Template to add a clinical trial: Difference between revisions

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<small>Click on the word edit and 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 [<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. The template is the minimum elements required by the World Health Organization. You can add additional sections.</small> [[Help:How to add a trial to the clinical trial wiki|More help to add a trial here.]]
 


== Complete Title of Study ==
== Complete Title of Study ==
None reported
None reported


==Study Acronym==
==Study Acronym <small>(The trial's abbreviation if there is one) </small>==
None reported
 
==Principal Investigator, Co-investigators, and Collaborating Institutions==
None reported
None reported


==Overview of {{PAGENAME}}==
==Overview of Trial==
None reported
None reported


==Study Design==
==Disease State(s) Studied <small>(e.g. acute MI, breast cancer, etc.)</small>==
None reported
None reported


== Primary Pre-Specified Endpoint ==
==Study Phase <small>(e.g. Phase I,II,III,IV) [[Study phase|Study Phases are defined here]]</small>==
None reported
 
==Study Design <small>(e.g. multicenter, randomized, double blind, placebo controlled)</small>==
None reported
 
== Study Arms and How They Were Treated (Intervention) <small>[[Study arms|(Explanation here)]]</small>==
None reported
None reported


== Secondary Outcomes ==
== Primary Pre-Specified Endpoint ==
None reported
None reported


== Interventions ==
== Secondary Endpoints ==
None reported
None reported


Line 30: Line 40:
None reported
None reported


== Study Arms ==
==Outcome: Primary endpoint <small>(Report both relative risk reduction and absolute risk reduction as well as number needed to treat if available)</small>==
None reported
 
==Outcome: Secondary endpoint <small>(Report both relative risk reduction and absolute risk reduction as well as number needed to treat if available)</small>==
None reported
None reported


==Disease State(s) Studied==
==Outcome: Exploratory endpoints <small>(Report both relative risk reduction and absolute risk reduction as well as number needed to treat if available)</small>==
None reported
None reported


==Intervention(s)==
==Outcome: Safety endpoints <small>(Report both relative risk and absolute risk as well as number needed to harm if available)</small>==
None reported
None reported


==Study Phase==
==Conclusions of the Investigators <small>(Quote the investigators conclusions here)</small>==
None reported
None reported


==Study Design==
==Commentary, Discussion and Limitations of the Trial<small> (Anyone can add comments)</small>==
None reported
None reported


==Enrollment Period==
==Slides==
None reported
None reported


==Recruitment Status [[Recruitment status|(explanation)]]==
==Video Commentary==
None reported
None reported


==Enrollment==
== References [[Help:Adding_References_to_Articles|(How to insert a reference)]]==
None reported
None reported


==Gender <small>(Indicate whether men, women or both were enrolled)</small>==
==External sites for further information <small>[[Help:Links|(How to insert links)]]</small>==
None reported
None reported


==Detailed information about the trial==
==Ages==
==Ages==
__ years to ___ years  
__ years to ___ years  
==Gender <small>(Indicate whether men, women or both were enrolled)</small>==
None reported


==Accepts Healthy Volunteers <small>(Answer yes or no)</small>==
==Accepts Healthy Volunteers <small>(Answer yes or no)</small>==
None reported
None reported


==Study Sponsor <small>(e.g. Investigator initiated or company name)</small>==
==Enrollment Period <small>(Study start and end date)</small>==
None reported
None reported


==Source of Data==
==Recruitment Status [[Recruitment status|(explanation)]]==
None reported
None reported


==Collaborators==
==Enrollment <small>(Total number of patients enrolled)</small>==
None reported
None reported


==Investigators==
==Study Sponsor <small>(e.g. Investigator initiated or company name)</small>==
None reported
None reported (this may not have yet been ascertained)


==Oversight Authority <small>(e.g. FDA, EMEA)</small>==
==Source of Data <small>(Where is this data on this page coming from: publication, principal investigator, or co-investigator)</small>==
None reported
None reported


==Medline PMIDs==
None reported


==External sites for further information [[Help:Links|(How to insert links)]]==
The content of the clinical trial wiki consists of fields that have been suggested by the World Health Organization and wwww.clinicaltrials.gov.
None reported


== References [[Help:Adding_References_to_Articles|(How to insert a reference)]]==
[[Category:Clinical trials]]
None reported


{{WH}}
{{WH}}


{{WS}}
{{WS}}

Latest revision as of 13:25, 4 June 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 [edit] 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. The template is the minimum elements required by the World Health Organization. You can add additional sections. More help to add a trial here.


Complete Title of Study

None reported

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

None reported

Principal Investigator, Co-investigators, and Collaborating Institutions

None reported

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.

Template:WH

Template:WS