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Vanderbilt University Institutional Review Board Informed Consent Document for Research Principal Investigator: T. Alp Killer, MD Revision Date: 06/02/2015 Study Title: Nutrition, Inflammation and

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How to fill out prs - clinicaltrialsgov final

01

Here is a step-by-step guide to fill out PRS on clinicaltrialsgov final:

02

Visit the clinicaltrialsgov website and login to your account.

03

Click on the 'Register and Submit Studies' tab.

04

Select the option 'Create a new study record' on the left side.

05

Fill in the required fields such as title, brief summary, and study design.

06

Provide detailed information about the study protocol, eligibility criteria, and interventions.

07

Upload all necessary documents and resources related to the study.

08

Review the filled information and make any necessary edits or corrections.

09

Submit the completed PRS form for review and approval.

10

Wait for the review process and any requested revisions.

11

Once approved, your study record will be published on clinicaltrialsgov.

Who needs prs - clinicaltrialsgov final?

01

Anyone who is conducting a clinical trial and wishes to register it on clinicaltrialsgov platform needs to fill out PRS - clinicaltrialsgov final.

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What is prs - clinicaltrialsgov final?

PRS - ClinicalTrials.gov final refers to the final submission of results information on ClinicalTrials.gov database.

Who is required to file prs - clinicaltrialsgov final?

The responsible party or sponsor of a clinical trial is required to file PRS - ClinicalTrials.gov final.

How to fill out prs - clinicaltrialsgov final?

To fill out PRS - ClinicalTrials.gov final, the responsible party needs to navigate to the website, log in to their account, and follow the prompts to submit the required information.

What is the purpose of prs - clinicaltrialsgov final?

The purpose of PRS - ClinicalTrials.gov final is to publicly disclose the results of a clinical trial to ensure transparency and accountability in research.

What information must be reported on prs - clinicaltrialsgov final?

Information such as the trial's primary and secondary outcomes, adverse events, participant demographics, and statistical analysis must be reported on PRS - ClinicalTrials.gov final.

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