--- a
+++ b/clusters/9knumclustersv2/clust_1387.txt
@@ -0,0 +1,55 @@
+Ability to provide signed Informed Consent Form
+Be  years of age at the time the informed consent form is signed
+Provide written informed consent prior to any study related procedure. (In the event that the patient is re-screened for study participation or a protocol amendment alters the care of an ongoing patient, a new informed consent form must be signed.)
+Be  years old at the time the informed consent form is signed
+Signed informed consent form
+Patient or authorized proxy needs to have signed the informed consent form
+Signed Informed consent form
+Signed Informed Consent Form.
+Subject has been informed of the study procedures and the treatment and has signed an informed consent form
+Signed informed consent form in accordance with institutional policies prior to the initiation of high-dose therapy
+Signed informed consent form must be obtained prior to any research procedure
+Have signed the current approved informed consent form
+Signed written informed consent form
+Informed consent form signed by the subject
+Signed informed consent form must be obtained prior to any study procedure
+Signed Informed Consent Form
+Signed informed consent form
+Signed informed consent form
+Signed informed consent form
+Subjects provide signed written informed consent, which includes compliance with the requirements and restrictions listed in the consent form.
+Signed informed consent form.
+Patients must provide a signed informed consent form before any trial relates activities are carried out.
+A signed informed consent form or minor assent form
+A signed informed consent form or minor assent form
+Signed informed consent form
+Patient has provided a signed study informed consent form prior to performance of any study related procedure
+The signed informed consent form prior to the performance of any study related procedures that are not considered part of standard of care
+Signed informed consent form
+Signed informed consent form
+Patients who have not provided a signed informed consent form to participate in the study, obtained prior to the start of any protocol related activities.
+Patients must give written informed consent; a copy of the signed informed consent form will be retained in the patients chart
+Have signed an approved informed consent form for the study.
+Signed Informed Consent Form
+Signed Informed Consent Form
+Signed Informed Consent Form
+Signed Informed Consent Form
+Patients must have a signed informed consent form prior to enrollment on study
+Signed Informed Consent Form
+Signed Informed Consent Form
+Signed Informed Consent Form
+Signed Informed Consent Form
+The signed informed consent form
+Signed informed consent form
+(Patient participation) Signed written informed consent form
+Signed informed consent form
+Signed informed consent form from patient
+Provide signed written informed consent, which includes compliance with the requirements and restrictions listed in the consent form.
+Signed informed consent form
+Subjects must have signed an approved consent form
+Received and signed an informed consent form.
+Signed informed consent form
+Signed informed consent form.
+Subjects must have received and signed an informed consent form.
+Subjects must have received and signed an informed consent form.
+Signed Informed Consent Form