Placebo effect model in asthma clinical studies: longitudinal meta-analysis of forced expiratory volume in 1 second

Objective Our objective was to describe the time course of the placebo effect in asthma and quantitatively investigate the affective factors of the placebo effect for the placebo response simulation during the asthma clinical study design. Methods We conducted a systemic search of public data source...

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Published in:European journal of clinical pharmacology Vol. 68; no. 8; pp. 1157 - 1166
Main Authors: Wang, Xipei, Shang, Dewei, Ribbing, Jakob, Ren, Yupeng, Deng, Chenhui, Zhou, Tianyan, Guo, Feng, Lu, Wei
Format: Journal Article
Language:English
Published: Berlin/Heidelberg Springer-Verlag 01-08-2012
Springer
Springer Nature B.V
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Summary:Objective Our objective was to describe the time course of the placebo effect in asthma and quantitatively investigate the affective factors of the placebo effect for the placebo response simulation during the asthma clinical study design. Methods We conducted a systemic search of public data sources for the study-level forced expiratory volume in 1 second (FEV 1 ) to build the placebo effect model for studies by oral or inhaled administrations simultaneously. The administration routes, types of inhalation device, mean patient age, mean male proportion, baseline FEV 1 , disease severity, year of publication, inhaled corticosteroid status during the treatment, and dropout rate were tested as covariates. Results There are 34 literature sources containing 178 mean values for FEV 1 presenting the individual observations from about 3,703 patients. The exponential models adequately described the time course of placebo effect with the typical value of the maximum placebo effect (P max ) of 0.060 L. Dropout rate incorporated in the residual error model and the disease severity (mild to moderate and moderate to severe) at baseline were covariates that remained in the final model. Conclusions The placebo effect is adequately described by an exponential model over time. By incorporating the dropout rate in the residual error model, the estimation precision was improved. The model could predict the placebo response profile in mild to severe asthmatic patients for the asthma clinical study design and could also be a structure model of the placebo effect for the pure drug effect evaluation in the asthma clinical trials.
Bibliography:ObjectType-Article-2
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content type line 23
ISSN:0031-6970
1432-1041
DOI:10.1007/s00228-012-1245-2