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Protocol No:Sponsor:22HH7931Imperial College London 6.0 18th December 2023CLINICAL STUDY PROTOCOL STUDY COORDINATION Center: Imperial College LondonFull Study Title:PROTECT HF: Physiological vs Right
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How to fill out a prospective case series

How to fill out a prospective case series
01
Define the research question or hypothesis that the case series will address.
02
Identify the target population that will be included in the case series.
03
Develop a data collection plan and determine the variables to be measured.
04
Obtain ethical approval for the study if necessary.
05
Recruit participants and obtain informed consent.
06
Collect data according to the predefined plan.
07
Analyze the data and report the findings.
Who needs a prospective case series?
01
Researchers conducting clinical studies to evaluate the safety and efficacy of a new treatment.
02
Public health officials investigating an outbreak of a particular disease.
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Healthcare providers looking to better understand a rare medical condition.
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Policy makers interested in assessing the impact of a public health intervention.
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What is a prospective case series?
A prospective case series is a type of observational study that follows a group of individuals who are receiving a specific treatment or intervention over time, collecting data on their outcomes and experiences.
Who is required to file a prospective case series?
Generally, researchers or healthcare professionals conducting studies involving new treatments or interventions are required to file a prospective case series.
How to fill out a prospective case series?
Filling out a prospective case series involves collecting data systematically on participant demographics, treatments administered, medical outcomes, and follow-up information.
What is the purpose of a prospective case series?
The purpose of a prospective case series is to evaluate the effectiveness and safety of a treatment or intervention in real-time with data collected from participants.
What information must be reported on a prospective case series?
Information that must be reported includes participant demographics, treatment details, outcomes observed, any adverse events, and follow-up results.
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