Objectives Randomised clinical trials (RCTs) are costly and published information on resource requirements for their conduct is limited. To identify key factors for making RCTs more sustainable, empirical data on resource use and associated costs are needed. We aimed to retrospectively assess resource use and detailed costs of two academic, investigator-initiated RCTs using a comprehensive list of cost items. Study Desgn and Setting The resource use of two investigator-initiated RCTs (Prednisone-Trial [NCT00973154] and Oxantel-Trial [ISRCTN54577342]) was empirically assessed in a standardized manner through semi-structured interviews and a systematically developed cost item list. Using information about yearly salaries, resource use was tra...
AbstractClinical trials evaluating medicines, medical devices, and procedures now commonly assess th...
The preparation of a randomized controlled trial (RCT) requires substantial resources and the admini...
Objectives: To perform value of information (VOI) analyses, an estimate of research costs is needed....
Objectives Randomised clinical trials (RCTs) are costly and published information on resource requir...
Objectives Randomised clinical trials (RCTs) are costly. We aimed to provide a systematic overview o...
Healthcare costs, particularly pharmaceutical costs, are a dominant issue for most healthcare organi...
OBJECTIVES We aimed to provide a systematic overview of freely available tools which may help plan ...
Background: Electronic health records (EHRs) may support randomized controlled trials (RCTs). We aim...
AbstractBackgroundThe UK Health Technology Assessment (HTA) program funds trials that address issues...
Electronic health records (EHRs) may support randomized controlled trials (RCTs). We aimed to descri...
BACKGROUND: The costs of medical research are a concern. Clinical Trials Units (CTUs) need to better...
Background The preparation of a randomized controlled trial (RCT) requires substantial resources and...
Background: A large fraction of the cost of conducting clinical trials is allocated to recruitment o...
AbstractClinical trials evaluating medicines, medical devices, and procedures now commonly assess th...
The preparation of a randomized controlled trial (RCT) requires substantial resources and the admini...
Objectives: To perform value of information (VOI) analyses, an estimate of research costs is needed....
Objectives Randomised clinical trials (RCTs) are costly and published information on resource requir...
Objectives Randomised clinical trials (RCTs) are costly. We aimed to provide a systematic overview o...
Healthcare costs, particularly pharmaceutical costs, are a dominant issue for most healthcare organi...
OBJECTIVES We aimed to provide a systematic overview of freely available tools which may help plan ...
Background: Electronic health records (EHRs) may support randomized controlled trials (RCTs). We aim...
AbstractBackgroundThe UK Health Technology Assessment (HTA) program funds trials that address issues...
Electronic health records (EHRs) may support randomized controlled trials (RCTs). We aimed to descri...
BACKGROUND: The costs of medical research are a concern. Clinical Trials Units (CTUs) need to better...
Background The preparation of a randomized controlled trial (RCT) requires substantial resources and...
Background: A large fraction of the cost of conducting clinical trials is allocated to recruitment o...
AbstractClinical trials evaluating medicines, medical devices, and procedures now commonly assess th...
The preparation of a randomized controlled trial (RCT) requires substantial resources and the admini...
Objectives: To perform value of information (VOI) analyses, an estimate of research costs is needed....