Version 1.3; 18/05/2012 Consent Form Genomic and expression profiling of brain tumors Project ref 08/0077 Please initial box I confirm that I have read and understood the information sheet dated May 2012 (version 1.6) for the above study and have had the opportunity to ask questions. I confirm that I have had sufficient time to consider whether or not want to be included in the study I understand that only tissue appropriate for the treatment of my condition or for establishing a diagnosis will be removed during surgery. I give my permission that tissue which is surplus to requirements for diagnostic tests and that would normally be disposed of may be used for research purposes. Please I understand that future research using my sample I give may include contact genetic research aimed at understanding genetic influences on diseases, me however the results of these investigations are unlikely to have any implications for me personally. If they do, I wish / do not wish to be contacted (please tick appropriate box). Please DO NOT contact me I understand that in agreeing to this use of tissue I am donating it indefinitely to the NHNN/IoN. The NHNN/IoN will be responsible for its storage for its use in future research projects and its eventual disposal. I give my permission that, with the approval of my consultant, clinical data relevant to the approved project may be extracted from my case notes and given the research team for analysis. This data will be anonymised prior to its release I understand that I will not benefit financially from the donation of the tissue I understand that my participation is voluntary and that I am free to withdraw at any time, without giving any reason, without my medical care or legal rights being affected I agree to take part in this study ________________________ Name of Patient (Patient/Guardian delete as appropriate) ___________________ Date _____________________ Signed ________________________ Name of Person taking consent ___________________ Date _____________________ Signed Page 1 of 3 Version 1.3; 18/05/2012 Further information and contact details For general information about research you may find the following websites helpful: - http://www.nres.npsa.nhs.uk/ - http://www.brt.org.uk/ For specific information about this study or advice as to whether to participate please contact: - Professor Sebastian Brandner (Neuropathology) Tel 020 3448 4435 - Mr Neil Kitchen (Neurosurgery) Tel 020 7829 8714 Comments or concerns during the study If you have any comments or concerns you may discuss these with the investigator. If you wish to go further and complain about any aspect of the way you have been approached or treated during the course of the study, you should write or get in touch with the Complaints Manager, UCL hospitals. Please quote the UCLH project number at the top this consent form One signed original to be kept on file by the researcher One copy to be given to patient (with a copy of the Patient Information) One copy to be kept in the hospital notes Page 2 of 3 Version 1.3; 18/05/2012 THE DATA AND PROTECTION ACT 1998 Data collection and medical research In accordance to the requirements of the Data Protection Act 1998 we wish to inform you that we hold information relating to your treatment at this hospital on a confidential secure database for the purposes of providing health care and undertaking medical research and statistical analysis. You have the right to request that information stored about you is removed from our databases. Please let us know if this is the case by ticking the box below. I, …………………………………….. date: ……………… do/do not * consent to having my personal data stored on Institute of Neurology database. * delete as appropriate . Signed: …………………………………. Witness: ………………………………….. Date: Print Name: …………………………. Print Name: ………………………… ………………………………….. Investigator’s Statement: I have explained the nature, demands and foreseeable risks of the above research to the subject: Name: ……………………………………………………….. Signature: …………………………………………………. Date: ……………. IMPORTANT: One signed original to be kept on file by the researcher One copy to be given to patient (with a copy of the Patient Information) One copy to be kept in the hospital notes Page 3 of 3