of the safety and efficacy of hydrocortisone eye drops in the treatment of OSD (ocular surface disease) patients with and without glaucoma.
Detailed Description
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ocular Surface Disease, Glaucoma
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
90 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Group A: glaucoma
Arm Type
Experimental
Arm Description
OSD patients with glaucoma
Arm Title
Group B: no glaucoma
Arm Type
Active Comparator
Arm Description
OSD patients without glaucoma
Intervention Type
Drug
Intervention Name(s)
Hydrocortisone (CORTIVIS ®)
Intervention Description
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.
Primary Outcome Measure Information:
Title
Intraocular pressure(IOP)
Description
IOP evaluation at time zero (T0), after 1 (T1) and two weeks of therapy (T2).
Time Frame
2 weeks
Title
OSDI (Ocular Surface Disease Index) questionnaire
Description
OSDI record at time zero (T0), after 1 (T1) and two weeks of therapy (T2).
Time Frame
2 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility 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
Facility Information:
Facility Name
University of Molise
City
Campobasso
Country
Italy
12. IPD Sharing Statement
Citations:
PubMed Identifier
29849435
Citation
Khanna RC. Ocular surface disorders. Community Eye Health. 2017;30(99):S1-S2. No abstract available.
Results Reference
result
PubMed Identifier
28797892
Citation
Craig JP, Nelson JD, Azar DT, Belmonte C, Bron AJ, Chauhan SK, de Paiva CS, Gomes JAP, Hammitt KM, Jones L, Nichols JJ, Nichols KK, Novack GD, Stapleton FJ, Willcox MDP, Wolffsohn JS, Sullivan DA. TFOS DEWS II Report Executive Summary. Ocul Surf. 2017 Oct;15(4):802-812. doi: 10.1016/j.jtos.2017.08.003. Epub 2017 Aug 8.
Results Reference
result
PubMed Identifier
31611797
Citation
Lanza M, Gironi Carnevale UA, Mele L, Bifani Sconocchia M, Bartollino S, Costagliola C. Morphological and Functional Evaluation of Oral Citicoline Therapy in Chronic Open-Angle Glaucoma Patients: A Pilot Study With a 2-Year Follow-Up. Front Pharmacol. 2019 Sep 26;10:1117. doi: 10.3389/fphar.2019.01117. eCollection 2019.
Results Reference
result
PubMed Identifier
32564453
Citation
Mohammed I, Kulkarni B, Faraj LA, Abbas A, Dua HS, King AJ. Profiling ocular surface responses to preserved and non-preserved topical glaucoma medications: A 2-year randomized evaluation study. Clin Exp Ophthalmol. 2020 Sep;48(7):973-982. doi: 10.1111/ceo.13814. Epub 2020 Jul 27.
Results Reference
result
PubMed Identifier
23215770
Citation
Rossi GC, Pasinetti GM, Scudeller L, Bianchi PE. Ocular surface disease and glaucoma: how to evaluate impact on quality of life. J Ocul Pharmacol Ther. 2013 May;29(4):390-4. doi: 10.1089/jop.2011.0159. Epub 2012 Dec 7.
Results Reference
result
PubMed Identifier
23335308
Citation
Rossi GC, Pasinetti GM, Scudeller L, Raimondi M, Lanteri S, Bianchi PE. Risk factors to develop ocular surface disease in treated glaucoma or ocular hypertension patients. Eur J Ophthalmol. 2013 May-Jun;23(3):296-302. doi: 10.5301/ejo.5000220. Epub 2012 Dec 17.
Results Reference
result
PubMed Identifier
31823206
Citation
Kallab M, Szegedi S, Hommer N, Stegmann H, Kaya S, Werkmeister RM, Schmidl D, Schmetterer L, Garhofer G. Correction to: Topical Low Dose Preservative-Free Hydrocortisone Reduces Signs and Symptoms in Patients with Chronic Dry Eye: A Randomized Clinical Trial. Adv Ther. 2020 Jan;37(1):342-343. doi: 10.1007/s12325-019-01190-3.
Results Reference
result
PubMed Identifier
34406502
Citation
Filippelli M, dell'Omo R, Gelso A, Rinaldi M, Bartollino S, Napolitano P, Russo A, Campagna G, Costagliola C. Effects of topical low-dose preservative-free hydrocortisone on intraocular pressure in patients affected by ocular surface disease with and without glaucoma. Graefes Arch Clin Exp Ophthalmol. 2022 Jan;260(1):247-253. doi: 10.1007/s00417-021-05345-3. Epub 2021 Aug 18.
Results Reference
derived
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Effects of Topical Low Dose Preservative-free Hydrocortisone on Intraocular Pressure
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