A dose of 0.5 g of a negative oral contrast agent for labelling the bo
wel, was given to 40 patients in a clinical trial. Oral magnetic parti
cles (OMP) consist of crystals of iron oxide with superparamagnetic pr
operties, and are administered in 800 ml of a viscous suspension in or
der to obtain a uniform distribution. The aim of the study was to iden
tify any adverse effects up to 1 week following ingestion, as well as
the contrast distribution and effect, together with the induction of a
rtifacts. A comparison of diagnostic value of the pre and postcontrast
ingestion series was also performed. Vomiting followed ingestion in a
single patient already nauseated and was the only adverse effect. Goo
d contrast distribution and effect with no artifacts were present. The
diagnostic information was greatly improved after OMP ingestion, and
the diagnosis would not have been possible without the use of the cont
rast agent in 41% of the examinations.