How to report your study results - ISRCTN registry

Описание: Add results to your ISRCTN study record using the form at https://www.isrctn.com/trial/report

The ISRCTN registry is a primary clinical trial registry recognised by the World Health Organization (WHO) and the International Committee of Medical Journal Editors (ICMJE). We register all clinical research studies (whether proposed, ongoing or completed), providing content validation and curation and the unique identification number necessary for publication. All study records in the database are freely accessible and searchable. For more information on ISRCTN please watch our video at    • ISRCTN - Register your clinical trial or s...   and for instructions on how to register your study please visit    • How to register your clinical trials and s...  .

From 2015 clinical trial registries have been expected to include information about results within 12 months of study completion. The results could be in the form of a link to a published article or a file containing the basic results without interpretation. If you have published your results in a peer-reviewed journal, you can use the form at https://www.isrctn.com/trial/report to provide a link to the publication on PubMed or its DOI.

If your study is complete but you have not published or are not planning to publish, you can also use this form to upload a basic results summary to your record. Disclosure of basic results in a registry should not preclude publication in a peer-reviewed journal. The basic results should include the following four sections only and not contain any interpretation of the results:

Participant Flow: A CONSORT flow diagram showing participants involved at each stage of the study (namely enrolment, intervention allocation, follow-up, and data analysis).
Baseline Characteristics: A table of the baseline demographic (age and gender) and clinical characteristics of the participants.
Outcome Measures: Tables of all of the primary and secondary outcome measures listed in the ISRCTN study record
Adverse Events: a table of all adverse events: anticipated and unanticipated, serious (life-threatening) and other, including a description of the adverse event and the number of participants affected. If there were no adverse events associated with your trial then please state “There were no adverse events associated with this trial.”
Once you have submitted the form the ISRCTN team will be alerted and an editor will update your study record and contact you by email to confirm.

For examples of basic results summaries, please see the following trial records: https://www.isrctn.com/ISRCTN70039829, https://www.isrctn.com/ISRCTN52695239 and https://www.isrctn.com/ISRCTN18436190.

To update any other fields in the study record please use the update request form at https://www.isrctn.com/trial/quickSta..., as demonstrated in our video at    • How to request an update to your study rec...  .


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