Dying children and medical research: Access to clinical trials as benefit and burden

American Journal of Law and Medicine

Volumn 29, Issue 2-3, 2003, Pages 301-317

  Oberman, Michelle ^a,b   Frader, Joel ^b,c,d  

^a DEPAUL UNIVERSITY   (United States)

^b CHILDREN'S MEMORIAL HOSPITAL   (United States)

^c NORTHWESTERN UNIVERSITY   (United States)

^d Gen Acad and Emergency Pediatrics   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BODY BURDEN; CHILD ABUSE; CLINICAL RESEARCH; CLINICAL TRIAL; CONFERENCE PAPER; CUSTODY; DYING; GRIEF; HEALTH CARE ACCESS; HUMAN EXPERIMENT; INFORMED CONSENT; LEGAL ASPECT; MEDICAL ETHICS; MEDICAL RESEARCH; RISK BENEFIT ANALYSIS; TERMINAL DISEASE; ARTICLE; BIOMEDICAL AND BEHAVIORAL RESEARCH; CHILD; CHILD WELFARE; CONFLICT OF INTEREST; HISTORY; HUMAN; HUMAN RELATION; METHODOLOGY; NEOPLASM; PATIENT SELECTION; PHASE 1 CLINICAL TRIAL; PHYSICIAN; RISK ASSESSMENT; TERMINAL CARE;

BIOMEDICAL AND BEHAVIORAL RESEARCH;

BIOMEDICAL RESEARCH; CHILD; CHILD WELFARE; CLINICAL TRIALS, PHASE I; CONFLICT OF INTEREST; ETHICS, MEDICAL; HISTORY, 20TH CENTURY; HUMANS; NEOPLASMS; PATIENT SELECTION; PHYSICIANS; RESEARCHER-SUBJECT RELATIONS; RISK ASSESSMENT; TERMINAL CARE; THERAPEUTIC HUMAN EXPERIMENTATION;

EID: 0642310428     PISSN: 00988588     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Conference Paper

References (0)