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                             116 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 Academic coordinating centers for industry-sponsored trials Fowler, Sarah
1998
19 3S1 p. S71-
1 p.
artikel
2 A case study in computer-assisted trial design: Innovative simulation techniques for clinical trials Weiner, Daniel
1998
19 3S1 p. S48-S49
2 p.
artikel
3 A centralized multi-disciplinary approach to determining specific cause of death Sunkle, Susan
1998
19 3S1 p. S99-
1 p.
artikel
4 A correction term for sample size estimation in cluster randomized studies with varying cluster size Manatunga, Amita K.
1998
19 3S1 p. S37-S38
2 p.
artikel
5 Adjusting the significance level of the final analysis with multiple interim analysis and fixed sample size Arulchelvam, I.M.
1998
19 3S1 p. S45-
1 p.
artikel
6 Agreement of data in abstracts compared to full publications Chokkalingam, Anand
1998
19 3S1 p. S61-S62
2 p.
artikel
7 Agreement on CDR ratings by committee Tractenberg, Rochelle
1998
19 3S1 p. S89-
1 p.
artikel
8 A method to identify the subgroup for whom treatment is most effective Lynn, Henry
1998
19 3S1 p. S66-S67
2 p.
artikel
9 A model for non-synchronized interval-censored data from the surveillance of tuberculosis infection in health care workers Wang, Yong-Cheng
1998
19 3S1 p. S55-S56
2 p.
artikel
10 Analysis and presentation of adverse experiences for interim monitoring Krause-Steinrauf, Heidei
1998
19 3S1 p. S44-
1 p.
artikel
11 Analysis of health status data with a large proportion of zeros Gillespie, Brenda W.
1998
19 3S1 p. S56-
1 p.
artikel
12 Analysis of multivariate failure time data in a clinical trials: Estimation of overall treatment effect and strength of correlation Mahe, Cédric
1998
19 3S1 p. S42-S43
2 p.
artikel
13 Analysis of survival by palliative response in patients with symptomatic hormone refractory prostate cancer Panzarella, Tony
1998
19 3S1 p. S77-
1 p.
artikel
14 Analyzing a continuous efficacy response in a long-term trial with high dropout rate Wang, Daniel Z.
1998
19 3S1 p. S66-
1 p.
artikel
15 Analyzing symptom and quality of life scores in clinical trials Zhang, Ji
1998
19 3S1 p. S80-
1 p.
artikel
16 An automated medical event tracking system Payne, Adam
1998
19 3S1 p. S95-
1 p.
artikel
17 An extranet for multi-center clinical trials Temprosa, Marinella
1998
19 3S1 p. S63-
1 p.
artikel
18 An instrument to assess the quality of randomised clinical trial protocols Ghersi, Davina
1998
19 3S1 p. S88-S89
2 p.
artikel
19 An integrated database information system for the veterans health study Levenson, Suzette M.
1998
19 3S1 p. S73-
1 p.
artikel
20 An issue of statistical analysis in controlled multicenter studies: How shall we weight the centers? Lin, Zhengning
1998
19 3S1 p. S54-
1 p.
artikel
21 An overview of group sequential methods in longitudinal clinical trials Spiessens, Bart
1998
19 3S1 p. S45-
1 p.
artikel
22 A passive intranet for viewing images, data, and documents at a multicenter trial coordinating center Grubb, Stephen C.
1998
19 3S1 p. S65-
1 p.
artikel
23 Appropriate coding systems for indexing clinical trials Strang, W. Nigel
1998
19 3S1 p. S62-
1 p.
artikel
24 A proposed evaluation algorithm for the heterogeneity of the baseline risk within patient populations of clinical trial Ioannidis, John P.A.
1998
19 3S1 p. S67-
1 p.
artikel
25 A review of statistical methods to differentiate a treatment effect for small shifts in the tail of a distribution Liu, Minzhi
1998
19 3S1 p. S68-
1 p.
artikel
26 A simple graphical method for displaying multiple dimensions by group over time: An example using the SF-36 Door, David A.
