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Inhaled Corticosteroids: Effect on Intraocular Pressure in Patients With Controlled Glaucoma

The Effect of Inhaled Corticosteroids on Intraocular Pressure in Patients With Ocular Hypertension or Controlled Glaucoma.

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02338362
Enrollment
22
Registered
2015-01-14
Start date
2014-09-30
Completion date
2015-02-28
Last updated
2019-05-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Glaucoma, Open-Angle, Ocular Hypertension

Keywords

Corticosteroids, Bronchodilator Agents, Intraocular Pressure

Brief summary

The purpose of this study is to determine whether a commonly prescribed orally inhaled corticosteroid treatment will induce a clinically meaningful elevation in intraocular pressure, when administered to patients with ocular hypertension (OHT) or open-angle glaucoma (OAG). Based on the response to high-dose corticosteroids, this patient group is more likely than the normal population to demonstrate this adverse effect.

Detailed description

Systemic and topical ophthalmic steroids have long been associated with ocular effects, such as glaucoma or cataracts.\[Alfano JE; Bernstein HN et al. 1962; Bernstein HN et al. 1963; Becker B and Mills DW in Arch Ophthalm 1963; Becker B and Mills DW in JAMA 1963; Armaly MF 1963 (1); Armaly MF 1963 (2); and Buckley RJ\] Periocular steroid injections \[Herschler J; Kalina RE\] and steroids applied to periocular skin \[Aggarwal RK et al.\] have also been reported to increase intraocular pressure (IOP) and raised IOP is the major risk factor for glaucoma. Ocular hypertension (OHT) is defined as an IOP above 21mmHg in one or both eyes without detectable glaucomatous damage. Primary open-angle glaucoma (POAG) is a chronic and progressive optic neuropathy of unknown etiology characterized by disc cupping, and often associated with visual field defects and elevated IOP. This disease is one of the leading causes of blindness worldwide.\[Kwon YH et al.\] Approximately 18% to 36% of the general population are corticosteroid responders. This response is increased to 46% to 92% in patients with POAG.\[Tripathi RC et al.\] Asthma is the most common chronic respiratory illness in Canada, affecting approximately 10% of the population. For the majority of these patients, long-term inhaled corticosteroids (ICS) are standard of care to prevent acute asthma exacerbations.\[Kim H and Mazza J\] Although the systemic absorption of inhaled and nasal steroids has been established, the clinically relevant ocular side effects are poorly defined. \[Cave A et al.; Allen DB et al.\] A large prospective study in 1995 by Samiy et al reported no statistically significant increase of IOP in 187 patients without glaucoma taking inhaled steroids for various pulmonary conditions.\[Samiy N et al.\] However, six cases of increased IOP associated with combined nasal and inhaled steroid use in non-glaucomatous patients have been reported. \[Dreyer EB; Desnoeck M et al.; Opatowsky I et al.\] A large case-control study in 1997 suggested that current users of high doses of ICS prescribed regularly for 3 or more months were at increased risk of OHT or OAG (OR 1.44; 95% CI 1.01-2.06).\[Garbe E et al.\] In contrast, Gozalez et al. conducted a nested case-control study in 2010 with Quebec data which showed current and continuous use of ICS did not result in increased risk of glaucoma or raised IOP requiring treatment.\[Gonzalez AV et al.\] Similarly, Duh et al. reported no association between inhaled budesonide daily therapy and increased IOP in 1255 asthmatic patients.\[Duh MS et al.\] Further, a prospective population-based cohort study published in 2012 suggested no association between the development of OAG and ICS in the elderly.\[Marcus MW et al.\] In 2013, our group published a randomized double-masked controlled trial that showed no evidence of IOP elevation after 6 weeks use of beclomethasone nasal spray in 19 patients with OHT and POAG.\[Yuen D et al.\] The purpose of the current study protocol would be to extend the study to investigate ICS in the same patient population. To date, the effect of inhaled corticosteroids in those with pre-existing OHT or POAG remains uncertain. Considering the large number of patients on inhaled steroids, investigating the use of inhaled steroid in glaucoma patients could have significant clinical impact. This study was designed to evaluate the effect of inhaled fluticasone propionate on intraocular pressure (IOP) in patients with OHT or controlled open-angle glaucoma (OAG). Patient randomization was performed by an independent Research Coordinator in a separate physical space and kept sealed from the principal study investigators, who assessed and recorded outcome measures, until the completion of study data collection. IOP was measured in a masked fashion, using a second observer to record values. Two measurements within 1 mmHg were averaged for each data point. With a sample size of 8 patients per interventional arm, the study is powered at 0.80 to detect an elevation of 3.2 mmHg (≥20%) from mean, assuming a standard deviation of 2.5 mmHg. Baseline data will be compared between groups using the student's t test and Fisher exact test. A 2-sided p value of \<0.05 will be considered statistically significant. The primary outcome measure (mean IOP) will be assessed using a 1-sided Student t test.

