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Observational Study of How Patients Take Eye Drops
This study is currently recruiting participants.
Verified by Robin, Alan L., M.D., September 2008
First Received: September 9, 2008   No Changes Posted
Sponsors and Collaborators: Robin, Alan L., M.D.
Alcon Laboratories
Information provided by: Robin, Alan L., M.D.
ClinicalTrials.gov Identifier: NCT00750646
  Purpose

This study is interested in monitoring how patients take eye drops, both through video-recordings and adherence monitoring, as well as their perceptions about their eye medications; including the dosing schedules, instillation techniques and effect on their disease.


Condition Intervention
Glaucoma
Device: MEMS cap

Genetics Home Reference related topics: early-onset glaucoma
MedlinePlus related topics: Glaucoma
Drug Information available for: Tetrahydrozoline Tetrahydrozoline hydrochloride
U.S. FDA Resources
Study Type: Observational
Study Design: Cohort, Prospective
Official Title: The Relationship Between Glaucoma Medication Self-Efficacy, Outcome Expectations, Eye Drop Tech., Adherence and IOP.

Further study details as provided by Robin, Alan L., M.D.:

Primary Outcome Measures:
  • Medication adherence measured by MEMS caps [ Time Frame: 3 months ] [ Designated as safety issue: No ]
  • Eye drop technique measured by video evaluation [ Time Frame: 1 time observation ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Medication adherence measured by self-report [ Time Frame: 3 months ] [ Designated as safety issue: No ]
  • Severity of VF damage [ Time Frame: 1 test date ] [ Designated as safety issue: No ]
  • Intraocular pressure readings [ Time Frame: 3 months ] [ Designated as safety issue: No ]

Biospecimen Retention:   None Retained

Biospecimen Description:

Estimated Enrollment: 220
Study Start Date: September 2008
Estimated Study Completion Date: August 2009
Estimated Primary Completion Date: March 2009 (Final data collection date for primary outcome measure)
Groups/Cohorts Assigned Interventions
A
Subject's adherence to prescribed therapy will be monitored with an electronic compliance device.
Device: MEMS cap
The Medication Event Monitoring System will be used to assess the level of subject adherence to recommended topical eye drop therapy.

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population

Subjects will be enrolled for a single site, private practice.

Criteria

Inclusion Criteria:

  • >18 year old
  • currently taking 1 or more hypotensive topical eye drops takes drops in the right eye for more than 6 months expect to continue drop use for the next 3 months
  • subjects instill their own eye drops
  • subject is able to take HVF tests
  • subject will expect to complete the 3 months enrollment period

Exclusion Criteria:

  • unable/unwilling to instill own medications
  • eye drops are discontinued
  • unable to take HVF test
  • unable to complete follow-up
  • investigators discontinue subject for safety reasons
  • not using drops in left eye
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00750646

Contacts
Contact: Jennifer L Stone, OD 410 377 2422 jstone@glacuomaexpert.com
Contact: Colleen K Protzko 4103772422 cprotzko@glaucomaexpert.com

Locations
United States, Maryland
Glaucoma Specialists Recruiting
Baltimore, Maryland, United States, 21209
Contact: Colleen K Protzko     410-377-2422     cprotzko@glaucomaexpert.com    
Contact: Millie Brummett     4103772422        
Principal Investigator: Jennifer L Stone, OD            
Sub-Investigator: Alan L Robin, MD            
Sponsors and Collaborators
Robin, Alan L., M.D.
Alcon Laboratories
Investigators
Principal Investigator: Jennifer L Stone, OD Glaucoma Experts
Principal Investigator: Alan L Robin, MD Glaucoma Specialists
Study Director: Colleen K Protzko Glaucoma Specialists
  More Information

No publications provided

Responsible Party: Glaucoma Specialists ( Alan L. Robin )
Study ID Numbers: SI-08-54
Study First Received: September 9, 2008
Last Updated: September 9, 2008
ClinicalTrials.gov Identifier: NCT00750646     History of Changes
Health Authority: United States: Institutional Review Board

Keywords provided by Robin, Alan L., M.D.:
compliance
eye drop administration
MEMS
adherence

Study placed in the following topic categories:
Pseudoephedrine
Eye Diseases
Tetrahydrozoline
Cardiovascular Agents
Nasal Decongestants
Oxymetazoline
Glaucoma
Phenylephrine
Vasoconstrictor Agents
Ephedrine
Peripheral Nervous System Agents
Ocular Hypertension
Hypertension

Additional relevant MeSH terms:
Respiratory System Agents
Sympathomimetics
Eye Diseases
Physiological Effects of Drugs
Tetrahydrozoline
Cardiovascular Agents
Pharmacologic Actions
Nasal Decongestants
Glaucoma
Autonomic Agents
Therapeutic Uses
Vasoconstrictor Agents
Peripheral Nervous System Agents
Ocular Hypertension

ClinicalTrials.gov processed this record on May 07, 2009