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FOR WHO USE Validate received by WHO:Thematic area:Single site proposal “Core proposal (for multigenre study)Genre-specific proposal under multigenre studyConnect ID No:HIP Research ProposalTrial
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To fill out and find out about trials, follow these steps:
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Research: Start by conducting research to find trials that may be relevant to your needs. Use online resources such as clinical trial registries, medical journals, or websites like ClinicalTrials.gov. Additionally, consult with your healthcare provider for recommendations.
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Review eligibility criteria: Once you have identified a potential trial, carefully review the eligibility criteria provided by the trial investigators. This includes factors such as age, medical condition, previous treatments, and other specific requirements.
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Contact trial investigators: If you meet the eligibility criteria and are interested in participating, contact the trial investigators to express your interest and inquire about the enrollment process. They will provide you with necessary information and guide you through the next steps.
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Informed consent: Before participating in any clinical trial, you will need to provide informed consent. This involves thoroughly understanding the purpose, risks, and potential benefits of the trial. Take the time to read and comprehend all relevant documents, ask questions, and seek clarification if needed.
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Undergo screening: Once you have provided informed consent, the trial investigators will conduct a screening process to determine your suitability for the trial. This may involve various assessments, tests, and medical examinations.
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Participate in the trial: If you pass the screening process, you will begin participating in the trial according to the study protocol. This can include receiving study medications or interventions, attending regular follow-up visits, and adhering to any specific instructions or guidelines.
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Monitor and report: Throughout the trial, you will be closely monitored by the trial investigators to assess your response to the intervention and monitor any potential side effects or adverse events. It is important to communicate any changes or concerns to the trial team.
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Follow-up and results: After the trial is completed, there may be a follow-up period where you will continue to be monitored. The trial investigators will analyze the data collected and provide you with the results of the trial if applicable.
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Note: It is crucial to consult with your healthcare provider and consider the potential risks and benefits before participating in any clinical trial.

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Overall, anyone interested in advancing medical knowledge, exploring new treatment options, or contributing to scientific research may find it beneficial to find out about trials.

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