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Main
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Note: This record shows only the 20 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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17 October 2012 |
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Main ID: |
NCT01477996 |
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Date of registration:
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08/08/2011 |
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Primary sponsor: |
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Public title:
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Pain After Intravitreal Therapy
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Scientific title:
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Date of first enrolment:
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August 2011 |
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Target sample size:
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200 |
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Recruitment status: |
Recruiting |
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URL:
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http://clinicaltrials.gov/show/NCT01477996 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment
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Countries of recruitment
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Austria
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Contacts
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Name:
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Christiane I Falkner-Radler, MD |
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Address:
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Telephone:
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0043711654607 |
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Email:
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christiane.falkner-radler@wienkav.at |
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Affiliation:
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Name:
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Christiane I Falkner-Radler, MD |
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Address:
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Telephone:
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0043711654607 |
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Email:
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christiane.falkner-radler@wienkav.at |
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Affiliation:
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Name:
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Christiane I Falkner-Radler, MD |
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Address:
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Telephone:
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Email:
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Affiliation:
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The Ludwig Boltzmann Institute of Retinology and Biomicroscopic Laser Surgery |
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Name:
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Susanne Binder, MD |
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Address:
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Telephone:
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Email:
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Affiliation:
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The Ludwig Boltzmann Institute of Retinology and Biomicroscopic Laser Surgery |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- vitrearetinal disease including age-related macular degeneration,
- clinical significant macular edema due to diabetic retinopathy or other vascular
disorders
- treatment with intravitreal therapy
Exclusion Criteria:
- missing informed consent
- age under 50 years
Age minimum:
51 Years
Age maximum:
N/A
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Pain
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Intervention(s)
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Procedure: 27-gauge
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Procedure: 30-gauge
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Primary Outcome(s)
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Visual Analoge Scale
[Time Frame: 1 day, after the intravitreal therapy (IVT)]
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Secondary Outcome(s)
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Baker scale
[Time Frame: 1 day, after the intravitreal therapy (IVT)]
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patients demographic data
[Time Frame: 1 day, record of patients data before or after intravitreal therapy (IVT)]
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Secondary ID(s)
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FR-7-CI-2011
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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