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CANADIANAUSTRALASIAN Randomized TRIAL SCREENING KIDNEY TRANSPLANT CANDIDATES CORONARY ARTERY DISEASE(CARS STUDY)Protocol Number: 1Version: 6Date: 22/03/2018Author/s:Steve Chadian, Angela Webster,
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To fill out a Canadian-Australasian Randomised Trial (CART) document, follow these steps:
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Start by reading the instructions and guidelines provided with the document.
03
Fill in the basic information, such as the title of the trial, investigator's name, and contact details.
04
Provide a brief background and rationale for the trial.
05
Describe the study design, including randomization and blinding procedures.
06
Outline the intervention or treatment being tested and the control group.
07
Specify the eligibility criteria for participants, including age, gender, and any relevant medical conditions.
08
Detail the study procedures, such as data collection methods, follow-up assessments, and any expected adverse events.
09
Include information about the sample size calculation and statistical analysis plan.
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Describe any ethical considerations and obtain necessary approvals.
11
Provide a timeline for the trial, including the recruitment period and expected duration.
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Include a section for potential conflicts of interest and funding sources.
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Review the completed document for any missing or inconsistent information.
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Submit the filled out CART document to the appropriate regulatory authorities or ethics committees.

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The Canadian-Australasian Randomised Trial (CART) document is needed by researchers, clinicians, and organizations conducting clinical trials that fall within the scope of CART. It is also required by regulatory authorities and ethics committees to ensure that the trial is conducted in a rigorous and ethical manner. Additionally, participants in the trial may also benefit from understanding the trial details provided in the CART document.
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The Canadian-Australasian Randomised Trial document is a form used to record information and data from a research study that is conducted in Canada and Australasia.
The researchers and investigators conducting the study are required to file the Canadian-Australasian Randomised Trial document.
The document is typically filled out by entering the required information and data in the designated fields provided in the form.
The purpose of the Canadian-Australasian Randomised Trial document is to record and report important information and data from a research study for review and analysis.
The document typically requires information such as study objectives, methodology, results, conclusions, and any relevant findings.
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