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Joseph Gordon
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ClinicalTrialsElig
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[c09aa8]: / clusters / final9knumclusters / clust_1349.txt

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Provide informed written consent

Provide written informed consent

Provide informed written consent

Provide written informed consent

Subjects must provide written informed consent to participate

Must provide written informed consent.

Provide written informed consent

Provide written informed consent

Willingness to provide informed written consent

Patients who can provide informed consent

Patients must provide written consent

Participant must voluntarily agree to provide written informed consent

Provide written informed consent

Provide informed written consent

Provide informed consent

Provide informed written consent

Provide informed written consent

Provide informed written consent

Provide informed written consent

Provide informed written consent

Provide informed written consent

Patients must provide written informed consent.

Provide written informed consent for the follow up protocol.

Refusal to provide written informed consent

Patients must provide informed consent

Provide written informed consent

Provide written informed consent

Provide written informed consent

Provide written informed consent

Provide informed written consent

Provide written informed consent

Provide informed written consent

Provide written informed consent

Provide informed written consent

Provide informed written consent

Provide written informed consent

Provide written informed consent

Provide informed written consent

Provide informed written consent

Provide informed written consent

Provide written informed consent

Patients must provide written informed consent

Provide written informed consent

Patients must provide written informed consent.

The patient must provide informed consent.

Provide informed written consent

Provide informed written consent

Patients must provide informed written consent

Patients must provide written informed consent

Provide informed written consent

Patients must provide informed written consent

Patients must provide written informed consent

Provide informed written consent

Patients must provide written informed consent

Provide written informed consent for the trial

Provide informed written consent

Must provide written informed consent

Participant must provide informed consent

Patients must provide written informed consent

Provide informed written consent

For Phase I and II: Patients must provide written informed consent.

Subjects who provide written informed consent to participate in the study

Willingness to provide written informed consent for the study.

Provide written informed consent prior to any study related procedure.

Provide informed written consent

Provide written informed consent to participate on the study

Patients must provide written consent

Provide written informed consent

Provide written informed consent

Provide written informed consent

Participant unwilling to provide written informed consent

Patients must provide written informed consent.

Provide written informed consent

Can provide informed consent

Provide written informed consent

Provide written informed consent

Provide informed written consent

Provide informed written consent

Provide informed written consent

Patients must provide informed written consent

Provide written informed consent

Provide informed written consent

Willingness to provide informed consent

Provide written informed consent

Provide written informed consent

Patients must provide verbal and written informed consent to participate in the study

Patients must provide written informed consent.

Willingness to provide written informed consent for the study.

Provide informed written consent

Participant must voluntarily agree to provide written informed consent.

Patients must provide written informed consent

Patients must provide written informed consent

Provide written informed consent

Provide written informed consent

Provide informed written consent

Provide informed written consent

Provide written informed consent

Provide informed written consent

Provide informed written consent

Provide informed written consent

Provide informed written consent

Provide informed written consent

Patients must provide informed consent

Patients must provide verbal and written informed consent to participate in the study

Patients must provide written informed consent prior to any registration on study

Provide informed written consent

Provide written informed consent

Provide informed written consent

Provide written informed consent (Screen 1 and Screen 2)

Provide informed written consent

Provide informed written consent

Patients must provide informed written consent

Provide informed written consent

Patients who provide written informed consent for participation in this trial

Provide informed written consent

Provide written informed consent

Provide informed consent

Provide written informed consent

Patients must provide written informed consent

Provide informed written consent

Patients must provide informed consent

Provide informed written consent

Willingness to provide written informed consent for the study.

Provide written informed consent.

Provide informed written consent

Patients must provide written informed consent.

Provide informed written consent

Provide written informed consent

Provide informed written consent

Provide informed written consent

Provide informed written consent

Provide written informed consent

Provide informed written consent

Patients must provide written informed consent

Provide informed written consent

Provide informed written consent

Provide written informed consent

Provide informed written consent

Both must provide informed consent

Provide written informed consent

Must provide written informed consent

Provide written informed consent

Provide written informed consent

Provide written informed consent prior to screening

Can provide informed consent

Provide informed written consent

Provide informed written consent

Provide informed written consent

Patients must provide written informed consent to participate in the study

Provide informed written consent

Provide informed consent

Patients can provide informed consent

Willingness to provide written informed consent

Provide written informed consent.

Provide written informed consent for the study

Cannot provide written informed consent

Cannot provide written informed consent

Provide informed written consent if >= 18 years; if < 18 years, provide informed written assent and parent or legal guardian provide informed written consent

Provide written informed consent

Patients must provide written informed consent

Cannot provide written informed consent

Provide informed written consent

Patients must provide informed written consent

Patients must provide written informed consent

Cannot provide written informed consent

Provide informed written consent

Can provide informed consent

Participants must voluntarily agree to provide written informed consent.