A surveillance system for monitoring, public reporting, and improving minority access to cancer clinical trials

Clinical Trials

Volumn 9, Issue 4, 2012, Pages 426-435

  Carpenter, William R ^a,b   Tyree, Seth ^b   Wu, Yang ^b   Meyer, Anne Marie ^b   Dimartino, Lisa ^b   Zullig, Leah ^a   Godley, Paul A ^b,c  

^a IL   (United States)

^b UNIVERSITY OF NORTH CAROLINA   (United States)

^c UNIVERSITY OF NORTH CAROLINA SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AGED; ARTICLE; CANCER REGISTRY; CANCER RESEARCH; CANCER THERAPY; CLINICAL TRIAL (TOPIC); FEMALE; GENDER; HEALTH CARE ACCESS; HUMAN; INCIDENCE; INFORMATION RETRIEVAL; INFORMATION SYSTEM; MAJOR CLINICAL STUDY; MALE; MANDATORY REPORTING; MINORITY GROUP; PATIENT SELECTION; PRIORITY JOURNAL; RACE; UNITED STATES;

ADULT; AGED; AGED, 80 AND OVER; FEMALE; HEALTH SERVICES ACCESSIBILITY; HEALTHCARE DISPARITIES; HUMANS; MALE; MIDDLE AGED; MINORITY GROUPS; MULTIVARIATE ANALYSIS; NEOPLASMS; NORTH CAROLINA; PATIENT SELECTION; POPULATION SURVEILLANCE; RANDOMIZED CONTROLLED TRIALS AS TOPIC; REGISTRIES;

EID: 84865463464     PISSN: 17407745     EISSN: 17407753     Source Type: Journal    
DOI: 10.1177/1740774512449531     Document Type: Article

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