How to add a trial to the clinical trials wiki: Difference between revisions
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== Complete Title of Study == | == 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 <small>(The trial's abbreviation if there is one) </small>== | ==Study Acronym <small>(The trial's abbreviation if there is one) </small>== | ||
Often a trial will have an abbreviation, and this is called an acronym. Place that here. Also make sure that the acronym redirect to this page. To learn how to redirect a page click here | |||
==Principal Investigator, Co-investigators, and Collaborating Institutions== | ==Principal Investigator, Co-investigators, and Collaborating Institutions== |
Revision as of 12:36, 18 May 2009
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.
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 redirect to this page. To learn how to redirect a page click here
Principal Investigator, Co-investigators, and Collaborating Institutions
None reported
Overview of Trial
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Disease State(s) Studied (e.g. acute MI, breast cancer, etc.)
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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)
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Study Arms and How They Were Treated (Intervention) (Explanation here)
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Primary Pre-Specified Endpoint
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Secondary Endpoints
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Inclusion Criteria
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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)
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Commentary, Discussion and Limitations of the Trial (Anyone can add comments)
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Slides
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Video Commentary
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References (How to insert a reference)
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External sites for further information (How to insert links)
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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.