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Assessment of Inflammatory Biomarkers Expressed in a Sjogren's Population: Effect of a Topical Steroid Intervention (JADE2)

This study is currently recruiting participants.
Verified by Alcon Research, February 2008

Sponsored by: Alcon Research
Information provided by: Alcon Research
ClinicalTrials.gov Identifier: NCT00631358
  Purpose

The primary purpose of this study is to quantify the change in expression of biomarkers on the ocular surface of Sjogren's Syndrome participants after treatment with Maxidex.


Condition Intervention Phase
Sjogren's Syndrome
Drug: 0.1% Dexamethasone (Maxidex)
Phase IV

MedlinePlus related topics:   Sjogren's Syndrome   

Drug Information available for:   Dexamethasone    Dexamethasone acetate    Dexamethasone Sodium Phosphate    Doxiproct plus   

U.S. FDA Resources

Study Type:   Interventional
Study Design:   Treatment, Non-Randomized, Open Label, Single Group Assignment

Further study details as provided by Alcon Research:

Primary Outcome Measures:
  • Change in levels of biomarkers after dosing with Maxidex [ Time Frame: After 2 weeks on treatment ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Correlation between biomarker expression, and corneal staining, tear film break up time and ocular symptoms [ Time Frame: After 2 weeks of treatment ] [ Designated as safety issue: No ]

Estimated Enrollment:   90
Study Start Date:   February 2008
Estimated Primary Completion Date:   June 2008 (Final data collection date for primary outcome measure)

Arms Assigned Interventions
1: No Intervention
No treatment
2: Active Comparator
Treatment with Maxidex
Drug: 0.1% Dexamethasone (Maxidex)
Anti-inflammatory Agent

  Eligibility
Ages Eligible for Study:   17 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes

Criteria

Inclusion Criteria of Sjorgren's Population:

Inclusion Criteria:

  • 17 years or older
  • LogMar visual acuity of 0.6 or better
  • Ocular inflammation associated with Sjogren's Syndrome

Exclusion Criteria:

  • Has had an adverse reaction to either topical of systemic steroids in the past
  • Has diabetes (type 1 or 2)
  • Has glaucoma or evidence of ocular hypertension in either eye or treatment of either within six months of Visit 1
  • Has worn contact lenses within one week prior to Visit 1
  • Has received ocular prescription therapy in the last 30 days
  • Has active ocular infections or inflammation not associated with Sjogren's Syndrome.
  • Has any finding in the vitreous, macula, retina or choroid that show signs of inflammation and/or any structural change that in the opinion of the investigator is considered abnormal or unstable for that participant
  Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00631358

Contacts
Contact: Ravaughn K Williams, OD,MS     817-302-5605    

Locations
Canada
Waterloo     Recruiting
      Waterloo, Canada
Toronto     Recruiting
      Toronto, Canada

Sponsors and Collaborators
Alcon Research
  More Information


Responsible Party:   Alcon ( Ravaughn Williams, OD, MS )
Study ID Numbers:   ORE 14351
First Received:   February 29, 2008
Last Updated:   February 29, 2008
ClinicalTrials.gov Identifier:   NCT00631358
Health Authority:   Canada: Health Canada;   Canada: Institutional Ethics Committee

Keywords provided by Alcon Research:
Ocular inflammation  

Study placed in the following topic categories:
Dexamethasone
Mouth Diseases
Autoimmune Diseases
Eye Diseases
Joint Diseases
Arthritis, Rheumatoid
Lacrimal Apparatus Diseases
Dry Eye Syndromes
Rheumatic Diseases
Xerostomia
Inflammation
Musculoskeletal Diseases
Arthritis
Connective Tissue Diseases
Sjogren's Syndrome
Stomatognathic Diseases
Salivary Gland Diseases
Dexamethasone acetate

Additional relevant MeSH terms:
Anti-Inflammatory Agents
Disease
Antineoplastic Agents, Hormonal
Immune System Diseases
Antineoplastic Agents
Physiological Effects of Drugs
Hormones, Hormone Substitutes, and Hormone Antagonists
Gastrointestinal Agents
Antiemetics
Hormones
Glucocorticoids
Pharmacologic Actions
Pathologic Processes
Autonomic Agents
Syndrome
Therapeutic Uses
Peripheral Nervous System Agents
Central Nervous System Agents

ClinicalTrials.gov processed this record on October 31, 2008




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