Table 1. Selected clinicals trials to date.
Drug | Treatment | Outcome | Patients | |
---|---|---|---|---|
Rogers et al, 1993207 | Indomethacin | 6 months | Positive effects after marked attrition | 41 AD |
De Jong et al, 2008208 | Indomethacin | 1 year | Neutral to positive effects after marked attrition | 51 mild to moderate AD |
Aisen et al, 2000211 | Prednisone | 1 year | Neutral to negative effects | 138 AD |
Aisen et al, 2003209 | Naproxen, rofecoxib | 1 year | Neutral to negative effects | 351 mild-to-moderate AD |
Aisen et al, 2002228 | Nimesulide | 3 months | Neutral effects | 40 AD |
Reines et al, 2004210 | Rofecoxib | 1 year | Neutral to negative effects | 692 mild-to-moderate AD |
Thal et al, 2005229 | Rofecoxib | 3.5 years, preventive | Neutral to negative effects on conversion to AD | 1457 mild cognitive impairment |
Van Gool et al, 2001212 | Hydroxychloro quine | 18 months | Neutral effects | 168 mild AD |
ADAPT Research | Celecoxib | 2 years, preventive | Neutral to negative effects | 2528 normal with family |
Research Group, 2007, 2008218,230 | effects | with family history of AD | ||
ADAPT Research Group, 2007, 2008218,230 | Naproxen | 2 years, preventive | Neutral to negative effects | 2528 normal wit family history of AD |
Simons et al, 2002213 | Simvastatin | 26 weeks | No effects on CSF Aβ | 44 AD |
Sparks et al, 2005214 | Atorvastin | 72 weeks | Neutral effects | 640 mild to moderate AD |
Feldman et al, 2010215 | Atorvastatin | 1 year | Neutral to positive effects | 67 mild AD |
Gold et al, 2007217 | Rosiglitazone | 24 weeks | Neutral effects | 693 mild to moderate AD |
Breitner et al, 2011219 | Naproxen | 4 years, preventive | Neutral to positive effects | 2528 normal with family history of AD |
Breitner et al, 2011219 | Celecoxib | 4 years, preventive | neutral to negative effects | 2528 normal with family history of AD |
We searched PubMed for randomised controlled trials published in English. The table provides a list of trial results that have had a notable influence on the field, in our view, and is not an exhaustive list of studies. Priority was given to trials with sufficient numbers of participants, definition of clinical outcomes, and specification of design methodology to allow firm conclusions to be drawn (including inference of uncertainty). Two older trials were included because of their influence on later work, despite the fact that they failed to meet the foregoing criteria.