-
4
-
-
0024845507
-
The performance of the two-stage analysis of two-treatment, two-period cross-over trials
-
Freeman PR. The performance of the two-stage analysis of two-treatment, two-period cross-over trials. Statistics in Medicine 1989; 8:1421-1432.
-
(1989)
Statistics in Medicine
, vol.8
, pp. 1421-1432
-
-
Freeman, P.R.1
-
5
-
-
0030864786
-
Use of two-stage test statistics in the two-period crossover trials
-
Wang SJ, Hung HMJ. Use of two-stage test statistics in the two-period crossover trials. Biometrics 1997; 53:1081-1091.
-
(1997)
Biometrics
, vol.53
, pp. 1081-1091
-
-
Wang, S.J.1
Hung, H.M.J.2
-
6
-
-
0003922013
-
-
United States Food and Drug Administration. U.S. Department of Health and Human Services Food and Drug Administration Center for Drug Evaluation and Research (CDER). Accessed January
-
United States Food and Drug Administration. Guidance for Industry: Statistical Approaches to Establishing Bioequivalence. U.S. Department of Health and Human Services Food and Drug Administration Center for Drug Evaluation and Research (CDER). Accessed January 2001 http://www.fda.gov/cder/guidance/3616fnl.htm#P353_2704.
-
(2001)
Guidance for Industry: Statistical Approaches to Establishing Bioequivalence
-
-
-
7
-
-
0027054784
-
Investigation of dual-balanced crossover designs for two treatments
-
Carriere KC, Reinsel GC. Investigation of dual-balanced crossover designs for two treatments. Biometrics 1992; 48:1157-1164.
-
(1992)
Biometrics
, vol.48
, pp. 1157-1164
-
-
Carriere, K.C.1
Reinsel, G.C.2
-
8
-
-
0036212092
-
Randomized, placebo-controlled, parallel group versus crossover study designs for the study of dementia in Parkinson's disease
-
Putt ME, Ravina B. Randomized, placebo-controlled, parallel group versus crossover study designs for the study of dementia in Parkinson's disease. Controlled Clinical Trials 2002; 23:111-126.
-
(2002)
Controlled Clinical Trials
, vol.23
, pp. 111-126
-
-
Putt, M.E.1
Ravina, B.2
-
9
-
-
11344260005
-
Efficiency of the cross-over design: An empirical estimation
-
Garcia R, Benet M, Arnau C, Cobo E. Efficiency of the cross-over design: an empirical estimation. Statistics in Medicine 2004; 23:3773-3780.
-
(2004)
Statistics in Medicine
, vol.23
, pp. 3773-3780
-
-
Garcia, R.1
Benet, M.2
Arnau, C.3
Cobo, E.4
-
10
-
-
0037905488
-
Clinical trials and rare disease
-
Lagakos S. Clinical trials and rare disease. New England Journal of Medicine 2003; 384:2455-2456.
-
(2003)
New England Journal of Medicine
, vol.384
, pp. 2455-2456
-
-
Lagakos, S.1
-
11
-
-
0031936729
-
A review of the randomized controlled trials of tacrine in the treatment of Alzheimer's disease: Methodologic considerations
-
Conway E. A review of the randomized controlled trials of tacrine in the treatment of Alzheimer's disease: methodologic considerations. Clinical Neuropharmacology 1998; 21:8-17.
-
(1998)
Clinical Neuropharmacology
, vol.21
, pp. 8-17
-
-
Conway, E.1
-
12
-
-
0018987266
-
The cross-over experiment for clinical trials
-
Brown B. The cross-over experiment for clinical trials. Biometrics 1980; 36:69-79.
-
(1980)
Biometrics
, vol.36
, pp. 69-79
-
-
Brown, B.1
-
13
-
-
70449541670
-
The two-period change over design and its use in clinical trials
-
Grizzle JE. The two-period change over design and its use in clinical trials. Biometrics 1965; 21:467-480.
-
(1965)
Biometrics
, vol.21
, pp. 467-480
-
-
Grizzle, J.E.1
-
14
-
-
0043043617
-
Correction to Grizzle
-
Grizzle JE. Correction to Grizzle. Biometrics 1974; 30:727.
-
(1974)
Biometrics
, vol.30
, pp. 727
-
-
Grizzle, J.E.1
-
16
-
-
10644257506
-
Carry-over in cross-over trials in bioequivalence: Theoretical concerns and empirical evidence
-
Senn SG, D'Angelo G, Potvin D. Carry-over in cross-over trials in bioequivalence: theoretical concerns and empirical evidence. Pharmaceutical Statistics 2004; 3:133-142.
-
(2004)
Pharmaceutical Statistics
, vol.3
, pp. 133-142
-
-
Senn, S.G.1
D'Angelo, G.2
Potvin, D.3
-
17
-
-
0037102906
-
Meta-analysis combining parallel and cross-over clinical trials. I: Continuous outcomes
-
Curtin F, Altman DG, Elbourne D. Meta-analysis combining parallel and cross-over clinical trials. I: continuous outcomes. Statistics in Medicine 2002; 21:2131-2144.
