Implication of CD35, CD21 and CD55 in Exudative Age-related Macular Degeneration
The recruitment status of this study is unknown because the information has not been verified recently.
Verified August 2010 by Rudolf Foundation Clinic.
Recruitment status was Active, not recruiting
Recruitment status was Active, not recruiting
Sponsor:
Rudolf Foundation Clinic
Information provided by:
Rudolf Foundation Clinic
ClinicalTrials.gov Identifier:
NCT01174407
First received: November 19, 2008
Last updated: August 2, 2010
Last verified: August 2010
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Purpose
The purpose of this study is to determine a possible implication of CD21, CD35 and CD55 in the pathogenesis of age-related macular degeneration. The aim is to asses a difference in expression rates of these factors on AMD-patients and a healthy control group.
| Condition | Intervention |
|---|---|
|
Age-Related Macular Degeneration |
Other: cd 35, cd21, cd55 |
| Study Type: | Observational |
| Study Design: | Observational Model: Case Control Time Perspective: Prospective |
| Official Title: | Is CD35, CD21 and CD55 Associated With Exudative Age-related Macular Degeneration |
Resource links provided by NLM:
Genetics Home Reference related topics:
age-related macular degeneration
X-linked juvenile retinoschisis
MedlinePlus related topics:
Macular Degeneration
U.S. FDA Resources
Further study details as provided by Rudolf Foundation Clinic:
Primary Outcome Measures:
- determine a possible implication of CD21, CD35 and CD55 in the pathogenesis of age-related macular degeneration [ Time Frame: 1 day ] [ Designated as safety issue: No ]
Secondary Outcome Measures:
- expression rates of on AMD-patients and a healthy control group [ Time Frame: 1 year ] [ Designated as safety issue: No ]
| Estimated Enrollment: | 120 |
| Study Start Date: | September 2008 |
| Estimated Study Completion Date: | August 2010 |
| Estimated Primary Completion Date: | December 2009 (Final data collection date for primary outcome measure) |
| Groups/Cohorts | Assigned Interventions |
|---|---|
| cd35 |
Other: cd 35, cd21, cd55
Blood drawing/ 10ml/ once- duration of 1 day of full examination of the patient
|
Eligibility| Ages Eligible for Study: | 55 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
| Sampling Method: | Non-Probability Sample |
Study Population
patients with exudative age-related macular degeneration, over 55
Criteria
Inclusion Criteria:
- Man and women over 18 years old
- Filled out informed consent
- Diagnosis of non-exudative/ exudative age related macular degeneneration
Exclusion Criteria:
- Inherited retinal diseases
- Other acquired retinal/ macular
- Missing informed consent
Contacts and Locations
More Information
No publications provided by Rudolf Foundation Clinic
Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
| Responsible Party: | Prof. Dr. Susanne Binder, Rudolf Foundation Clinic |
| ClinicalTrials.gov Identifier: | NCT01174407 History of Changes |
| Other Study ID Numbers: | EK08010-VK |
| Study First Received: | November 19, 2008 |
| Last Updated: | August 2, 2010 |
| Health Authority: | Austria: Ethikkommission |
Additional relevant MeSH terms:
|
Macular Degeneration Wet Macular Degeneration Retinal Degeneration Retinal Diseases Eye Diseases |
ClinicalTrials.gov processed this record on May 19, 2013