Interventions

DRUGFluticasone propionate inhaler

fluticasone propionate 250 µg metered-dose inhaler

DRUGSaline placebo inhaler

saline metered dose inhaler

Sponsors

University Health Network, Toronto
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

* Age 18 to 85 years, inclusive * Mild-moderate open-angle glaucoma/ocular hypertension with cup:disc ratio \<0.85 vertically and humphrey visual field mean deviation \>-12.00 (BOTH EYES must meet this criteria for patient to be included) * Glaucoma well-controlled, defined by IOP \< 21 mmHg and at target with no visual field/disc progression for at least 6 months (BOTH EYES must meet this criteria for patient to be included)

Exclusion criteria

* Any form of steroid medication use within the prior 6 weeks * Any previous intra-ocular surgery or refractive surgery in the study eye * no light perception (i.e. blindness) in either eye * unwilling/unable to give consent * unwilling to accept randomization * patient potentially unavailable for follow-up visits

Design outcomes

Primary

MeasureTime frameDescription
Mean Intraocular Pressureweek 6Masked assessment of intraocular pressure using goldmann application tonometry. Mean of 2 measurements within 1 mmHg will be recorded.

Secondary

MeasureTime frameDescription
Mean Visual Acuityweek 6best corrected logMAR visual acuity for each eye. 20/20 vision corresponds with a logMAR score of 0, while negative logMAR scores indicate better than 20/20 vision, values \> 0.5 correspond with low vision, and values \> 1.3 correspond with blindness.
Side Effectsfrom baseline to week 6subjective (reported) and objective (slit lamp examination) side-effects attributable to study medications
Intraocular Pressure Elevation >20% From Baselinewithin 6-week observation periodParticipants with 2 consecutive intraocular pressure measurements exceeding 20% increase from baseline were discontinued from study.
AdherenceCompletion of study, up to 6 weeksAdherence was calculated from self-reported study diaries and correlated to a counter that measured number of inhaled puffs built into the placebo metered-dose inhalers

Participant flow

Recruitment details

1,960 records of glaucoma patients with scheduled visits in a university-based glaucoma clinic were screened between August 1, 2014 and November 7, 2014.

Pre-assignment details

22 consented to participate and 20 completed the study.

Participants by arm

ArmCount
Fluticasone
participants will be asked to use fluticasone propionate 250 µg metered-dose inhaler 1 puff twice-daily for 6 weeks.
10
Saline Placebo
participants will be asked to use a saline placebo metered-dose inhaler 1 puff twice-daily for 6 weeks.
10
Total20

