Reference:ICH ICH E9 Guideline 1998 III: Difference between revisions
From GxPlex
gxplex>GxPlexBot Import from GxPlex Excel |
Gxplex admin (talk | contribs) m 1 revision imported |
||
| (8 intermediate revisions by 4 users not shown) | |||
| Line 1: | Line 1: | ||
{{ | {{ReferenceData | ||
| | |has_document=Document:ICH ICH E9 Guideline 1998 | ||
| | |module=1 | ||
| | |unit=1.2.7 | ||
| | |scope=HM | ||
| | |doc_part=III | ||
| | |language=EN | ||
| | |entry_by=Florian Adragna | ||
|contributors= | |||
|tags=TAG-00055-Stu-ngs ++ TAG-00142-Mul-ent ++ TAG-00056-Bio-tik | |||
|tags_display=[[Glossary:TAG-00055-Stu-ngs|Study design]], [[Glossary:TAG-00142-Mul-ent|Multicentre trial]], [[Glossary:TAG-00056-Bio-tik|Biostatistics]] | |||
|comment=Trial design configurations: parallel, crossover, factorial | |||
|content=III. TRIAL DESIGN CONSIDERATIONS | |||
|- | |||
|- | |||
|- | |||
| | |||
| | |||
| | |||
III. TRIAL DESIGN CONSIDERATIONS | |||
3.1 Design Configuration | 3.1 Design Configuration | ||
3.1.1 Parallel Group Design | 3.1.1 Parallel Group Design | ||
| Line 67: | Line 34: | ||
3.6 Data Capture and Processing | 3.6 Data Capture and Processing | ||
[...] | [...] | ||
}} | |||
Latest revision as of 13:49, 16 July 2026
| Document information | |
|---|---|
| Reference | ICH ICH E9 Guideline 1998 |
| Validity area | ICH |
| Scope(s) | HM |
| Document name | ICH E9 Guideline |
| Version / Revision | 1998 |
| Status | Current |
| Document type | International guideline |
| Language(s) | EN |
| Description | STATISTICAL PRINCIPLES FOR CLINICAL TRIALS E9 |
| Official source | Official link |
| Restricted access | No |
| Submitted by | Florian Adragna |
| Contributors | |
| Reference Details | |
|---|---|
| Module | Module 1 — Unit 1.2.7 |
| Scope | HM |
| Document part | III |
| Language | EN |
| Original entry by | Florian Adragna |
| Contributors | |
| Tags | Study design, Multicentre trial, Biostatistics |
Content
III. TRIAL DESIGN CONSIDERATIONS 3.1 Design Configuration 3.1.1 Parallel Group Design […] 3.1.2 Crossover Design […] 3.1.3 Factorial Designs […] 3.2 Multicentre Trials […] 3.3 Type of Comparison 3.3.1 Trials to Show Superiority […] 3.3.2 Trials to Show Equivalence or Non-inferiority [...] 3.3.3 Trials to Show Dose-response Relationship [...] 3.4 Group Sequential Designs [...] 3.5 Sample Size [...] 3.6 Data Capture and Processing [...]