Welcome to the iNO Registry!
The Inhaled Nitric Oxide Registry is a European Collaboration which was established originally by a group of interested clinicians in 2006. It has been running in its current format since September 2009. Clinical and demographic information about children treated with iNO is collected in order to enhance clinical care and inform future research projects. The iNO Registry also aims to support education and training around the use of iNO and to promote greater collaboration between units using iNO.
In order to provide reassurance to potential collaborators and registered users of the Registry that due consideration has been given to security of the data held in the Registry, we have produced a quality assurance document to answer some of the questions you may have, please click on the link below
iNO Registry Quality Assurance Document v1.0
The iNO Registry is free to join and submit data. If you are interested in contributing to the Registry or require any further information then please contact our Database Administrator, Julie Wray, by clicking on the 'Contact us' menu option.
iNO Registry Data Forms
Please click on the link below to view a PDF of the data forms in the iNO Registry. iNO Registry Data Forms v2.0
Supported by an educational grant from: