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University of PennsylvaniaInformed Consent Form NCT02744352Madaan, Animal 8242017UNIVERSITY OF PENNSYLVANIA RESEARCH SUBJECT INFORMED CONSENT AND HIPAA AUTHORIZATION FORM Protocol Title: Comparison
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01
Start by reading the informed consent form thoroughly.
02
Make sure you understand the purpose of the study, the procedures involved, and any potential risks or benefits.
03
Fill in your personal information accurately, including your name, age, gender, and contact details.
04
Answer the questions about your medical history honestly and provide any relevant information.
05
If you have any questions or concerns, don't hesitate to ask the research team for clarification.
06
Sign and date the form to indicate your informed consent to participate in the study.
07
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Who needs informed consent form nct02744352?

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Anyone who wishes to participate in the clinical trial with the identification number nct02744352 needs to fill out an informed consent form. This ensures that participants understand the study's purpose, procedures, and potential risks, and have provided their voluntary consent to participate.
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The informed consent form for NCT02744352 is a document designed to provide potential participants with the necessary information about a clinical trial, including its purpose, procedures, risks, and benefits, ensuring they can make an informed decision about their participation.
The primary investigator or the research team conducting the clinical trial is required to file the informed consent form NCT02744352 to ensure ethical standards and compliance with regulatory requirements.
To fill out the informed consent form NCT02744352, participants must read the document carefully, ask any questions they may have, and sign it to indicate their understanding and agreement to participate in the trial.
The purpose of the informed consent form NCT02744352 is to protect the rights and welfare of participants by ensuring they are fully informed about the clinical trial and can voluntarily choose to participate.
The informed consent form NCT02744352 must include information such as the study's purpose, duration, procedures, risks and benefits, alternative treatments, and contact information for questions.
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Relevant keywords

2017 2018 pennsylvania uphs xxxxxx v1 irb drf emr penn pacu fda nabil elkassabany msce clinicaltrials redisclose randomization ppmc operatively preregional nct02744352 pennsylvanias researchrelated hipaa madaan anmol infraclavicular randomized analgesia d

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