Clinical Trials Directory

Trials / Terminated

TerminatedNCT03132272

Immunoadsorption for Treatment of Alzheimer's Disease

Efficacy of Immunoadsorption for Treatment of Persons With Alzheimer Dementia and Agonistic Autoantibodies Against alpha1A-adrenoceptor (IMAD)

Status
Terminated
Phase
N/A
Study type
Interventional
Enrollment
11 (actual)
Sponsor
University Medicine Greifswald · Academic / Other
Sex
All
Age
55 Years – 85 Years
Healthy volunteers
Not accepted

Summary

Efficacy of immunoadsorption for treatment of persons with Alzheimer dementia and agonistic autoantibodies against alpha1A-adrenoceptor.

Detailed description

The IMAD trial outlined aims to ascertain whether the positive effects of immunoadsorption (IA) on slowing down dementia progression, shown in a pilot trial, can be replicated in a slightly larger number of subjects and to comprehensively investigate the effects by a combination of brain and vessel imaging along with cognitive tests and further state-of-the-art cardiovascular, cerebrovascular and laboratory examinations. If the trial results underpin the hypothesis that IA effectively counteracts pathophysiological impairments and dementia-related cognitive decline, it may open up a new treatment approach against dementia, namely the reversal or avoidance of further vascular damage by the removal of agonistic autoantibodies (agAAB) in agAAB-positive persons. The aim of this study is (beside of safety) to demonstrate the stop of the vascular remodeling and cognition decline by immunoadsorption, a therapeutic method which is well established in cardiology and nephrology.

Conditions

Interventions

TypeNameDescription
DEVICEImmunoadsorption with GlobaffinImmunoadsorption for treatment of persons with Alzheimer Dementia

Timeline

Start date
2016-09-15
Primary completion
2020-10-12
Completion
2020-10-12
First posted
2017-04-27
Last updated
2021-03-09

Locations

1 site across 1 country: Germany

Source: ClinicalTrials.gov record NCT03132272. Inclusion in this directory is not an endorsement.