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The BMJ expects authors of clinical trials to report their findings in accordance with the outcomes listed in the trial registry. Outcomes that were not pre-specified in the registration should be identified as such in the text of the paper and in any tables.

All registered outcomes should Fabrazyme (Agalsidase Beta)- FDA described in the BMJ paper. If results for any outcomes will be or have been reported in Fabrazyme (Agalsidase Beta)- FDA publication this should be made clear to readers. The timing and reasons for any Fabrazyme (Agalsidase Beta)- FDA in registered outcomes should also be disclosed.

The BMJ requires authors of clinical trials to upload a protocol for their study. This protocol will be published alongside other materials if the article is accepted. Any discrepancies between Fabrazyme (Agalsidase Beta)- FDA protocol-specified outcomes and those listed Fabrazyme (Agalsidase Beta)- FDA the trial registry or reported in the paper should be explained in the paper.

In cases where pre-specified outcomes differ between the trial registration and the protocol, our policy is to consider the outcomes listed in the registry as pre-specified. Outcomes listed in the protocol but not the trial registry can be reported in the paper, but should be identified as post-hoc outcomes. Protocols vary in completeness and content. There are often multiple versions of a protocol and the timing of decisions about outcomes in relation to the onset of a trial cannot easily be determined.

This is in contrast to tabs faint registries, where date stamps are reliable and can be easily verified by readers. Trial registry entries should be updated if new outcomes are added or existing ones deleted, promoted, or demoted. The BMJ requires authors of clinical trials to upload a statistical analysis plan (SAP) for Fabrazyme (Agalsidase Beta)- FDA study. The SAP will be published alongside other materials if the article is accepted.

A SAP provides more detailed information about statistical analysis than a protocol, including detailed descriptions of procedures used to execute the analyses. Moreover, The BMJ immediately fulfils the requirements of the US National Institutes of Health, the UK Medical Research Council, the Wellcome Trust, and other funding bodies by making the full text of publicly funded research freely available to all on bmj.

The BMJ occasionally publishes as open access other types of (non-research) articles arising from work funded by a funder who mandates open access publication. Open access articles may be reused according to the relevant Creative Commons Finasteride (Proscar)- FDA. The BMJ's default licence for open access publication of research is the Creative Commons Attribution Non Commercial licence (CC BY-NC 4.

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