ID
34933
Description
Study ID: 107022 Clinical Study ID: 107022 Study Title: A phase IIb, controlled, randomised, multicenter, single blind study to demonstrate the Non-Inferiority of the low dose influenza vaccine with or without adjuvant AS03 compared with Fluarix (GlaxoSmithKline Biologicals) administered intramuscularly in elderly >= 60 years Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00321373 Study Link: https://clinicaltrials.gov/ct2/show/NCT00321373 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 2 Study Recruitment Status: Completed Generic Name: Candidate Influenza Vaccine GSK1247446A - 2 different formulations Trade Name: FluarixTM Study Indication: Influenza The purpose of his form is to document if the subject has had any adverse events in the course of the study. It should be filled out at the date of vaccination. Visit 1: Day 0, Pre vaccination Visit 2: Day 21, Post vaccination 1 Phone contact: Day 30, post vaccination 1 Visit 3: Day 180, post vaccination 1
Lien
https://clinicaltrials.gov/ct2/show/NCT00321373
Mots-clés
Versions (6)
- 04/02/2019 04/02/2019 -
- 07/02/2019 07/02/2019 -
- 10/02/2019 10/02/2019 -
- 12/02/2019 12/02/2019 -
- 16/02/2019 16/02/2019 -
- 20/02/2019 20/02/2019 - Sarah Riepenhausen
Détendeur de droits
GlaxoSmithKline
Téléchargé le
4 février 2019
DOI
Pour une demande vous connecter.
Licence
Creative Commons BY-NC 3.0
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Demonstration of the Non-Inferiority of the Low Dose Influenza Vaccine Compared with Fluarix NCT00321373
Solicited Adverse Events
- StudyEvent: ODM
Description
Solicited Adverse Events
Alias
- UMLS CUI-1
- C1457887
- UMLS CUI-2
- C0042196
- UMLS CUI-3
- C0877248
Description
If any of these adverse events meets the protocol definition of serious, please complete a Serious Adverse Event report and fax to GSK Biologicals Study Contact for SAE reporting within 24 hours. If "yes" is ticked, please tick No/Yes for each symptom. If Yes is ticked, please complete all items.
Type de données
text
Alias
- UMLS CUI [1,1]
- C1457887
- UMLS CUI [1,2]
- C0042196
- UMLS CUI [1,3]
- C0877248
Description
Solicited Adverse Events Record - Local Symptoms
Alias
- UMLS CUI-1
- C1457887
- UMLS CUI-2
- C0205276
- UMLS CUI-3
- C0042196
Description
If redness, swelling or ecchymosis is ticked, provide size in mm. If pain is ticked, provide intensity from 0-3.
Type de données
text
Alias
- UMLS CUI [1,1]
- C1457887
- UMLS CUI [1,2]
- C0205276
Description
Provide size/intensity of pain
Type de données
integer
Alias
- UMLS CUI [1]
- C0456389
- UMLS CUI [2,1]
- C0030193
- UMLS CUI [2,2]
- C0522510
- UMLS CUI [3]
- C2826182
Description
Provide size/intensity of pain
Type de données
integer
Alias
- UMLS CUI [1]
- C0456389
- UMLS CUI [2,1]
- C0030193
- UMLS CUI [2,2]
- C0522510
- UMLS CUI [3]
- C2826182
Description
Provide size/intensity of pain
Type de données
integer
Alias
- UMLS CUI [1]
- C0456389
- UMLS CUI [2,1]
- C0030193
- UMLS CUI [2,2]
- C0522510
- UMLS CUI [3]
- C2826182
Description
Provide size/intensity of pain
Type de données
integer
Alias
- UMLS CUI [1]
- C0456389
- UMLS CUI [2,1]
- C0030193
- UMLS CUI [2,2]
- C0522510
- UMLS CUI [3]
- C2826182
Description
Provide size/intensity of pain
Type de données
integer
Alias
- UMLS CUI [1]
- C0456389
- UMLS CUI [2,1]
- C0030193
- UMLS CUI [2,2]
- C0522510
- UMLS CUI [3]
- C2826182
Description
Provide size/intensity of pain
Type de données
integer
Alias
- UMLS CUI [1]
- C0456389
- UMLS CUI [2,1]
- C0030193
- UMLS CUI [2,2]
- C0522510
- UMLS CUI [3]
- C2826182
Description
Provide size/intensity of pain
Type de données
integer
Alias
- UMLS CUI [1]
- C0456389
- UMLS CUI [2,1]
- C0030193
- UMLS CUI [2,2]
- C0522510
- UMLS CUI [3]
- C2826182
Description
Ongoing Symptom
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C1457887
- UMLS CUI [1,2]
- C3174772
Description
Date of Last Day of Symptoms
Type de données
date
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C1517741
- UMLS CUI [1,3]
- C1457887
Description
Solicited Adverse Events - General Symptoms
Alias
- UMLS CUI-1
- C0159028
- UMLS CUI-2
- C0042196
- UMLS CUI-3
- C0877248
Description