1998
19 3S1 p. S72-
1 p.
artikel
27 A simulation study of the effects of small center enrollment in multi-center clinical trials Thompson, Jaye
1998
19 3S1 p. S53-S54
2 p.
artikel
28 A systems for performing site visit audits in studies which involve healthy subjects Cronin, Walter M.
1998
19 3S1 p. S51-
1 p.
artikel
29 Author index 1998
19 3S1 p. S102-S113
12 p.
artikel
30 Balanced approach in clinical trial management (CTM) between modern technologies and practical realities Caldwell, Thomas
1998
19 3S1 p. S64-S65
2 p.
artikel
31 Breaking into databases: Interactive data entry on the web Bak, Sharon M.
1998
19 3S1 p. S64-
1 p.
artikel
32 Can routine data be used in conjuncture with randomised controlled trials? Lewsey, James
1998
19 3S1 p. S86-
1 p.
artikel
33 Categorization of a prognostic factor in a multivariable setting for a large critical care database Glassman, J.
1998
19 3S1 p. S93-
1 p.
artikel
34 Challenges in data collection in the Asian-Pacific region Ritchie, Gemma
1998
19 3S1 p. S83-
1 p.
artikel
35 Change in quality of life assessed with area under the curve method Pintilie, Melania
1998
19 3S1 p. S80-
1 p.
artikel
36 Clinical trials management project management systems: Do we need them? Humphreys, John
1998
19 3S1 p. S94-
1 p.
artikel
37 Contribution of condition-specific quality of life (QOL) measurement to SF-36 Gordon, Mae
1998
19 3S1 p. S57-
1 p.
artikel
38 Cox proportional hazard model with tied events vis-a-vis logistic regression when modeling dichotomous outcomes Hussein, M.
1998
19 3S1 p. S55-
1 p.
artikel
39 Database schema for representation of data and meta-data for a survey software system Goldstein, Robert B.
1998
19 3S1 p. S82-
1 p.
artikel
40 Demographic characteristics and quality of life factors among the participants of the breast cancer prevention trial Costantino, Joseph P.
1998
19 3S1 p. S59-
1 p.
artikel
41 Design of a natural medicine effectiveness study in a community health clinic Winget, Marcy
1998
19 3S1 p. S50-
1 p.
artikel
42 Design of equivalence studies: Facts and fantasies Sylvester, Richard
1998
19 3S1 p. S91-
1 p.
artikel
43 Determination of power and sample size for proving equivalence based on the ratio of two means for normally distributed data Kieser, Meinhard
1998
19 3S1 p. S37-
1 p.
artikel
44 Duration projection for equivalence clinical trials with survival endpoints Dongsheng, Tu
1998
19 3S1 p. S78-
1 p.
artikel
45 Dynamic measurement scale development for clinical trials in targeted populations Jin, Shelia
1998
19 3S1 p. S58-
1 p.
artikel
46 Early stopping for futility: Phenobarbital use in reducing the risk of early death or intraventricular hemorrhage in premature infants Verter, Joel
1998
19 3S1 p. S92-
1 p.
artikel
47 Effective data management using a novel modular SAS® application Gunraj, Nadia
1998
19 3S1 p. S73-S74
2 p.
artikel
48 Electronic monitoring of participant adherence in the NSABP breast cancer prevention trial (BSPT) Day, Richard
1998
19 3S1 p. S69-S70
2 p.
artikel
49 Estimating cut scores and the standard errors with clinical data Lin, Ting Hsiang
1998
19 3S1 p. S93-
1 p.
artikel
50 Estimating treatment effects in an unbalanced two period cross-over trial with poisson outcomes Lunn, A.D.
1998
19 3S1 p. S91-
1 p.
artikel
51 Estimation of treatment effect on an endpoint assessed with methods of heterogeneous sensitivity: Example of deep vein Boutitie, F.
1998
19 3S1 p. S49-
1 p.
artikel
52 Evaluating the economic efficiency of alternative pulmonary rehabilitation interventions: Collecting cost data Duren-Winfield, Vanessa
1998
19 3S1 p. S75-S76
2 p.
artikel
53 Expansion of an institutional quality control program at a comprehensive cancer center Templeton, Mary Agnes
1998
19 3S1 p. S101-
1 p.
artikel
54 Experiences of a biostatistical coordinating center for a network of low birth weight infant research studies Mele, Lisa
1998
19 3S1 p. S39-
1 p.
artikel
55 Follow-up plots for large data sets Wong, Emelita L.
1998
19 3S1 p. S84-
1 p.
artikel
56 Identification and prediction of responders to a therapy: A model and its preliminary application to actual data Wei, Li auJean-Pierre Boissel
1998
19 3S1 p. S42-
1 p.
artikel
57 Incorporating a data management help line into an effective data management resource system Marks, Linda D.
1998
19 3S1 p. S71-S72
2 p.
artikel
58 Issues in comparisons between meta-analyses and large trials Ioannidis, John P.A.
1998
19 3S1 p. S62-S63
2 p.
artikel
59 Issues of protocol modification after initiation of a large multi-center trial Verter, Joel
1998
19 3S1 p. S38-S39
2 p.
artikel
60 Is the isotropy hypothesis true in hypertension findings from the Indana project Boissel, Jean-Pierre
1998
19 3S1 p. S85-S86
2 p.
artikel
61 Long-term tracking of randomized comparison groups Rajab, M.H.
1998
19 3S1 p. S52-S53
2 p.
artikel
62 Make your database work harder and take the afternoon off - increasing accuracy and efficiency in data management Crocombe, Will
1998
19 3S1 p. S94-
1 p.
artikel
63 Management of clinical trials as an academic Management of clinical trials as an academic good clinical practice (GCP) Garty, Nira B.
