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INFORMED CONSENT TO PARTICIPATE IN A CLINICAL TRIAL Title of the study: Prospective randomized multi center study between two anesthetic techniques for implant placement in the posterior mandible.
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Participants who are considering or planning to participate in a clinical trial need to fill out the clinicaltrialsgovprovideddocs90informed consent form.
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The clinicaltrialsgovprovideddocs90informed consent form is a document that outlines the information provided to participants in a clinical trial, including the risks and benefits of participating.
Investigators conducting clinical trials are required to file the clinicaltrialsgovprovideddocs90informed consent form.
The clinicaltrialsgovprovideddocs90informed consent form should be filled out by providing all relevant information to participants in a clear and understandable manner.
The purpose of the clinicaltrialsgovprovideddocs90informed consent form is to ensure that participants are fully informed about the risks and benefits of participating in a clinical trial.
The clinicaltrialsgovprovideddocs90informed consent form must include information about the trial procedures, risks, benefits, and alternatives.
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