Ranibizumab in Idiopathic Parafoveal Telangiectasia (RIPT) Trial
Part of paid clinical trials in Baltimore, Maryland.
- Sponsor
- Johns Hopkins University
- Study ID
- NCT00378196
- Phase
- PHASE1
- Status
- Completed
Conditions
- Telangiectasia
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Ranibizumab — DRUG0.3 mg/0.05 ml dose
- Ranibizumab — DRUG0.5 mg/0.05 ml dose
Study Details
This research is being done to look at the effects of an experimental drug, ranibizumab, for the treatment of a condition called "idiopathic parafoveal telangiectasia" or IPT. IPT is caused by swelling in the retina (the light sensitive tissue in the back of the eye) due to leaky blood vessels in this area. Swelling in the retina can lead to blurry vision.
Key Dates
- First listed
- Sep 19, 2006
- Start date
- Sep 30, 2006
- Status verified
- Nov 2012
- Primary completion
- Sep 30, 2007
- Completion
- Dec 31, 2008
Study Design
- Enrollment
- 10 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: A0.3 mg/0.05 ml dose of ranibizumab
- Experimental: B0.5 mg /0.05 ml dose of ranibizumab
Primary Outcome Measure
Proportion of subjects with improvement of 15 or more letters of best corrected visual acuity from baseline to 3 months on an Early Treatment Diabetic Retinopathy visual acuity chart measured at 4 meters [ Time Frame: 3 months ]
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| The Wilmer Eye Institute at Johns Hopkins | Baltimore | Maryland | 21287 | - |
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