Patient Consent

For all studies involving patients, the patients must be informed about the study objectives and any other consequences of the study on their health. Any information that reveals the identity of the patient such as names, photos or any other information must not be disclosed unless it is required for scientific purposes. The ethical approval number assigned to human studies must be disclosed in the methodology section of the article. All clinical trails    must be registered to clinical trial registries: http://www.ctri.in/ http://www.actr.org.au/ http://www.clinicaltrials.gov/ http://isrctn.org/ http://www.trialregister.nl/ http://www.umin.ac.jp/ctr