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Efficient Study of ACULAR in Inhibiting Proliferative Retinopathy in Prematurity (ROP)
This study is enrolling participants by invitation only.
First Received: March 5, 2008   Last Updated: March 12, 2008   History of Changes
Sponsor: University of South Alabama
Information provided by: University of South Alabama
ClinicalTrials.gov Identifier: NCT00634972
  Purpose

The purpose of this study is to test whether ACULAR, a nonsteroidal anti-inflammatory eye drop medication, can prevent the development of retinopathy of prematurity (ROP) and/ or decrease its severity.In this study ACULAR will be compared to a placebo (artificial tear).

The hypothesis would be that ACULAR treatment will decrease the incidence of moderate to severe ROP (grade II and above)by 50%.


Condition Intervention Phase
Retinopathy of Prematurity
Retinal Detachment
Blindness
Drug: ACULAR
Drug: REFRESH TEARS
Drug: placebo
Phase IV

Study Type: Interventional
Study Design: Prevention, Randomized, Double Blind (Subject, Caregiver, Investigator), Placebo Control, Factorial Assignment, Safety/Efficacy Study
Official Title: Topical Application of ACULAR a Randomized, Vehicle Controlled Clinical Trial: Efficiency in Inhibiting Proliferative Retinopathy of Prematurity

Resource links provided by NLM:


Further study details as provided by University of South Alabama:

Primary Outcome Measures:
  • Efficacy of ACULAR compared to placebo in inhibiting the development of retinopahty of prematurity in a high risk very immature preterm group of infants [ Time Frame: 3-4 years ] [ Designated as safety issue: Yes ]

Estimated Enrollment: 200
Study Start Date: November 2005
Estimated Study Completion Date: December 2009
Estimated Primary Completion Date: August 2009 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
1: Experimental Drug: ACULAR
infants enrolled in the study will receive 1 drop of the ROP Study drug in each eye 3 times a day (every 8 hours.
Drug: REFRESH TEARS
infants enrolled in the study will receive 1 drop of the ROP Study drug in each eye 3 times a day (every 8 hours.
2: Placebo Comparator Drug: placebo

Detailed Description:

Each year ROP affects an estimated 14,000-16,000 premature, low birth weight infants in the United States and thousands more worldwide, making it a leading cause of vision loss in children. Of these cases, approximately 1500 infants will develop severe ROP that requires surgical treatment. Despite those treatment, about 400-600 infants with severe ROP still become legally blind each year.

ACULAR® (Ketorolac eye drop) is a member of nonsteroidal anti-inflammatory drugs (NSAIDs) available for toipcal ocular use. ACULAR acts as prostaglandin inhibitor and as such decrease prostaglandin E2 production. An increase in prostaglandin production has been associated with various inflammatory eye disease.For instance ACULAR has been shown to be effective in preventing the post cataract surgery inflammation that result in macular edema in adults. Activation of the prostaglandin cascade has been demonstrated in animal models of ROP. A previous non randomized study using ACULAR for ROP prevention has shown a possible beneficial effect and no observed adverse effect. To clearly demonstrated and confirm this finding a randomized study is thus necessary before one can advocate its use for prevention of ROP.The medication is FDA approved in pediatrics for allergic conjunctivitis and post surgical ocular inflammation.

  Eligibility

Ages Eligible for Study:   up to 15 Days
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • All preterm infants of gestational age less or equal to 28 weeks completed gestational age and 10 to 15 days of postnatal age admitted to our regional NICU
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00634972

Locations
United States, Alabama
Division of Neonatology, Children's & Women's Hospital, University of South Alabama
Mobile, Alabama, United States, 36604-3391
Sponsors and Collaborators
University of South Alabama
Investigators
Principal Investigator: Fabien G Eyal, M.D. University Of South Alabama, Children's & Women's Hospital
  More Information

No publications provided

Responsible Party: University of South Alabama, Children's and Women' s Hospital ( Fabien G. Eyal, M.D. )
Study ID Numbers: 05-156, 05-156
Study First Received: March 5, 2008
Last Updated: March 12, 2008
ClinicalTrials.gov Identifier: NCT00634972     History of Changes
Health Authority: United States: Institutional Review Board

Keywords provided by University of South Alabama:
Retinopathy of Prematurity
Premature Infants
ACULAR
Refresh Tears

Additional relevant MeSH terms:
Anti-Inflammatory Agents
Sensation Disorders
Vision Disorders
Molecular Mechanisms of Pharmacological Action
Ketorolac
Physiological Effects of Drugs
Signs and Symptoms
Sensory System Agents
Therapeutic Uses
Infant, Newborn, Diseases
Anti-Inflammatory Agents, Non-Steroidal
Analgesics
Retinal Diseases
Eye Diseases
Nervous System Diseases
Cyclooxygenase Inhibitors
Enzyme Inhibitors
Infant, Premature, Diseases
Blindness
Pharmacologic Actions
Retinal Detachment
Analgesics, Non-Narcotic
Neurologic Manifestations
Retinopathy of Prematurity
Peripheral Nervous System Agents
Ketorolac Tromethamine
Antirheumatic Agents
Central Nervous System Agents

ClinicalTrials.gov processed this record on February 08, 2010