Fortschritte Der Arzneimittelforschung / Progress in Drug Research / Progrès Des Recherches Pharmaceutiques 1959
DOI: 10.1007/978-3-0348-7035-1_5
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Cited by 8 publications
(6 citation statements)
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“…At the end of 1960, Fleckenstein and Godfraind initiated experimental studies to alter calcium function in excitation-contraction coupling by pharmacological ligands in their laboratory. Haas and Hartfelder described verapamil in 1962 as a coronary vasodilator [3]. In 1967, Fleckenstein and Grun presented evidence that the vasodilating properties of verapamil were related to calcium antagonism.…”
Section: Introductionmentioning
confidence: 98%
“…At the end of 1960, Fleckenstein and Godfraind initiated experimental studies to alter calcium function in excitation-contraction coupling by pharmacological ligands in their laboratory. Haas and Hartfelder described verapamil in 1962 as a coronary vasodilator [3]. In 1967, Fleckenstein and Grun presented evidence that the vasodilating properties of verapamil were related to calcium antagonism.…”
Section: Introductionmentioning
confidence: 98%
“…In 1747, Lind was the first person to use a control medication. He wanted to demonstrate the efficacy of orange an d lemon juice in two scurvy sufferers by giving one patient a drink consisting of sea water and mustard and the other the "active treatment" [16]. In 1932, in his guide to methods of clinical research ["Methodenlehre der therapeutischen Untersuchung"], the founder of clinical pharmacology, Paul Martini, describes the use of dummy tablets (although without actually using the term "placebo" in this context) to objectify the effects of drugs in double-blind studies:…”
Section: History: Blind and Non-blind Use Of Placebos In Therapymentioning
confidence: 99%
“…The ethical and legal premises for using placebo are discussed critically and in detail in the literature (Heimchen and Mül/er-Oerlinghausen 1978;Müller-Oerlinghausen 1983;Müller-Oerlinghausen and Herrmann 1981), and are not the topic of this re port. The purpose of this report is to discuss problems related to the use of traditional placebo-controlled designs in clinical drug trials, and to discuss possible solutions to these problems (Binz 1977;Boume 1971;Haas et al 1959;Michaelis 1982;Netter 1977;Piechowiak 1981;Schindel 1978;Schindel 1967).…”
Section: Placebo-control/ed Trialsmentioning
confidence: 99%