-
(2002)
Statistics in Medicine
, vol.21
, pp. 2131-2144
-
-
Curtin, F.1
Altman, D.G.2
Elbourne, D.3
-
18
-
-
0037102913
-
Meta-analysis combining parallel and cross-over clinical trials. III: The issue of carry-over
-
Curtin F, Elbourne DG, Altman D. Meta-analysis combining parallel and cross-over clinical trials. III: the issue of carry-over. Statistics in Medicine 2002; 21:2161-2173.
-
(2002)
Statistics in Medicine
, vol.21
, pp. 2161-2173
-
-
Curtin, F.1
Elbourne, D.G.2
Altman, D.3
-
19
-
-
0036211922
-
Meta-analyses involving cross-over trials: Methodological issues
-
Elbourne DR, Altman DG, Higgins, Curtin F, Worthington H, Vail A. Meta-analyses involving cross-over trials: methodological issues. International Journal of Epidemiology 2002; 31:140-149.
-
(2002)
International Journal of Epidemiology
, vol.31
, pp. 140-149
-
-
Elbourne, D.R.1
Altman, D.G.2
Higgins3
Curtin, F.4
Worthington, H.5
Vail, A.6
-
20
-
-
0035482259
-
Asthma stability after oral prednisone
-
Ahrens RC, Teresi ME, Han S, Donnell D, Vanden Burgt J, Lux CR. Asthma stability after oral prednisone. Respiratory and Critical Care Medicine 2001; 164:1138-1145.
-
(2001)
Respiratory and Critical Care Medicine
, vol.164
, pp. 1138-1145
-
-
Ahrens, R.C.1
Teresi, M.E.2
Han, S.3
Donnell, D.4
Vanden Burgt, J.5
Lux, C.R.6
-
21
-
-
0036357522
-
Inhaled beclomethasone versus budesonide for chronic asthma
-
(Cochrane Review) Wiley: Chichester, U.K
-
Bestall N, Jones PW. Inhaled beclomethasone versus budesonide for chronic asthma (Cochrane Review). The Cochrane Library 2003; Issue 4. Wiley: Chichester, U.K.
-
(2003)
The Cochrane Library
, Issue.4
-
-
Bestall, N.1
Jones, P.W.2
-
22
-
-
0030950122
-
The behavior of the p-value when the alternative hypothesis is true
-
Hung HM, O'Neill R, Bauer P, Kohne K. The behavior of the p-value when the alternative hypothesis is true. Biometrics 1997; 53:11-22.
-
(1997)
Biometrics
, vol.53
, pp. 11-22
-
-
Hung, H.M.1
O'Neill, R.2
Bauer, P.3
Kohne, K.4
-
23
-
-
1842607847
-
R: A language and environment for statistical computing
-
Development Core Team. R Foundation for Statistical Computing: Vienna, Austria. ISBN 3-900051-00-3
-
Development Core Team. R: a language and environment for statistical computing. R Foundation for Statistical Computing: Vienna, Austria. ISBN 3-900051-00-3. http:www.R-project.org.
-
-
-
-
24
-
-
0023615056
-
A comparison of the two one-sided tests procedure and the power approach for assessing the equivalence of average bioavailability
-
Schuirmann DJ. A comparison of the two one-sided tests procedure and the power approach for assessing the equivalence of average bioavailability. Journal of Pharmacokinetics and Biopharmaceutics 1987; 15:657-680.
-
(1987)
Journal of Pharmacokinetics and Biopharmaceutics
, vol.15
, pp. 657-680
-
-
Schuirmann, D.J.1
-
25
-
-
0000767465
-
A nonparametric approach to the analysis of three-treatment three-period crossover designs
-
Bellavance F, Tardif S. A nonparametric approach to the analysis of three-treatment three-period crossover designs. Biometrika 82:865-875.
-
Biometrika
, vol.82
, pp. 865-875
-
-
Bellavance, F.1
Tardif, S.2
-
27
-
-
0027244039
-
On population and individual bioequivalence
-
Schall R, Luus HG. On population and individual bioequivalence. Statistics in Medicine 1993; 12:1109-1124.
-
(1993)
Statistics in Medicine
, vol.12
, pp. 1109-1124
-
-
Schall, R.1
Luus, H.G.2
-
28
-
-
0026711141
-
On power calculation of Schuirmann's two one-sided tests procedure in bioequivalence
-
Liu JP, Chow SC. On power calculation of Schuirmann's two one-sided tests procedure in bioequivalence. Journal of Pharmacokinetics and Biopharmaceutics 1992; 20:101-104.
-
(1992)
Journal of Pharmacokinetics and Biopharmaceutics
, vol.20
, pp. 101-104
-
-
Liu, J.P.1
Chow, S.C.2
|