1998
19 3S1 p. S88-
1 p.
artikel
64 Measuring cognitive progression in Alzheimer's disease Berg, Julie D.
1998
19 3S1 p. S57-S58
2 p.
artikel
65 Measuring quality of life and baseline findings from the collaborative initial glaucoma treatment study (CIGTS) Wren, Patricia A.
1998
19 3S1 p. S56-S57
2 p.
artikel
66 Modeling and simulation in the drug approval process Rubin, Donald B.
1998
19 3S1 p. S65-S66
2 p.
artikel
67 Monitoring endpoint-based interim analyses for large comparative clinical cancer trials Luo, Xiaolong
1998
19 3S1 p. S79-
1 p.
artikel
68 Patient recruitment in the antihypertensive and lipid-lowering treatment to prevent heart attack trial (allhat) Pressel, Sara
1998
19 3S1 p. S46-
1 p.
artikel
69 Potential bias in remote data entry Maupas, Jean
1998
19 3S1 p. S41-S42
2 p.
artikel
70 Power calculation for randomized start design Kean, Yin M.
1998
19 3S1 p. S38-
1 p.
artikel
71 Power, clinical and statistical significance of the search of interactions between treatment effect and patient profiles: A practical approach Gueyffier, François
1998
19 3S1 p. S90-
1 p.
artikel
72 Predictors of missed visits in longitudinal studies: The NHLBI growth and health study (NGHS) Similo, Shari
1998
19 3S1 p. S83-S84
2 p.
artikel
73 Processing of data forms using handprint recognition software: An accuracy analysis Grubb, Stephen C.
1998
19 3S1 p. S41-
1 p.
artikel
74 Pseudo-trials: A method to explore the effect model Boissel, Jean-Pierre
1998
19 3S1 p. S61-
1 p.
artikel
75 Quality control methods for telephone interviewing in randomized controlled trials Perlmutter, Donna L.
1998
19 3S1 p. S99-S100
2 p.
artikel
76 Randomizations on the web: A new alternative Lethen, Jan
1998
19 3S1 p. S63-S64
2 p.
artikel
77 Reasons for enrollment and continued participation in a longitudinal, observational study: The interstitial cystitis data base (ICDB) study experience Matthews-Cook, Yvonne
1998
19 3S1 p. S69-
1 p.
artikel
78 Recruitment experience from phase II cancer chemoprevention studies Weiss, Heidi L.
1998
19 3S1 p. S98-
1 p.
artikel
79 Recruitment of women with CHF into a large clinical trial: Barriers and strategies Wood, Jackie Clare
1998
19 3S1 p. S46-S47
2 p.
artikel
80 Recruitment strategies used in the medical therapy of prostatic symptoms (MTOPS) trial Burrows, Pamela K.
1998
19 3S1 p. S97-
1 p.
artikel
81 85% reduction in database development time using standardized case report form components Owens, Edie
1998
19 3S1 p. S40-
1 p.
artikel
82 Reliability of chalmers' scale to assess quality in meta-analysis Bérard, Anick
1998
19 3S1 p. S60-
1 p.
artikel
83 Running an international study — problems and solutions Phillips, Angela
1998
19 3S1 p. S70-S71
2 p.
artikel
84 Sample size determination for the two-stage design of a phase II cancer clinical trials with correlated unbalance binary endpoints Shyr, Yu
1998
19 3S1 p. S40-
1 p.
artikel
85 Sensitivity analyses of Q-twist model for interferon maintenance therapy in multiple myeloma Tong, Li
1998
19 3S1 p. S59-S60
2 p.
artikel
86 Sham treatments in clinical trials: A review of the literature Reynolds, Sandra M.
1998
19 3S1 p. S75-
1 p.
artikel
87 Should confidence intervals serve as a surrogate for the significance test? Borenstein, Michael
1998
19 3S1 p. S92-
1 p.
artikel
88 Site visit strategies to increase collaboration of the clinic, resource centers and coordinating center Morris, Patricia A.
1998
19 3S1 p. S51-
1 p.
artikel
89 Some extensions and applications of a bayesian strategy for monitoring multiple outcomes in clinical trials Thall, Peter F.