Withdrawals & dropouts

PeriodReasonFG000FG001
Overall StudyWithdrawal by Subject11

Baseline characteristics

CharacteristicFluticasoneSaline PlaceboTotal
Age, Continuous65.7 years
STANDARD_DEVIATION 9
65.7 years
STANDARD_DEVIATION 11
65.7 years
STANDARD_DEVIATION 10
Diagnosis
Ocular Hypertension
1 participants4 participants5 participants
Diagnosis
Pigment Dispersion Glaucoma
3 participants1 participants4 participants
Diagnosis
Primary Open-Angle Glaucoma
6 participants4 participants10 participants
Diagnosis
Pseudoexfoliative Glaucoma
0 participants1 participants1 participants
Mean central corneal thickness553.1 micrometers
STANDARD_DEVIATION 31.7
549.1 micrometers
STANDARD_DEVIATION 30.8
551.1 micrometers
STANDARD_DEVIATION 31.25
Mean cup-disc ratio0.49 cup:disc ratio
STANDARD_DEVIATION 0.2
0.38 cup:disc ratio
STANDARD_DEVIATION 0.2
0.44 cup:disc ratio
STANDARD_DEVIATION 0.2
Mean intraocular pressure14.3 mmHg
STANDARD_DEVIATION 3
15.6 mmHg
STANDARD_DEVIATION 3.6
15.0 mmHg
STANDARD_DEVIATION 3.3
Mean logMAR visual acuity0.19 logMAR
STANDARD_DEVIATION 0.1
0.18 logMAR
STANDARD_DEVIATION 0.1
0.18 logMAR
STANDARD_DEVIATION 0.1
Mean number of ocular hypotensive medications1.3 medication classes
STANDARD_DEVIATION 0.7
1.3 medication classes
STANDARD_DEVIATION 1.4
1.3 medication classes
STANDARD_DEVIATION 1
Mean visual field mean deviation-0.72 decibels (dB)
STANDARD_DEVIATION 2.6
-1.13 decibels (dB)
STANDARD_DEVIATION 2.5
-0.92 decibels (dB)
STANDARD_DEVIATION 2.6
Prior laser trabeculoplasty1 participants0 participants1 participants
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Asian
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Black or African American
0 Participants0 Participants0 Participants
Race (NIH/OMB)
More than one race
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Unknown or Not Reported
10 Participants10 Participants20 Participants
Race (NIH/OMB)
White
0 Participants0 Participants0 Participants
Region of Enrollment
Canada
10 participants10 participants20 participants
Sex: Female, Male
Female
4 Participants4 Participants8 Participants
Sex: Female, Male
Male
6 Participants6 Participants12 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
— / —— / —
other
Total, other adverse events
2 / 102 / 10
serious
Total, serious adverse events
0 / 100 / 10

Outcome results

Primary

Mean Intraocular Pressure

Masked assessment of intraocular pressure using goldmann application tonometry. Mean of 2 measurements within 1 mmHg will be recorded.

Time frame: week 6

ArmMeasureValue (MEAN)Dispersion
FluticasoneMean Intraocular Pressure14.7 mmHgStandard Deviation 2.4
Saline PlaceboMean Intraocular Pressure14.8 mmHgStandard Deviation 3.8
Secondary

Adherence

Adherence was calculated from self-reported study diaries and correlated to a counter that measured number of inhaled puffs built into the placebo metered-dose inhalers

Time frame: Completion of study, up to 6 weeks

ArmMeasureValue (MEAN)Dispersion
FluticasoneAdherence93.6 percentage of required dosesStandard Deviation 7.1
Saline PlaceboAdherence96.1 percentage of required dosesStandard Deviation 4.4
Secondary

Intraocular Pressure Elevation >20% From Baseline

Participants with 2 consecutive intraocular pressure measurements exceeding 20% increase from baseline were discontinued from study.

Time frame: within 6-week observation period

ArmMeasureGroupValue (NUMBER)
FluticasoneIntraocular Pressure Elevation >20% From Baselineelevation >20%1 participants
FluticasoneIntraocular Pressure Elevation >20% From Baselineno elevation >20%9 participants
Saline PlaceboIntraocular Pressure Elevation >20% From Baselineelevation >20%0 participants
Saline PlaceboIntraocular Pressure Elevation >20% From Baselineno elevation >20%10 participants
Secondary

Mean Visual Acuity

best corrected logMAR visual acuity for each eye. 20/20 vision corresponds with a logMAR score of 0, while negative logMAR scores indicate better than 20/20 vision, values \> 0.5 correspond with low vision, and values \> 1.3 correspond with blindness.

Time frame: week 6

ArmMeasureValue (MEAN)Dispersion
FluticasoneMean Visual Acuity0.15 logMARStandard Deviation 0.12
Saline PlaceboMean Visual Acuity0.15 logMARStandard Deviation 0.08
Secondary

Side Effects

subjective (reported) and objective (slit lamp examination) side-effects attributable to study medications

Time frame: from baseline to week 6

ArmMeasureGroupValue (NUMBER)
FluticasoneSide Effectsthroat discomfort1 participants
FluticasoneSide Effectsdifficulty sleeping0 participants
FluticasoneSide Effectsheadache1 participants
FluticasoneSide Effectsno adverse effects8 participants
FluticasoneSide Effectslens opacity0 participants
Saline PlaceboSide Effectsno adverse effects8 participants
Saline PlaceboSide Effectslens opacity0 participants
Saline PlaceboSide Effectsthroat discomfort1 participants
Saline PlaceboSide Effectsheadache0 participants
Saline PlaceboSide Effectsdifficulty sleeping1 participants

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026