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Comprehensive Cancer Center CCFU 62418Section of Hematology and OncologyPHASE II PILOT STUDY OF SUBSEQUENT LINE AND NIVOLUMAB FOR ADVANCED SMALL CELL LUNG CANCER Informed Consent Form to Participate
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01
To fill out the clinicaltrialsgov 74 nct03594474 informed consent, follow these steps:
02
Read the informed consent form thoroughly to understand all the information provided.
03
Make sure you comprehend the purpose of the clinical trial and the potential risks involved.
04
If you have any questions or concerns, consult with the principal investigator or the study coordinator.
05
Take enough time to consider all the information provided before making a decision.
06
If you agree to participate, sign the informed consent form.
07
Keep a copy of the informed consent form for your records.
08
Be aware that you have the right to withdraw your consent at any time during the trial.
09
Follow any additional instructions provided by the research team throughout the study.

Who needs clinicaltrialsgov 74 nct03594474informed consent?

01
Anyone who is considering participating in the clinical trial with the identification number 74 nct03594474 needs to fill out the clinicaltrialsgov 74 nct03594474 informed consent form.
02
This includes potential participants who are eligible based on the inclusion criteria set by the research protocol.
03
The informed consent form ensures that participants are fully informed about the trial, its objectives, risks, and their rights.
04
By completing the informed consent form, individuals demonstrate their willingness to be part of the study and provide their consent for data collection and analysis.
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The informed consent for clinical trial NCT03594474 is a document that outlines the details of the study, risks involved, and rights of the participants.
The researchers conducting the clinical trial are required to file the informed consent on clinicaltrials.gov for study NCT03594474.
The informed consent form can be filled out by including all relevant information about the study and obtaining signatures from the participants.
The purpose of the informed consent is to ensure that participants are aware of the study details, risks, and their rights before agreeing to participate.
The informed consent should include details of the study protocol, potential risks and benefits, confidentiality measures, and contact information for questions.
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