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Get the free END OF TRIAL PARTICIPATION FORM PR08 Form 20 Page 11

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PR08 STAMPEDE END OF TRIAL PARTICIPATION FORM PR08 Form 20-Page 1/1 Please return to: STAMPEDE trial, MRC Clinical Trials Unit, Aviation House, 125 King sway, London, WC2B 6NH Patient initials: Hospital:.
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How to fill out end of trial participation:

01
Obtain the end of trial participation form from the organization conducting the trial.
02
Read the instructions provided on the form carefully to understand the requirements and any specific information you need to provide.
03
Fill in your personal details accurately, including your full name, contact information, and any identification numbers or trial participant IDs given to you during the trial.
04
Provide information about the trial you participated in, such as the trial name, location, dates of participation, and any specific details requested on the form.
05
Summarize your experience during the trial, mentioning any positive or negative observations, side effects, or significant changes you noticed in your health.
06
If required, provide any additional information or documentation requested, such as medication logs, diaries, or any other records kept during the trial.
07
Sign and date the form, ensuring that all the required fields have been filled out accurately.
08
Return the completed form to the designated organization or individual as instructed, following any specific submission guidelines mentioned on the form or provided separately.

Who needs end of trial participation?

01
Participants of clinical trials or research studies who have reached the end of the designated trial period.
02
Individuals who have completed their assigned trial interventions or treatments and are required to provide feedback or data on their trial experience.
03
Researchers, organizations, or regulatory authorities conducting the trial who need comprehensive information and feedback from trial participants to analyze the efficacy, safety, or outcomes of the trial.
Remember, it is important to follow any specific instructions or guidelines provided by the trial organization or research team when filling out the end of trial participation form to ensure accurate and useful information is provided.
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End of trial participation refers to the completion of a clinical trial by study participants.
The principal investigator or sponsor of the clinical trial is typically required to file end of trial participation.
End of trial participation is usually filled out by documenting the final outcomes of the clinical trial and any relevant data.
The purpose of end of trial participation is to provide a summary of the clinical trial results and conclusions.
End of trial participation must include details on the study participants, trial outcomes, and any adverse events.
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