nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
A group sequential adaptive treatment assignment design for proof of concept and dose selection in headache trials
|
Hall, David B. |
|
2005 |
26 |
3 |
p. 349-364 16 p. |
artikel |
2 |
An analysis of U.S. practices of paying research participants
|
Grady, Christine |
|
2005 |
26 |
3 |
p. 365-375 11 p. |
artikel |
3 |
A sensitivity analysis of a randomized controlled trial of zinc in treatment of falciparum malaria in children
|
Fox, Matthew P. |
|
2005 |
26 |
3 |
p. 281-289 9 p. |
artikel |
4 |
Can keeping clinical trial participants blind to their study treatment adversely affect subsequent care?
|
Blader, Joseph C. |
|
2005 |
26 |
3 |
p. 290-299 10 p. |
artikel |
5 |
Design and analysis of trials with rare outcomes: Examples from trials in herpes transmission and influenza prophylaxis
|
Keene, Oliver |
|
2005 |
26 |
3 |
p. 311-322 12 p. |
artikel |
6 |
Editorial Board
|
|
|
2005 |
26 |
3 |
p. iii- 1 p. |
artikel |
7 |
Effect of acyclovir on herpetic ocular recurrence using a structural nested model
|
Cole, Stephen R. |
|
2005 |
26 |
3 |
p. 300-310 11 p. |
artikel |
8 |
Estimating live birth rates after ovulation induction in polycystic ovary syndrome: Sample size calculations for the pregnancy in polycystic ovary syndrome trial
|
Myers, Evan R. |
|
2005 |
26 |
3 |
p. 271-280 10 p. |
artikel |
9 |
How to control measurement variation in estimating the mean intraocular pressure reducing effect at a specific point in time
|
Hedman, Katarina |
|
2005 |
26 |
3 |
p. 402-415 14 p. |
artikel |
10 |
Information for Authors
|
|
|
2005 |
26 |
3 |
p. I-II nvt p. |
artikel |
11 |
Letter from the Editors
|
|
|
2005 |
26 |
3 |
p. 269-270 2 p. |
artikel |
12 |
[No title]
|
Anderson, James R. |
|
2005 |
26 |
3 |
p. 416-417 2 p. |
artikel |
13 |
Practical applications of usability theory to electronic data collection for clinical trials
|
Schmier, Jordana K. |
|
2005 |
26 |
3 |
p. 376-385 10 p. |
artikel |
14 |
Psychotherapy in controlled psychopharmacology trials. Does it matter if we ignore it?
|
Koek, Ralph J. |
|
2005 |
26 |
3 |
p. 338-348 11 p. |
artikel |
15 |
Response to “The UCSD Statin Study: a randomized controlled trial assessing the impact of statins on selected noncardiac outcomes”
|
Antuono, Piero |
|
2005 |
26 |
3 |
p. 417-418 2 p. |
artikel |
16 |
Sample sizes for clinical trials with time-to-event endpoints and competing risks
|
Schulgen, Gabi |
|
2005 |
26 |
3 |
p. 386-396 11 p. |
artikel |
17 |
The effect of scientific misconduct on the results of clinical trials: A Delphi survey
|
Al-Marzouki, Sanaa |
|
2005 |
26 |
3 |
p. 331-337 7 p. |
artikel |
18 |
Trying to improve the compliance to colorectal cancer screening: A complex study design for a complex planning question
|
Giorgi Rossi, Paolo |
|
2005 |
26 |
3 |
p. 323-330 8 p. |
artikel |
19 |
Use of an embedded N-of-1 trial to improve adherence and increase information from a clinical study
|
Avins, Andrew L. |
|
2005 |
26 |
3 |
p. 397-401 5 p. |
artikel |