Organizations or clinical investigators with primary responsibility for initiating
and conducting clinical trials may submit trial data to ClinicalTrials.gov using
the Protocol Registration System (PRS). A trial must be approved by a human subject
review board and must conform to the regulations of the appropriate national health
authorities, in order to be registered.
For more information visit the
PRS Information Page
(http://prsinfo.clinicaltrials.gov).
Investigators or sponsors for trials which have been registered with ClinicalTrials.gov by another
individual or organization should contact that data provider directly with any questions
or concerns regarding the information posted on ClinicalTrials.gov.
