… Guidelines on informed consent intend to protect patients and promote ethical research …
In an analysis of 107 consent forms from cancer clinical trials, none was written at or below 8th …

… lung cancer (N = 22) were randomly assigned to receive either an original consent document
or … were conducted after the patients had read the consent documents. The interviews were …

… patient comprehension [22–26]. Such inadequacies stem from a failure to develop consent
documents that correspond to patient … that a detailed document containing comprehensive …

… The present study indicdtes that the degree to which the informed consent document is
understood and subject to recall varies according to sex and may vary according to age. Men in …

… IRB and the Clinical Research Review Committee of the Winship Cancer Institute. The …
First, although the intended purpose of the consent document is to aid the patient in making a …

… The variations in national laws, regulations, and cultures contribute to complex informed
consent documents for patients participating in clinical trials. Currently, only few ethics …

… consent for clinical research includes 2 components: informed consent documents (ICDs)
and informed consent … Of the 69 patients included in the current study, 42 (61%) were male, …

… All clinical trials on cancer patients approved by the REC in the central region of Norway …
II and III studies testing drugs in cancer patients (eg medical treatment of cancer pain, cytotoxic …

… In our experience, sponsoring companies approach informed-consent documents as
compulsory legal regulatory requirements. We believe that clinical researchers and the Ethics' …

… of informed consent for pediatric cancer trials. Furthermore, most studies have examined …
, physicians, and patient (when appropriate) shortly after the patient's diagnosis with either …