ID
24311
Descripción
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
Palabras clave
Versiones (1)
- 29/7/17 29/7/17 -
Titular de derechos de autor
GlaxoSmithKline
Subido en
29 de julio de 2017
DOI
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Licencia
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
Descripción
OTHER GENERAL SYMPTOMS
Alias
- UMLS CUI-1
- C1457887
Descripción
Description
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0678257
Descripción
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).
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0518690
Descripción
Start date
Tipo de datos
date
Alias
- UMLS CUI [1]
- C0808070
Descripción
End date
Tipo de datos
date
Alias
- UMLS CUI [1]
- C0806020
Descripción
symptom ongoing
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C1457887
- UMLS CUI [1,2]
- C3174772
Descripción
Medical advice
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C1386497
Descripción
MEDICATION
Alias
- UMLS CUI-1
- C0013227
Descripción
Medication
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0013227
Descripción
Reason
Tipo de datos
text
Alias
- UMLS CUI [1]
- C3146298
Descripción
Total Daily Dose
Tipo de datos
text
Alias
- UMLS CUI [1]
- C2348070
Descripción
Start date
Tipo de datos
date
Alias
- UMLS CUI [1]
- C0808070
Descripción
End date
Tipo de datos
date
Alias
- UMLS CUI [1]
- C0806020
Descripción
symptom ongoing
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C1457887
- UMLS CUI [1,2]
- C3174772
Descripción
date
Tipo de datos
date
Alias
- UMLS CUI [1]
- C0011008
Descripción
Hospitalization
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0019993
Descripción
Telephone number
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C1515258
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- StudyEvent: ODM
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