It is essential for the integrity of double-blind clinical trials that during the study course the individual treatment allocations of the patients as well as the treatment effect remain unknown to any involved person. Recently, methods have been proposed for which it was claimed that they would allow reliable estimation of the treatment effect based on blinded data by using information about the block length of the randomization procedure. If this would hold true, it would be difficult to preserve blindness without taking further measures. The suggested procedures apply to continuous data. We investigate the properties of these methods thoroughly by repeated simulations per scenario. Furthermore, a method for blinded treatment effect estim...
Blinding is a methodologic safeguard of treatment evaluation, yet severely understudied empirically....
Objectives: To explore the theoretical justification for blinding in randomized trials and make reco...
Aims During phase I study conduct, blinded data are reviewed to predict the safety of increasing the...
Regulatory authorities require that the sample size of a confirmatory trial is calculated prior to t...
When planning a randomized clinical trial, careful consideration must be given to how participants a...
It is well known that the outcome of an intervention is affected both by the inherent effects of the...
AbstractBlinding is a methodologic safeguard of treatment evaluation, yet severely understudied empi...
The determination of the appropriate sample size is an important aspect of planning a clinical trial...
The interaction between the patient\u27s expected outcome of an intervention and the inherent effect...
In combination with randomization, blinding or masking is an important factor in randomized controll...
It is well known that the outcome of an intervention is affected both by the inherent effects of the...
It is well known that the outcome of an intervention is affected both by the inherent effects of the...
BackgroundBlinding is the process of keeping treatment assignment hidden and is used to minimise the...
A key feature to many randomized, controlled trials is that they implement a blind; that is, subject...
In the planning phase of clinical trials there is often considerable uncertainty regarding the size ...
Blinding is a methodologic safeguard of treatment evaluation, yet severely understudied empirically....
Objectives: To explore the theoretical justification for blinding in randomized trials and make reco...
Aims During phase I study conduct, blinded data are reviewed to predict the safety of increasing the...
Regulatory authorities require that the sample size of a confirmatory trial is calculated prior to t...
When planning a randomized clinical trial, careful consideration must be given to how participants a...
It is well known that the outcome of an intervention is affected both by the inherent effects of the...
AbstractBlinding is a methodologic safeguard of treatment evaluation, yet severely understudied empi...
The determination of the appropriate sample size is an important aspect of planning a clinical trial...
The interaction between the patient\u27s expected outcome of an intervention and the inherent effect...
In combination with randomization, blinding or masking is an important factor in randomized controll...
It is well known that the outcome of an intervention is affected both by the inherent effects of the...
It is well known that the outcome of an intervention is affected both by the inherent effects of the...
BackgroundBlinding is the process of keeping treatment assignment hidden and is used to minimise the...
A key feature to many randomized, controlled trials is that they implement a blind; that is, subject...
In the planning phase of clinical trials there is often considerable uncertainty regarding the size ...
Blinding is a methodologic safeguard of treatment evaluation, yet severely understudied empirically....
Objectives: To explore the theoretical justification for blinding in randomized trials and make reco...
Aims During phase I study conduct, blinded data are reviewed to predict the safety of increasing the...