ID
24311
Beschrijving
Study part: Diary Card General Symptoms All groups. A phase 2 study to assess safety, reactogenicity and immunogenicity of a booster dose of an investigational vaccination regimen and GSK Biologicals Hib-MenC vaccine (co-administered with Infanrix penta) compared to a booster dose of Menjugate (co-administered with Infanrix hexa).Patient Level Data: Study Listed on ClinicalStudyDataRequest.com. Study ID: 100381, Clinical Study ID: 100381
Trefwoorden
Versies (1)
- 29-07-17 29-07-17 -
Houder van rechten
GlaxoSmithKline
Geüploaded op
29 juli 2017
DOI
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Licentie
Creative Commons BY-NC 3.0
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Diary Card General Symptoms All groups Hib-MenCY-TT-004 BST 003 Neisseria Meningitidis-Haemophilus influenzae type b Vaccine 100381
Diary Card General Symptoms All groups
- StudyEvent: ODM
Beschrijving
OTHER GENERAL SYMPTOMS
Alias
- UMLS CUI-1
- C1457887
Beschrijving
Description
Datatype
text
Alias
- UMLS CUI [1]
- C0678257
Beschrijving
1:Mild: An adverse event which is easily tolerated by the subject, causing minimal discomfort and not interfering with everyday activities. 2:Moderate: An adverse event which is sufficiently discomforting to interfere with normal everyday activities. 3:Severe: An adverse event which prevents normal, everyday activities. (In a young child, such an adverse event would, for example, prevent attendance at school/kindergarten/a day-care center and would cause the parents/guardians to seek medical advice).
Datatype
text
Alias
- UMLS CUI [1]
- C0518690
Beschrijving
Start date
Datatype
date
Alias
- UMLS CUI [1]
- C0808070
Beschrijving
End date
Datatype
date
Alias
- UMLS CUI [1]
- C0806020
Beschrijving
symptom ongoing
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1457887
- UMLS CUI [1,2]
- C3174772
Beschrijving
Medical advice
Datatype
boolean
Alias
- UMLS CUI [1]
- C1386497
Beschrijving
MEDICATION
Alias
- UMLS CUI-1
- C0013227
Beschrijving
Medication
Datatype
text
Alias
- UMLS CUI [1]
- C0013227
Beschrijving
Reason
Datatype
text
Alias
- UMLS CUI [1]
- C3146298
Beschrijving
Total Daily Dose
Datatype
text
Alias
- UMLS CUI [1]
- C2348070
Beschrijving
Start date
Datatype
date
Alias
- UMLS CUI [1]
- C0808070
Beschrijving
End date
Datatype
date
Alias
- UMLS CUI [1]
- C0806020
Beschrijving
symptom ongoing
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1457887
- UMLS CUI [1,2]
- C3174772
Beschrijving
date
Datatype
date
Alias
- UMLS CUI [1]
- C0011008
Beschrijving
Hospitalization
Datatype
text
Alias
- UMLS CUI [1]
- C0019993
Beschrijving
Telephone number
Datatype
integer
Alias
- UMLS CUI [1]
- C1515258
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- StudyEvent: ODM
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