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                             60 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A comparison of data publication processes Roggenkamp, Katherine J.
 1980
 1 2 p. 169-170
2 p.
 artikel
2 A computer simulation study of methods of accounting for prognostic factors in clinical trials Pater, Joseph
 1980
 1 2 p. 174-175
2 p.
 artikel
3 Adaptive randomization biased coin design: Experience in a cooperative group clinical trial Hannigan Jr., John F.
 1980
 1 2 p. 175-
1 p.
 artikel
4 A generalized SAS procedure for the production and presentation of statistical tables Collins, Dorothea E.
 1980
 1 2 p. 170-
1 p.
 artikel
5 An efficient and flexible table producing program with statistics for monitoring a clinical trial Cross, Anne P.
 1980
 1 2 p. 169-
1 p.
 artikel
6 Assessment of staff interviewing and counseling skills for medication adherence in a clinical trial Russell, Michael L.
 1980
 1 2 p. 178-
1 p.
 artikel
7 A successful program for returning dropouts to a clinical trial Probstfield, Jeffrey L.
 1980
 1 2 p. 168-
1 p.
 artikel
8 A unique model for the development, conduct, and monitoring of clinical trials in a multi-hospital setting James, Kenneth E.
 1980
 1 2 p. 179-
1 p.
 artikel
9 Basic guidelines for institution data management in multi-center clinical trials McFadden, Eleanor
 1980
 1 2 p. 172-
1 p.
 artikel
10 Central case validation Cramer, Joyce A.
 1980
 1 2 p. 169-
1 p.
 artikel
11 Certification of clinics and staff in a multicenter clinical trial Rand, Lawrence I.
 1980
 1 2 p. 175-176
2 p.
 artikel
12 Choosing the best P value for clinical trials Dupont, William D.
 1980
 1 2 p. 171-
1 p.
 artikel
13 Collecting personnel-task-time data at a multicenter clinical trial coordinating center Knatterud, Genell L.
 1980
 1 2 p. 179-
1 p.
 artikel
14 Combined second annual scientific sessions of the society for clinical trials and Eighth annual symposium for coordinating clinical trials Klimt, Christian R.
 1980
 1 2 p. 188-
1 p.
 artikel
15 Conducting clinical trials with practicing community oncologists Murphy, James R.
 1980
 1 2 p. 180-
1 p.
 artikel
16 Controlled clinical trials and drug regulations Burkhardt, R.
 1980
 1 2 p. 153-166
14 p.
 artikel
17 Cooperative Crohn's disease study in Sweden—practical problems in planning and conducting multicenter trials Bergelin, Ingemar
 1980
 1 2 p. 178-
1 p.
 artikel
18 Coordinating a certification program for a multicenter clinical trial Hoskins, Joyce B.
 1980
 1 2 p. 175-
1 p.
 artikel
19 Coordinating activities of a national cooperative group program at a participating institution Ettinger, Nancy A.
 1980
 1 2 p. 172-
1 p.
 artikel
20 Corticosteroid trials in stroke: A critique Hachinski, Vladimir
 1980
 1 2 p. 177-
1 p.
 artikel
21 Critical comparisons of software Foulkes, Mary A.
 1980
 1 2 p. 173-
1 p.
 artikel
22 Crossover studies—Do the assumptions hold? Temkin, Nancy R.
 1980
 1 2 p. 167-
1 p.
 artikel
23 Data management training workshops as developed by the eastern cooperative oncology group Orlow, Erica L.
 1980
 1 2 p. 176-
1 p.
 artikel
24 Data monitoring at the national surgical adjuvant project for breast and bowel cancers (NSABP) Oleson, Charles E.
 1980
 1 2 p. 173-
1 p.
 artikel
25 Data quality control in a multi-insitutional cancer trial Koretz, M.M.
 1980
 1 2 p. 171-172
2 p.
 artikel
26 Design and implementation of a clinical trial of carcinoembryonic antigen as an indicator for second look surgery in colorectal cancer. A southwest oncology group study Young, Donn C.
 1980
 1 2 p. 174-
1 p.
 artikel
27 Diverse roles of data coordinators for small clinical studies Fox, Norma C.
 1980
 1 2 p. 178-
1 p.
 artikel
28 Effects of reporting lags on interim interferences from clinical trials Hanley, James
 1980
 1 2 p. 171-
1 p.
 artikel
29 Emergence of treatment associated subgroups in randomized therapeutic trials Chlebowski, R.T.
 1980
 1 2 p. 171-
1 p.
 artikel
30 Establishing minimal institutional patient entry rate requirements for participation in multicenter clinical trials Sylvester, R.J.
