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Participation was based on signed informed consent.
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All human subjects were briefed on procedures and signed informed consent documentation.
All respondents signed informed consent on entering the study.
The ascites were obtained on Institutional Review Board approved protocols and patients signed informed consent.
Although gefitinib was supplied on a named-patient basis, all patients provided signed, informed consent.
All patients signed informed consent to allow molecular research on specimen obtained during surgical operation.
Data on demographic characteristics and drug abuse were collected from individuals who signed informed consent forms.
Sixteen healthy males provided signed informed consent prior to participation in this study, which was granted approval by the Coventry University Ethics committee, and were divided into 2 matched groups based on their aerobic capacity.
Participants signed informed consent.
All patients signed informed consent.
Participants gave signed informed consent.
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