Interpretating and reporting clinical trials: a guide to the CONSORT statement and the principles of randomised controlled trials
Gespeichert in:
| Format: | Buch |
|---|---|
| Sprache: | English |
| Veröffentlicht: |
Pyrmont, NSW
Australasian Med. Publ.
2007
|
| Ausgabe: | 1. publ. |
| Schlagworte: | |
| Online-Zugang: | Inhaltsverzeichnis |
| Beschreibung: | IX, 181 S. Ill., graph. Darst. |
| ISBN: | 9780977578641 097757864X |
Internformat
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| 245 | 1 | 0 | |a Interpretating and reporting clinical trials |b a guide to the CONSORT statement and the principles of randomised controlled trials |c Anthony Keech ; Val Gebski ; Rhana Pike |
| 246 | 1 | 3 | |a Clinical trials |
| 250 | |a 1. publ. | ||
| 264 | 1 | |a Pyrmont, NSW |b Australasian Med. Publ. |c 2007 | |
| 300 | |a IX, 181 S. |b Ill., graph. Darst. | ||
| 336 | |b txt |2 rdacontent | ||
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| 338 | |b nc |2 rdacarrier | ||
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| 700 | 1 | |a Keech, Anthony C. |e Sonstige |4 oth | |
| 700 | 1 | |a Gebski, Val J. |e Sonstige |4 oth | |
| 700 | 1 | |a Pike, Rhana |e Sonstige |4 oth | |
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| 999 | |a oai:aleph.bib-bvb.de:BVB01-016149437 | ||
Datensatz im Suchindex
| _version_ | 1804137184501956608 |
|---|---|
| adam_text | Contents
Foreword
....................................................................
iii
The authors
....................................................................
v
Acknowledgements
.............................................................
vi
The CONSORT statement
.......................................................viii
1
Randomised controlled trials: elements of a good study
.................................1
2
Introducing the report of a randomised controlled trial:
the title, abstract, scientific background and rationale
....................................8
3
Selecting participants for clinical trials
.............................................11
4
Specifying interventions in a clinical trial
...........................................16
5
Specifying objectives and outcomes for clinical trials
..................................21
6
Determining the sample size in a clinical trial
........................................28
7
Managing the resource demands of a large sample size in clinical trials:
can you succeed with fewer subjects?
..............................................39
8
Randomisation in clinical trials
................................................... 46
9
Allocation concealment and blinding: when ignorance is bliss
............................54
10
Statistical methods in clinical trials
.................................................65
11
Flow of participants in randomised studies
..........................................72
12
Recruitment to randomised studies
................................................79
13
Baseline data in clinical trials
.....................................................86
14
Inclusion of patients in clinical trial analysis: the intention-to-treat principle
.................92
15
Making sense of trial results: outcomes and estimation
.................................99
16
Subgroup analysis in clinical trials
................................................105
17
Applying subgroup analysis to individual patient decisions
.............................114
18
Multiple analyses in clinical trials: sound science or data dredging?
......................123
19
Balancing the outcomes: reporting harms (adverse events)
.............................132
20
Interpreting the results of a clinical trial
............................................143
21
Generalising the results of trials to clinical practice
...................................149
22
Putting results of a clinical trial into perspective
.....................................154
Glossary
....................................................................162
Index
......................................................................159
VII
|
| adam_txt |
Contents
Foreword
.
iii
The authors
.
v
Acknowledgements
.
vi
The CONSORT statement
.viii
1
Randomised controlled trials: elements of a good study
.1
2
Introducing the report of a randomised controlled trial:
the title, abstract, scientific background and rationale
.8
3
Selecting participants for clinical trials
.11
4
Specifying interventions in a clinical trial
.16
5
Specifying objectives and outcomes for clinical trials
.21
6
Determining the sample size in a clinical trial
.28
7
Managing the resource demands of a large sample size in clinical trials:
can you succeed with fewer subjects?