 1980
 1 2 p. 179-
1 p.
 artikel
31 Factors relating to collection and organization of family data Maciolowski, Marek
 1980
 1 2 p. 168-
1 p.
 artikel
32 Historical versus randomized controls for clinical trials Chalmers, Thomas C.
 1980
 1 2 p. 177-
1 p.
 artikel
33 How valid is disease-free survival as an endpoint in adjutant trials Carter, Stephen K.
 1980
 1 2 p. 177-178
2 p.
 artikel
34 Investigator initiated multi-center clinical trials and the national institutes of health Hollingsworth, Charles G.
 1980
 1 2 p. 179-180
2 p.
 artikel
35 Modelling recruitment from the population to the randomized patient Matts, John P.
 1980
 1 2 p. 169-
1 p.
 artikel
36 Multi-response logistic risk function in follow-up studies Elandt-Johnson, Regina C.
 1980
 1 2 p. 167-
1 p.
 artikel
37 Patient recruitment in VA cooperative studies Williford, William O.
 1980
 1 2 p. 168-
1 p.
 artikel
38 Patient registration in a cooperative oncology group Herson, Jay
 1980
 1 2 p. 101-110
10 p.
 artikel
39 Perceptions of the coordinating center Prout, Thaddeus E.
 1980
 1 2 p. 127-132
6 p.
 artikel
40 Perceptions of the coordinating center Berge, Kenneth G.
 1980
 1 2 p. 143-146
4 p.
 artikel
41 Perceptions of the coordinating center Lachin, John M.
 1980
 1 2 p. 125-126
2 p.
 artikel
42 Perceptions of the coordinating center Sedransk, N.
 1980
 1 2 p. 147-152
6 p.
 artikel
43 Perceptions of the coordinating center Rifkind, Basil M.
 1980
 1 2 p. 137-142
6 p.
 artikel
44 Perceptions of the coordinating center Overton, Hannah H.
 1980
 1 2 p. 133-136
4 p.
 artikel
45 Perusing the literature Hawkins, Barbara S.
 1980
 1 2 p. 181-186
6 p.
 artikel
46 Post-marketing surveillance of approved pharmaceuticals in the United States Nichol, F.Richard
 1980
 1 2 p. 178-
1 p.
 artikel
47 Producing the safety and data monitoring board report using SAS Pantelas, Sylvia G.
 1980
 1 2 p. 170-
1 p.
 artikel
48 Prognostic factors: Determination and role in design of clinical trials Stanley, Kenneth E.
 1980
 1 2 p. 174-
1 p.
 artikel
49 Protection of patient rights and welfare in the VA cooperative studies program Kathe, Barbara A.
 1980
 1 2 p. 173-174
2 p.
 artikel
50 Quality control of computerized data analysis in clinical trials Muller, Sally M.
 1980
 1 2 p. 173-
1 p.
 artikel
51 Review of protocol design in carcinoma of the head and neck (H & N) Poster, D.S.
 1980
 1 2 p. 176-
1 p.
 artikel
52 Sample sizes for long-term medical trial with time-dependent dropout and event rates Wu, Margaret
 1980
 1 2 p. 111-124
14 p.
 artikel
53 Society for clinical trials 1980
 1 2 p. 187-
1 p.
 artikel
54 Stopping rules for long-term clinical trials Taylor, D.W.
 1980
 1 2 p. 170-
1 p.
 artikel
55 Subjects and drugs suitable for crossover drug efficacy trials Scoville, B.
 1980
 1 2 p. 168-
1 p.
 artikel
56 Terminology—A plea for standardization Meinert, Curtis L.
 1980
 1 2 p. 97-100
4 p.
 artikel
57 The role of a central laboratory's local data management system in a multicenter study Moore, Patricia
 1980
 1 2 p. 172-
1 p.
 artikel
58 The trial assessment procedure scale Levine, Jerome
 1980
 1 2 p. 177-
1 p.
 artikel
59 Trends in clinical trials design Hopwood, Marsha D.
 1980
 1 2 p. 176-
1 p.
 artikel
60 Variations in national practices and their influences upon international research Thompson, Nancy J.
 1980
 1 2 p. 174-
1 p.
 artikel
                             60 gevonden resultaten
 
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