Twelve institutional data managers were asked to independently code the data from a patient chart of one patient in an ovarian cancer trial. They abstracted data from the medical record and filled out three types of trial forms (on-study, chemotherapy, and summary forms). The analysis of the processed data revealed that the median rate of errors was 13% for the 12 data managers. The error rate differed among the types of trial forms. The factors causing these errors were mistakes in interpretation, documentation, and coding. The level of experience of the data managers proved to be an important factor. It became clear that the documentation in the medical record was inadequate. We conclude that data managers as well as physicians involved i...
Purpose: Medication errors (MEs) have been a significant problem resulting in excessive patient morb...
With the exponential expansion of clinical trials conducted in (Brazil, Russia, India, and China) an...
Attempting to collect too much data can result in lack of participation by patients and institutions...
Twelve institutional data managers were asked to independently code the data from a patient chart of...
BACKGROUND: Historically, only partial assessments of data quality have been performed in clinical t...
Background Clinical trials are an important research method for improving medical knowledge and pati...
Historically, only partial assessments of data quality have been performed in clinical trials, for w...
Background Substantial staff time and costs are incurred in the collection of data for cancer clinic...
For a clinical trial to be successful, it is necessary to possess high quality data fro...
Background: Although cancer treatment information has been collected through the Cancer Registry sys...
Methodological issues may limit the impact and application of patient-reported outcome (PRO) evidenc...
Background: A clinical data management system is a software supporting the data management process i...
Objectives: To assess quality and reusability of coded cancer diagnoses in routine primary care data...
Objectives: To assess quality and reusability of coded cancer diagnoses in routine primary care data...
Clinical Data Management (CDM) could be a crucial innovative clinical analysis, that ends up in the ...
Purpose: Medication errors (MEs) have been a significant problem resulting in excessive patient morb...
With the exponential expansion of clinical trials conducted in (Brazil, Russia, India, and China) an...
Attempting to collect too much data can result in lack of participation by patients and institutions...
Twelve institutional data managers were asked to independently code the data from a patient chart of...
BACKGROUND: Historically, only partial assessments of data quality have been performed in clinical t...
Background Clinical trials are an important research method for improving medical knowledge and pati...
Historically, only partial assessments of data quality have been performed in clinical trials, for w...
Background Substantial staff time and costs are incurred in the collection of data for cancer clinic...
For a clinical trial to be successful, it is necessary to possess high quality data fro...
Background: Although cancer treatment information has been collected through the Cancer Registry sys...
Methodological issues may limit the impact and application of patient-reported outcome (PRO) evidenc...
Background: A clinical data management system is a software supporting the data management process i...
Objectives: To assess quality and reusability of coded cancer diagnoses in routine primary care data...
Objectives: To assess quality and reusability of coded cancer diagnoses in routine primary care data...
Clinical Data Management (CDM) could be a crucial innovative clinical analysis, that ends up in the ...
Purpose: Medication errors (MEs) have been a significant problem resulting in excessive patient morb...
With the exponential expansion of clinical trials conducted in (Brazil, Russia, India, and China) an...
Attempting to collect too much data can result in lack of participation by patients and institutions...