<http://webisa.webdatacommons.org/356678261>	<http://www.w3.org/ns/prov#value>	"Feasibility studies to test and optimize parameters such as accrual rates, acceptance of randomization, compliance, delivery of the intervention, appropriate inclusion/exclusion criteria, and optimization of the overall protocol design for planned clinical trials." .
<http://webisa.webdatacommons.org/356678261>	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/ns/prov#Entity> .
<http://webisa.webdatacommons.org/prov/193100201>	<http://www.w3.org/ns/prov#wasDerivedFrom>	<http://webisa.webdatacommons.org/356678261> .
<http://webisa.webdatacommons.org/356678261>	<http://www.w3.org/ns/prov#wasQuotedFrom>	<nih.gov> .