How to add a trial to the clinical trials wiki
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
This page provides directions and help for those who wish to add a trial to the clinical trial wiki. If you need more help contact the WikiDoc hotline at (617)-632-7590 or email us [2].
Complete Title of Study
In this section add the complete title as it appears at clinicaltrials.gov or as it appears in the main publication of the paper.
Study Acronym (The trial's abbreviation if there is one)
Often a trial will have an abbreviation, and this is called an acronym. Place that here. Also make sure that the acronym redirects to the page with the full name of the trial. To learn how to redirect a page click here.
Principal Investigator, Co-investigators, and Collaborating Institutions
If you know the name of the principal investigator (the person who led the trial) type it in here. This should be followed by the other investigators names. You can also copy and paste the authorship from the primary article reporting the results. A list of names cannot be copyrighted.
An example would be:
Principal Investigator: Tom Smith, M.D.
Co-investigators: Susan Harris, R.N.; Jane Doe, M.D.
Institutions: Duke University
Overview of Trial
None reported
Disease State(s) Studied (e.g. acute MI, breast cancer, etc.)
None reported
Study Phase (e.g. Phase I,II,III,IV) Study Phases are defined here
None reported
Study Design (e.g. multicenter, randomized, double blind, placebo controlled)
None reported
Study Arms and How They Were Treated (Intervention) (Explanation here)
None reported
Primary Pre-Specified Endpoint
None reported
Secondary Endpoints
None reported
Inclusion Criteria
None reported
Exclusion Criteria
None reported
Outcome: Primary endpoint (Report both relative risk reduction and absolute risk reduction as well as number needed to treat if available)
None reported
Outcome: Secondary endpoint (Report both relative risk reduction and absolute risk reduction as well as number needed to treat if available)
None reported
Outcome: Exploratory endpoints (Report both relative risk reduction and absolute risk reduction as well as number needed to treat if available)
None reported
Outcome: Safety endpoints (Report both relative risk and absolute risk as well as number needed to harm if available)
None reported
Conclusions of the Investigators (Quote the investigators conclusions here)
None reported
Commentary, Discussion and Limitations of the Trial (Anyone can add comments)
None reported
Slides
None reported
Video Commentary
None reported
References (How to insert a reference)
None reported
External sites for further information (How to insert links)
None reported
Detailed information about the trial
Ages
__ years to ___ years
Gender (Indicate whether men, women or both were enrolled)
None reported
Accepts Healthy Volunteers (Answer yes or no)
None reported
Enrollment Period (Study start and end date)
None reported
Recruitment Status (explanation)
None reported
Enrollment (Total number of patients enrolled)
None reported
Study Sponsor (e.g. Investigator initiated or company name)
None reported (this may not have yet been ascertained)
Source of Data (Where is this data on this page coming from: publication, principal investigator, or co-investigator)
None reported
The content of the clinical trial wiki consists of fields that have been suggested by the World Health Organization and wwww.clinicaltrials.gov.