Template to add a clinical trial: Difference between revisions

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<font color="blue">How to edit trial information:</font> <small> [[Special:UserLogin|Log in]], click on the word edit, type in the appropriate information, click save page at the bottom when you are done.</small>
<font color="blue">How to edit trial information:</font> <small> [[Special:UserLogin|Log in]], click on the word <nowiki>[<font color="blue">edit</font>]</nowiki> to the right of the section you would like to edit, type in the appropriate information, click save page at the bottom when you are done.</small>


== Complete Title of Study ==
== Complete Title of Study ==

Revision as of 12:57, 17 May 2009

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List of terms related to Template to add a clinical trial

How to edit trial information: Log in, click on the word [<font color="blue">edit</font>] to the right of the section you would like to edit, type in the appropriate information, click save page at the bottom when you are done.

Complete Title of Study

None reported

Study Acronym (The trial's abbreviation if there is one)

None reported

Overview of Template to add a clinical trial

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Disease State(s) Studied (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)

None reported

Study Arms and How They Were Treated (Intervention) (Explanation here)

None reported

Primary Pre-Specified Endpoint

None reported

Secondary Endpoints

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Inclusion Criteria

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Exclusion Criteria

None reported

Ages

__ years to ___ years

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

Gender (Indicate whether men, women or both were enrolled)

None reported

Study Sponsor (e.g. Investigator initiated or company name)

None reported

Source of Data (Who is providing this data: publication, principal investigator, or co-investigator)

None reported

Collaborators

None reported

Investigators

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Oversight Authority (e.g. FDA, EMEA)

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Medline PMIDs

None reported

External sites for further information (How to insert links)

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References (How to insert a reference)

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