ID
29566
Beschreibung
Study ID: 104385 Clinical Study ID: RES104385 Study Title: A randomised double-blind two-period crossover study to investigate the effect of treatment with repeat doses of a PPAR gamma agonist on the allergen-induced late asthmatic response in subjects with mild asthma compared with repeat doses of placebo Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00318630 https://clinicaltrials.gov/ct2/show/NCT00318630 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 1 Study Recruitment Status: Completed Generic Name: rosiglitazone Trade Name: Avandia XR,Avandia; Rosiglitazone XR,Avandia XR,Avandia Study Indication: Asthma This ODM-file contains ECG Abnormalities Form Part 2.
Link
https://clinicaltrials.gov/ct2/show/NCT00318630
Stichworte
Versionen (1)
- 06.04.18 06.04.18 - Sarah Riepenhausen
Rechteinhaber
GlaxoSmithKline
Hochgeladen am
6. April 2018
DOI
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Lizenz
Creative Commons BY-NC 3.0
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GSK Influence of PPAR gamma agonist vs. Placebo on allergen-induced late asthmatic response NCT00318630
ECG Abnormalities Form Part 2
- StudyEvent: ODM
Beschreibung
Myocardial infarction
Alias
- UMLS CUI-1
- C0027051
Beschreibung
D 1 Report, if clinically significant.
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0155668
Beschreibung
D 2 Report, if clinically significant.
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0340293
Beschreibung
D 3 Report, if clinically significant.
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0340312
Beschreibung
D 4 Report, if clinically significant.
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0340319
Beschreibung
D 5 Report, if clinically significant.
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0340305
Beschreibung
D 6 Report, if clinically significant.
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0746727
Beschreibung
D 20 Report, if clinically significant.
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0542269
Beschreibung
D 98 Report, if clinically significant.
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0027051
- UMLS CUI [1,2]
- C0205394
Beschreibung
Other myocardial infarction
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0027051
- UMLS CUI [1,2]
- C0205394
- UMLS CUI [1,3]
- C0947611
Beschreibung
Depolarisation/Repolarisation, QRS-T
Alias
- UMLS CUI-1
- C0948857
- UMLS CUI-2
- C1331539
- UMLS CUI-3
- C0520880
- UMLS CUI-4
- C0438167
Beschreibung
D 7 Record, if clinically significant.
Datentyp
boolean
Alias
- UMLS CUI [1]
- C1112720
Beschreibung
D 19 Record, if clinically significant.
Datentyp
boolean
Alias
- UMLS CUI [1]
- C2346597
Beschreibung
D 8 Record, if clinically significant.
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0520886
Beschreibung
D 21 Record, if clinically significant.
Datentyp
boolean
Alias
- UMLS CUI [1]
- C2348119
Beschreibung
D 9 Record, if clinically significant.
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0520887
Beschreibung
D 10 Record, if clinically significant.
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0438169
Beschreibung
D 11 Record, if clinically significant.
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0520888
Beschreibung
D 12 Record, if clinically significant.
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0239242
Beschreibung
D 15 Record, if clinically significant.
Datentyp
boolean
Alias
- UMLS CUI [1]
- C2215959
Beschreibung
D 16 Record, if clinically significant.
Datentyp
boolean
Alias
- UMLS CUI [1]
- C2348639
Beschreibung
D 18 Record, if clinically significant.
Datentyp
boolean
Alias
- UMLS CUI [1]
- C2347367
Beschreibung
D 13 Record, if clinically significant.
Datentyp
boolean
Alias
- UMLS CUI [1]
- C2349945
Beschreibung
D 17 Record, if clinically significant.
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0520888
- UMLS CUI [1,2]
- C0429059
Beschreibung
D 99 Report, if clinically significant.
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0948857
- UMLS CUI [1,2]
- C0205394
Beschreibung
Other depolarisation/repolarisation
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0948857
- UMLS CUI [1,2]
- C0205394
- UMLS CUI [1,3]
- C0947611
Beschreibung
Other abnormalities
Alias
- UMLS CUI-1
- C0522055
- UMLS CUI-2
- C0205394
Ähnliche Modelle
ECG Abnormalities Form Part 2
- StudyEvent: ODM
C0043202 (UMLS CUI [2])
C0024054 (UMLS CUI [3])
C1560305 (UMLS CUI [1,2])
C0947611 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,2])
C0947611 (UMLS CUI [1,3])
C1331539 (UMLS CUI-2)
C0520880 (UMLS CUI-3)
C0438167 (UMLS CUI-4)
C0429059 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,2])
C0947611 (UMLS CUI [1,3])
C0205394 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,2])
C0947611 (UMLS CUI [1,3])
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