Models:
Joseph Gordon
joseph-gordon/
ClinicalTrialsElig
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Downloads: 1
[c09aa8]: / clusters / final9knumclusters / clust_827.txt

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Subject or subject's representative is willing and able to provide written informed consent

Willing and able to give written informed consent.

Patient is able and willing to provide written informed consent

Be willing and able to provide written informed consent for the trial

Patient must be capable, willing, and able to provide written, informed consent

Willing and able to provide written informed consent.

Be willing and able to provide written informed consent for the trial

Willing and able to provide written informed consent

Be willing and able to provide written informed consent for the trial

Able and willing to provide written informed consent to participate in this study.

Willing and able to provide written informed consent for the study

Be willing and able to provide written informed consent for the trial

Be willing and able to provide written informed consent for the trial

Be willing and able to provide written informed consent for the trial

Willing and able to provide written informed consent for the trial

Be willing and able to provide written informed consent for the trial

Willing and able to give written, and dated, informed consent

Willing and able to provide written informed consent to participate in this investigational study.

Subject is willing and able to give prior written informed consent for investigation participation; and

Willing and able to give written informed consent

Willing and able to give written informed consent

Must be able and willing to give written informed consent.

Subjects must be willing to give written informed consent per institutional guidelines and must be able and willing to adhere to dose and visit schedules

Must be willing and able to provide written informed consent

Be willing and able to provide written informed consent for the trial

Willing and able to provide written informed consent

Be willing and able to provide written informed consent for the trial

Be willing and able to provide written informed consent for the trial.

Be willing and able to provide written informed consent.

Be willing and able to provide written informed consent for the trial

Willing and able to provide written informed consent for the trial

Be willing and able to provide written informed consent for the trial

Patient must be willing and able to provide written informed consent for the trial

Be willing and able to provide written informed consent for the trial

Be willing and able to provide written informed consent for the trial

Must be willing and able to provide written informed consent

Be willing and able to provide written informed consent for the trial

Willing to provide informed written consent

Be willing and able to provide written informed consent for the trial

Willing and able to provide written informed consent.

Be willing and able to provide written informed consent for the trial

Willing and able to provide written informed consent

Willing and able to provide written informed consent for the trial

Is willing and able to provide written informed consent for the trial.

Be willing and able to provide written informed consent for the trial

Be willing and able to provide written informed consent for the trial

Be willing and able to provide written informed consent for the trial

Willing and able to provide written informed consent

Be willing and able to provide written informed consent for the trial

Willing and able to provide written informed consent

Willing and able to provide written informed consent

Must be willing and able to provide written informed consent

Be willing and able to provide written informed consent for the trial

Subjects must be willing to give written informed consent per institutional guidelines and must be able and willing to adhere to dose and visit schedules

Willing and able to provide written informed consent

Be willing and able to provide written informed consent for the trial

Be willing and able to provide written informed consent for the trial

Willing and able to provide written informed consent

Be willing and able to provide written informed consent for the trial

Be willing and able to provide written informed consent for trial

Be willing and able to provide written informed consent for the trial

Be willing and able to provide written informed consent for the trial.

Be willing and able to provide written informed consent for the trial

Is willing and able to provide written informed consent for the trial

Must be able and willing to give written informed consent

Be willing and able to provide written informed consent for the trial

Patient must be capable, willing, and able to provide written, informed consent

Willing and able to give written informed consent

Must be willing and able to provide written informed consent

Willing and able to give written informed consent

Willing and able to provide written informed consent.

Be willing and able to provide written informed consent

Be willing and able to provide written informed consent for the trial

Be willing and able to provide written informed consent for the trial

Be willing and able to provide written informed consent for the trial.

Must be able and willing to give written informed consent

Willing and able to provide written informed consent for the trial

Be willing and able to provide written informed consent for the trial

Be willing and able to provide written informed consent for the trial

Willing and able to provide written informed consent for voluntary participation in the trial

Be willing and able to provide written informed consent for the trial

Be willing and able to provide written informed consent for the trial

Participant is willing and able to give written informed consent

Patient is willing and able to give written informed consent

Willing and able to provide written informed consent

Able and willing to provide written informed consent

Patient willing and able to provide written informed consent

Willing to provide written informed consent

Must be able and willing to give written informed consent

Able and willing to provide written informed consent to participate in the study

Patients must be able and willing to give written informed consent

Be willing and able to provide written informed consent

Be willing and able to provide written informed consent for the trial.

Be willing and able to provide written informed consent for the trial

Must be willing and able to provide written informed consent

Must be willing and able to provide written informed consent

Willing and able to give written informed consent.

Be willing and able to provide written informed consent for the trial

Willing and able to provide informed written consent

Able and willing to provide written informed consent

Be willing and able to provide written informed consent for the trial

Willing and able to give written informed consent

Patient must be capable, willing, and able to provide written, informed consent

Patient willing and able to provide written informed consent for the trial

Willing and able to provide written informed consent

Able and willing to provide written informed consent.

Willing and able to give written informed consent

Willing and able to give written informed consent

Willing and able to give written informed consent

Willing and able to provide written Informed Consent and adhere to study procedures.

Willing and able to provide written informed consent

Willing and able to give written informed consent

Willing and able to provide written informed consent.

Willing and able to provide written informed consent

Able and willing to give written informed consent.

4. Patient is able and willing to provide written informed consent to participate in the study.

Subject or subject's representative is willing and able to provide written informed consent

Subjects must be willing to give written informed consent and be able to adhere to dose and visit schedules.

Willing and able to provide written informed consent.

Willing and able to give written informed consent

Subject is willing to provide written informed consent

Able and willing to provide written consent

Willing to provide informed written consent

Willing and able to provide written informed consent

Patients must be willing and able to provide a written informed consent

Able and willing to provide written informed consent

Patients must be willing and able to provide written informed consent for the trial

Willing and able to provide written informed consent

Patient must be able and willing to provide written informed consent

Participant willing to provide a written informed consent

Willing and able to provide written informed consent

Subject must be able and willing to give written informed consent for a contrast enhanced ultrasound study of the prostate

Willing and able to provide informed written consent

Be willing and able to provide written informed consent for the trial

Willing and able to provide a written informed consent

Willing and able to provide written informed consent

Subjects are required to be willing and able to provide written informed consent

Be willing and able to provide written informed consent.

Patients must be able and willing to provide written informed consent prior to any study related procedure.

Be willing and able to provide written informed consent for the trial