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Volumn 26, Issue 4, 2003, Pages 404-414

Toward rapproachment in the placebo control debate: A Calculated Compromise of Power

Author keywords

Clinical trial; Placebo; Power analysis; Sample size

Indexed keywords

PLACEBO;

EID: 0242641574     PISSN: 01632787     EISSN: None     Source Type: Journal    
DOI: 10.1177/0163278703258106     Document Type: Article
Times cited : (8)

References (19)
  • 4
    • 0022588960 scopus 로고
    • Scientific and ethical considerations in the use of placebo controls in clinical trials in psychopharmacology
    • Klerman, G. L. (1986). Scientific and ethical considerations in the use of placebo controls in clinical trials in psychopharmacology. Psychopharmacology Bulletin, 22, 25-29.
    • (1986) Psychopharmacology Bulletin , vol.22 , pp. 25-29
    • Klerman, G.L.1
  • 6
    • 0022608794 scopus 로고
    • The placebo control in clinical trials (a view from the FDA)
    • Leber, P. D. (1986). The placebo control in clinical trials (a view from the FDA). Psychopharmacology Bulletin, 22, 30-32.
    • (1986) Psychopharmacology Bulletin , vol.22 , pp. 30-32
    • Leber, P.D.1
  • 7
    • 0024443991 scopus 로고
    • The hazards of inference: The active control investigation
    • Leber, P. D. (1986). The hazards of inference: The active control investigation. Epilepsia, 30, S57-S63.
    • (1986) Epilepsia , vol.30
    • Leber, P.D.1
  • 8
    • 0035003398 scopus 로고    scopus 로고
    • Placebo controls can reduce exposure to risk: A power analytic perspective
    • Leon, A. C. (2001). Placebo controls can reduce exposure to risk: A power analytic perspective. Clinical Therapeutics, 23, 596-603.
    • (2001) Clinical Therapeutics , vol.23 , pp. 596-603
    • Leon, A.C.1
  • 10
    • 0242505454 scopus 로고    scopus 로고
    • Office for Protection From Research Risks, Department of Health and Human Services, National Institutes of Health. Code of Federal Regulations, DHHS 45, CFR 46, Part 46.111, Protection Of Human Participants. Revised November 13, 2001
    • Office for Protection From Research Risks, Department of Health and Human Services, National Institutes of Health. Code of Federal Regulations, DHHS 45, CFR 46, Part 46.111, Protection Of Human Participants. Revised November 13, 2001.
  • 11
    • 0036208659 scopus 로고    scopus 로고
    • Research on informed consent: Investigator-developed versus focus group developed consent documents, a VA cooperative study
    • Peduzzi, P., Guarino, P., Donta, S. T., Engel, C. C., Clauw, D. J., & Feussner, J. R. (2002). Research on informed consent: Investigator-developed versus focus group developed consent documents, a VA cooperative study. Controlled Clinical Trials, 23, 184-197.
    • (2002) Controlled Clinical Trials , vol.23 , pp. 184-197
    • Peduzzi, P.1    Guarino, P.2    Donta, S.T.3    Engel, C.C.4    Clauw, D.J.5    Feussner, J.R.6
  • 13
  • 16
    • 0034687072 scopus 로고    scopus 로고
    • Ptacebo-controtted trials and active-control trials in the evaluation of new treatments. Part 1: Ethical and scientific issues
    • Temple, R., & Etlenberg, S. S. (2000). Ptacebo-controtted trials and active-control trials in the evaluation of new treatments. Part 1: Ethical and scientific issues. Annals of Internal Medicine, 133, 455-463.
    • (2000) Annals of Internal Medicine , vol.133 , pp. 455-463
    • Temple, R.1    Etlenberg, S.S.2
  • 17
    • 0242389364 scopus 로고    scopus 로고
    • September
    • U.S. Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research, Center for Biologics Evaluation and Research. (1998, September). Guidance for industry: E9 statistical principles for clinical trials.
    • (1998) Guidance for Industry: E9 Statistical Principles for Clinical Trials


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.