1998
19 3S1 p. S44-
1 p.
artikel
90 Sponsor charge-back method for site use of supplies and equipment Day, Denni
1998
19 3S1 p. S85-
1 p.
artikel
91 Statistical assessment of resources during the design of megatrials Peszek, Izabella
1998
19 3S1 p. S70-
1 p.
artikel
92 Statistical power for a long term survival trial for an elderly population Jiandong, Lu
1998
19 3S1 p. S77-S78
2 p.
artikel
93 Successful recruitment for a four-year dietary intervention: The polyp prevention trial Murphy, Patricia A.
1998
19 3S1 p. S47-
1 p.
artikel
94 Suspending enrollment in a two-stage phase II trial of AIDS Kaposi's Sarcoma patients Lee, J.
1998
19 3S1 p. S98-S99
2 p.
artikel
95 The benefits of a clinic-specific pilot test in a multicenter clinical trial Howard, Virginia J.
1998
19 3S1 p. S52-
1 p.
artikel
96 The collaborative initial glaucoma treatment study (CIGTS): Reasons for refusing to participate in a surgery vs. medicine trial Musch, David C.
1998
19 3S1 p. S96-
1 p.
artikel
97 The effect of censoring on a multivariate cox regression model comparing surgical and medical treatment for aortic disease patients Oprian, Charles
1998
19 3S1 p. S78-S79
2 p.
artikel
98 The effect of external events on a large double blind chemoprevention trial Rotmensz, Nicole
1998
19 3S1 p. S76-
1 p.
artikel
99 The impact of adding new clinical centers during the course of a clinical trial for a rare condition Hollick, Rosemary A.
1998
19 3S1 p. S68-
1 p.
artikel
100 The impact of legislative changes on acquired immunodeficiency syndrome drug development Arida, Aynur Ünalp
1998
19 3S1 p. S86-S87
2 p.
artikel
101 The impact of written information on outpatients' knowledge about and attitude towards randomized clinical trials Kj˦rgå, Lise Lotte
1998
19 3S1 p. S74-
1 p.
artikel
102 The importance of event rates for clinical site effects in multicenter trials Ioannidis, John P.A.
1998
19 3S1 p. S53-
1 p.
artikel
103 The performance of the dersimonian and laird method with non-normal random effects in meta-analysis Chang, Bei-Hung
1998
19 3S1 p. S60-S61
2 p.
artikel
104 The presentation of clinical research to patients Hilger, Jacqueline
1998
19 3S1 p. S87-
1 p.
artikel
105 The UGDP controversy: Analysis using likelihood methods Blume, Jeffrey D.
1998
19 3S1 p. S43-
1 p.
artikel
106 Training and certification of personnel in the vitamin intervention for stroke prevention study (VISP) Sides, Elizabeth
1998
19 3S1 p. S100-
1 p.
artikel
107 Training program for introduction to data management in oncology clinical trials Roach, Linda
1998
19 3S1 p. S87-S88
2 p.
artikel
108 (Under) estimating paper storage requirements for a multicenter clinical trial Fischbach, Ellen
1998
19 3S1 p. S84-
1 p.
artikel
109 Use of cumulative sum control schemes for monitoring recruitment in clinical trials Bingham, Stephen F.
1998
19 3S1 p. S50-
1 p.
artikel
110 Use of mass mail to recruit older men into a clinical trial for medical treatment of benign prostatic hyperplasia (BPH): The medical therapy of prostatic symptoms (MTOPS) trial Kusek, John W.
1998
19 3S1 p. S48-
1 p.
artikel
111 Use of the world wide web in data dissemination to central review committees Schafer, Kimberly A.
1998
19 3S1 p. S81-
1 p.
artikel
112 Using an in-house clinical research database to automatically generate data in ACES® output format for Theradex Lin, Kai-Hsiung
1998
19 3S1 p. S95-
1 p.
artikel
113 Using Harvard graphics® and an HP Designjet 650C/PS® plotter to produce large-format research poster presentations Abdellatif, Mazen
1998
19 3S1 p. S82-S83
2 p.
artikel
114 Using teleform and access to create a relational database through an automated data entry Ahn, Chul
1998
19 3S1 p. S81-
1 p.
artikel
115 What is the utility of eligibility checklist screening? Sears, Catherine
1998
19 3S1 p. S96-
1 p.
artikel
116 Zelen randomization: Attitudes of parents participating in a neonatal clinical trial Snowdon, Claire
1998
19 3S1 p. S74-S75
2 p.
artikel
                             116 gevonden resultaten
 
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