.39
8
Randomisation in clinical trials
. 46
9
Allocation concealment and blinding: when ignorance is bliss
.54
10
Statistical methods in clinical trials
.65
11
Flow of participants in randomised studies
.72
12
Recruitment to randomised studies
.79
13
Baseline data in clinical trials
.86
14
Inclusion of patients in clinical trial analysis: the intention-to-treat principle
.92
15
Making sense of trial results: outcomes and estimation
.99
16
Subgroup analysis in clinical trials
.105
17
Applying subgroup analysis to individual patient decisions
.114
18
Multiple analyses in clinical trials: sound science or data dredging?
.123
19
Balancing the outcomes: reporting harms (adverse events)
.132
20
Interpreting the results of a clinical trial
.143
21
Generalising the results of trials to clinical practice
.149
22
Putting results of a clinical trial into perspective
.154
Glossary
.162
Index
.159
VII |
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| illustrated | Illustrated |
| index_date | 2024-07-02T18:59:23Z |
| indexdate | 2024-07-09T21:08:16Z |
| institution | BVB |
| isbn | 9780977578641 097757864X |
| language | English |
| oai_aleph_id | oai:aleph.bib-bvb.de:BVB01-016149437 |
| oclc_num | 633337900 |
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| owner_facet | DE-355 DE-BY-UBR |
| physical | IX, 181 S. Ill., graph. Darst. |
| publishDate | 2007 |
| publishDateSearch | 2007 |
| publishDateSort | 2007 |
| publisher | Australasian Med. Publ. |
| record_format | marc |
| spelling | Interpretating and reporting clinical trials a guide to the CONSORT statement and the principles of randomised controlled trials Anthony Keech ; Val Gebski ; Rhana Pike Clinical trials 1. publ. Pyrmont, NSW Australasian Med. Publ. 2007 IX, 181 S. Ill., graph. Darst. txt rdacontent n rdamedia nc rdacarrier Klinisches Experiment (DE-588)4164223-5 gnd rswk-swf Klinisches Experiment (DE-588)4164223-5 s DE-604 Keech, Anthony C. Sonstige oth Gebski, Val J. Sonstige oth Pike, Rhana Sonstige oth Digitalisierung UB Regensburg application/pdf http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=016149437&sequence=000002&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA Inhaltsverzeichnis |
| spellingShingle | Interpretating and reporting clinical trials a guide to the CONSORT statement and the principles of randomised controlled trials Klinisches Experiment (DE-588)4164223-5 gnd |
| subject_GND | (DE-588)4164223-5 |
| title | Interpretating and reporting clinical trials a guide to the CONSORT statement and the principles of randomised controlled trials |
| title_alt | Clinical trials |
| title_auth | Interpretating and reporting clinical trials a guide to the CONSORT statement and the principles of randomised controlled trials |
| title_exact_search | Interpretating and reporting clinical trials a guide to the CONSORT statement and the principles of randomised controlled trials |
| title_exact_search_txtP | Interpretating and reporting clinical trials a guide to the CONSORT statement and the principles of randomised controlled trials |
| title_full | Interpretating and reporting clinical trials a guide to the CONSORT statement and the principles of randomised controlled trials Anthony Keech ; Val Gebski ; Rhana Pike |
| title_fullStr | Interpretating and reporting clinical trials a guide to the CONSORT statement and the principles of randomised controlled trials Anthony Keech ; Val Gebski ; Rhana Pike |
| title_full_unstemmed | Interpretating and reporting clinical trials a guide to the CONSORT statement and the principles of randomised controlled trials Anthony Keech ; Val Gebski ; Rhana Pike |
| title_short | Interpretating and reporting clinical trials |
| title_sort | interpretating and reporting clinical trials a guide to the consort statement and the principles of randomised controlled trials |
| title_sub | a guide to the CONSORT statement and the principles of randomised controlled trials |
| topic | Klinisches Experiment (DE-588)4164223-5 gnd |
| topic_facet | Klinisches Experiment |
| url | http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=016149437&sequence=000002&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA |
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