A conceptual framework for clinical trials in SLE and other multisystem diseases
Identifieur interne : 002704 ( Main/Exploration ); précédent : 002703; suivant : 002705A conceptual framework for clinical trials in SLE and other multisystem diseases
Auteurs : Matthew H. Liang ; Michael Corzillius ; Sang-Cheol Bae ; Paul Fortin ; John M. Esdaile ; Michal Abrahamowicz [Canada]Source :
- Lupus [ 0961-2033 ] ; 1999-10.
English descriptors
- Teeft :
- Active control equivalence studies, Active disease, Activity measure, Adequate power, Adverse effects, Alternative hypothesis, Arch neurol, Ares, Arthritis, Arthritis rheum, Arthritis society, Autoimmune diseases, Autoimmune disorders, Baillieres clin rheumatol, Chronic pain, Clin, Clin epidemiol, Clinical manifestations, Clinical trial, Clinical trials, Combination therapy, Conceptual framework, Congestive heart failure, Control clin trials, Cutaneous manifestations, Disease activity, Dos, Effectiveness trials, Eligibility criteria, Eligible patients, Endpoint, Entry criteria, Equivalence, Equivalence hypothesis, Equivalence trial, Equivalence trials, Erythematosus, Exclusion criteria, Experimental treatment, Fatigue severity scale, Generic measures, Health status, Homogeneous population, Impairment, Important difference, Individual patients, Induction trials, Liang, Lupus, Lupus erythematosus, Lupus manifestations, Lupus nephritis, Maintenance trials, Major change, Manifestation, Meaningful change, More drugs, Multiple organ systems, Multiple sclerosis, Null hypothesis, Organ damage, Organ involvement, Organ system, Other diseases, Other hand, Outcome measures, Parallel approach, Partial remission, Physiologic health, Placebo, Primary endpoint, Proportional hazards model, Rand corporation, Randomized, Relapse, Remission, Renal disease, Respiratory hazards, Response criteria, Response criterion, Rheumatoid arthritis, Sample size, Sample size calculations, Sample size estimates, Sample size formulae, Santa monica, Severe disease, Simulation study, Single organ, Standard therapy, Standard treatment, Statist assoc, Statistical power, Steroid, Study agent, Study question, Such cases, Such changes, Systemic, Systemic lupus erythematosus, Treatment effect, True difference, Vascular disease.
Url:
DOI: 10.1191/096120399680411290
Affiliations:
Links toward previous steps (curation, corpus...)
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Le document en format XML
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<term>Active disease</term>
<term>Activity measure</term>
<term>Adequate power</term>
<term>Adverse effects</term>
<term>Alternative hypothesis</term>
<term>Arch neurol</term>
<term>Ares</term>
<term>Arthritis</term>
<term>Arthritis rheum</term>
<term>Arthritis society</term>
<term>Autoimmune diseases</term>
<term>Autoimmune disorders</term>
<term>Baillieres clin rheumatol</term>
<term>Chronic pain</term>
<term>Clin</term>
<term>Clin epidemiol</term>
<term>Clinical manifestations</term>
<term>Clinical trial</term>
<term>Clinical trials</term>
<term>Combination therapy</term>
<term>Conceptual framework</term>
<term>Congestive heart failure</term>
<term>Control clin trials</term>
<term>Cutaneous manifestations</term>
<term>Disease activity</term>
<term>Dos</term>
<term>Effectiveness trials</term>
<term>Eligibility criteria</term>
<term>Eligible patients</term>
<term>Endpoint</term>
<term>Entry criteria</term>
<term>Equivalence</term>
<term>Equivalence hypothesis</term>
<term>Equivalence trial</term>
<term>Equivalence trials</term>
<term>Erythematosus</term>
<term>Exclusion criteria</term>
<term>Experimental treatment</term>
<term>Fatigue severity scale</term>
<term>Generic measures</term>
<term>Health status</term>
<term>Homogeneous population</term>
<term>Impairment</term>
<term>Important difference</term>
<term>Individual patients</term>
<term>Induction trials</term>
<term>Liang</term>
<term>Lupus</term>
<term>Lupus erythematosus</term>
<term>Lupus manifestations</term>
<term>Lupus nephritis</term>
<term>Maintenance trials</term>
<term>Major change</term>
<term>Manifestation</term>
<term>Meaningful change</term>
<term>More drugs</term>
<term>Multiple organ systems</term>
<term>Multiple sclerosis</term>
<term>Null hypothesis</term>
<term>Organ damage</term>
<term>Organ involvement</term>
<term>Organ system</term>
<term>Other diseases</term>
<term>Other hand</term>
<term>Outcome measures</term>
<term>Parallel approach</term>
<term>Partial remission</term>
<term>Physiologic health</term>
<term>Placebo</term>
<term>Primary endpoint</term>
<term>Proportional hazards model</term>
<term>Rand corporation</term>
<term>Randomized</term>
<term>Relapse</term>
<term>Remission</term>
<term>Renal disease</term>
<term>Respiratory hazards</term>
<term>Response criteria</term>
<term>Response criterion</term>
<term>Rheumatoid arthritis</term>
<term>Sample size</term>
<term>Sample size calculations</term>
<term>Sample size estimates</term>
<term>Sample size formulae</term>
<term>Santa monica</term>
<term>Severe disease</term>
<term>Simulation study</term>
<term>Single organ</term>
<term>Standard therapy</term>
<term>Standard treatment</term>
<term>Statist assoc</term>
<term>Statistical power</term>
<term>Steroid</term>
<term>Study agent</term>
<term>Study question</term>
<term>Such cases</term>
<term>Such changes</term>
<term>Systemic</term>
<term>Systemic lupus erythematosus</term>
<term>Treatment effect</term>
<term>True difference</term>
<term>Vascular disease</term>
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