--- a
+++ b/clusters/9knumclustersv2/clust_1220.txt
@@ -0,0 +1,29 @@
+Patient or parent/guardian capable of providing informed consent
+Patient or parent/guardian capable of providing informed consent
+Willing to and capable of providing written informed consent prior to any study related procedures
+Patients must be capable of understanding and providing a written informed consent
+Must be capable of providing informed consent
+Caregiver capable of providing post-HCT care
+Patient understands the procedures and agrees to comply with the study requirements by providing written informed consent
+Adult donors must be an HLA -/ match with the patient and must be capable of providing informed consent
+Capable of providing informed consent and complying with trial procedures.
+Capable of providing informed consent
+Capability of providing informed consent
+Capable of providing informed consent and complying with trial procedures.
+Patient understands the procedures and agrees to comply with the study requirements by providing written informed consent
+DONOR: Adult donors must be must be a HLA -/ related haploidentical match with the patient and must be capable of providing informed consent
+Patient or parent/guardian capable of providing informed consent
+Patients capable of providing written, informed consent
+Patient (or legal representative where appropriate) must be capable of providing written informed consent.
+Capable of providing informed consent and complying with trial procedures.
+Capable of providing informed consent and complying with trial procedures.
+Patients must be capable of providing informed consent and must be willing to provide written informed consent prior to the start of any study-specific procedures.
+Capable of providing informed consent
+Providing informed consent
+DCG: Is capable of providing informed consent
+Providing informed consent
+Capable of providing informed consent
+Participants must be capable of providing written informed consent for study participation
+Willing to and capable of providing written informed consent prior to any study related procedures
+Be capable of providing informed consent and demonstrate a willingness to comply with all the study procedures and visits
+The patient must be considered legally capable of providing his or her own consent for participation in this study