Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Manjula Schou"'
Publikováno v:
Journal of Market Access & Health Policy, Vol 12, Iss 1, Pp 5-20 (2024)
The aim of this study was to evaluate the comparative clinical effectiveness and cost-utility of the active transcutaneous Osia® System versus the passive transcutaneous Baha® Attract System for patients with conductive or mixed hearing loss or sin
Externí odkaz:
https://doaj.org/article/a5628e3036e4427a8fd3d2f4394d78b5
Publikováno v:
Trials, Vol 21, Iss 1, Pp 1-8 (2020)
Abstract Background Despite careful planning, changes to some aspects of an ongoing randomised clinical trial (RCT), with a fixed design, may be warranted. We sought to elucidate the distinction between legitimate versus illegitimate changes to serve
Externí odkaz:
https://doaj.org/article/574a6f8467914e0e9faadb761df466b8
Publikováno v:
Kaohsiung Journal of Medical Sciences, Vol 26, Iss 10, Pp 532-539 (2010)
This study was carried out to obtain information on the efficacy and safety of the controlled release formulation of the doxazosin Gastrointestinal Therapeutic System (GITS) in Taiwanese subjects with benign prostatic hyperplasia (BPH). Studies of do
Externí odkaz:
https://doaj.org/article/5e8bfe3ffc6540dfa5fdc90b562dd4c4
Publikováno v:
Statistical Methods in Medical Research. 31:2456-2469
When a clinical trial stops early for benefit, the maximum likelihood estimate (MLE) of the treatment effect may be subject to overestimation bias. Several authors have proposed adjusting for this bias using the conditional MLE, which is obtained by
Autor:
Ian C Marschner, I Manjula Schou
Publikováno v:
Clinical Trials. 19:479-489
Background Adaptive platform trials allow randomized controlled comparisons of multiple treatments using a common infrastructure and the flexibility to adapt key design features during the study. Nonetheless, they have been criticized due to the pote
Autor:
I. Manjula Schou
Publikováno v:
The Journal of rheumatology. 49(9)
Publikováno v:
Research Synthesis Methods. 11:287-300
The CONSORT Statement says that data-driven early stopping of a clinical trial is likely to weaken the inferences that can be drawn from the trial. The GRADE guidelines go further, saying that early stopping is a study limitation that carries the ris
Publikováno v:
Contemporary clinical trials. 110
Clinical trialists may regard an observed imbalance on a prognostic covariate as sufficiently troubling to warrant action. Objective To elucidate the issues associated with selecting, and switching between, an unadjusted versus an adjusted analysis i
Publikováno v:
Trials
Trials, Vol 21, Iss 1, Pp 1-8 (2020)
Trials, Vol 21, Iss 1, Pp 1-8 (2020)
Background Despite careful planning, changes to some aspects of an ongoing randomised clinical trial (RCT), with a fixed design, may be warranted. We sought to elucidate the distinction between legitimate versus illegitimate changes to serve as a gui
Autor:
I. Manjula Schou, Ian C. Marschner
Publikováno v:
Biometrical Journal. 59:636-657
Randomized clinical trials comparing several treatments to a common control are often reported in the medical literature. For example, multiple experimental treatments may be compared with placebo, or in combination therapy trials, a combination ther