Solicited Adverse Events Record - General Symptoms
Alias
- UMLS CUI-1
- C0159028
- UMLS CUI-2
- C0042196
- UMLS CUI-3
- C0877248
Description
If any of these adverse events meets the protocol definition of serious, please complete a Serious Adverse Event report and fax to GSK Biologicals Study Contact for SAE reporting within 24 hours. arthralgia = joint pain
Type de données
text
Alias
- UMLS CUI [1]
- C0159028
Description
Provide intensity of fatigue, headache, musle ach, shivering or arthralgia
Type de données
integer
Alias
- UMLS CUI [1,1]
- C0518690
- UMLS CUI [1,2]
- C2826182
Description
Provide intensity of fatigue, headache, musle ach, shivering or arthralgia
Type de données
integer
Alias
- UMLS CUI [1,1]
- C0518690
- UMLS CUI [1,2]
- C2826182
Description
Provide intensity of fatigue, headache, musle ach, shivering or arthralgia
Type de données
integer
Alias
- UMLS CUI [1,1]
- C0518690
- UMLS CUI [1,2]
- C2826182
Description
Provide intensity of fatigue, headache, musle ach, shivering or arthralgia
Type de données
integer
Alias
- UMLS CUI [1,1]
- C0518690
- UMLS CUI [1,2]
- C2826182
Description
Provide intensity of fatigue, headache, musle ach, shivering or arthralgia
Type de données
integer
Alias
- UMLS CUI [1,1]
- C0518690
- UMLS CUI [1,2]
- C2826182
Description
Provide intensity of fatigue, headache, musle ach, shivering or arthralgia
Type de données
integer
Alias
- UMLS CUI [1,1]
- C0518690
- UMLS CUI [1,2]
- C2826182
Description
Provide intensity of fatigue, headache, musle ach, shivering or arthralgia
Type de données
integer
Alias
- UMLS CUI [1,1]
- C0518690
- UMLS CUI [1,2]
- C2826182
Description
Ongoing Symptom
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C1457887
- UMLS CUI [1,2]
- C3174772
Description
Date of Last Day of Symptoms
Type de données
date
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C1517741
- UMLS CUI [1,3]
- C1457887
Description
Causality
Type de données
boolean
Alias
- UMLS CUI [1]
- C0015127
Description
Solicited Adverse Events - Fever
Description
Fever
Type de données
boolean
Alias
- UMLS CUI [1]
- C0015967
Description
If fever is ticked
Type de données
text
Alias
- UMLS CUI [1,1]
- C0449687
- UMLS CUI [1,2]
- C0015967
Description
Provide intensity of fatigue, headache, musle ach, shivering or arthralgia
Type de données
integer
Alias
- UMLS CUI [1,1]
- C0518690
- UMLS CUI [1,2]
- C2826182
Description
Provide intensity of fatigue, headache, musle ach, shivering or arthralgia
Type de données
integer
Alias
- UMLS CUI [1,1]
- C0518690
- UMLS CUI [1,2]
- C2826182
Description
Provide intensity of fatigue, headache, musle ach, shivering or arthralgia
Type de données
integer
Alias
- UMLS CUI [1,1]
- C0518690
- UMLS CUI [1,2]
- C2826182
Description
Provide intensity of fatigue, headache, musle ach, shivering or arthralgia
Type de données
integer
Alias
- UMLS CUI [1,1]
- C0518690
- UMLS CUI [1,2]
- C2826182
Description
Provide intensity of fatigue, headache, musle ach, shivering or arthralgia
Type de données
integer
Alias
- UMLS CUI [1,1]
- C0518690
- UMLS CUI [1,2]
- C2826182
Description
Provide intensity of fatigue, headache, musle ach, shivering or arthralgia
Type de données
integer
Alias
- UMLS CUI [1,1]
- C0518690
- UMLS CUI [1,2]
- C2826182
Description
Provide intensity of fatigue, headache, musle ach, shivering or arthralgia
Type de données
integer
Alias
- UMLS CUI [1,1]
- C0518690
- UMLS CUI [1,2]
- C2826182
Description
Ongoing Symptom
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C1457887
- UMLS CUI [1,2]
- C3174772
Description
Date of Last Day of Symptoms
Type de données
date
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C1517741
- UMLS CUI [1,3]
- C1457887
Description
Causality
Type de données
boolean
Alias
- UMLS CUI [1]
- C0015127
Description
Unsolicited Adverse Events
Alias
- UMLS CUI-1
- C0877248
- UMLS CUI-2
- C0042196
Similar models
Solicited Adverse Events
- StudyEvent: ODM
C0042196 (UMLS CUI-2)
C0877248 (UMLS CUI-3)
C0042196 (UMLS CUI [1,2])
C0877248 (UMLS CUI [1,3])
C0205276 (UMLS CUI-2)
C0042196 (UMLS CUI-3)
C0030193 (UMLS CUI [2,1])
C0522510 (UMLS CUI [2,2])
C2826182 (UMLS CUI [3])
C0030193 (UMLS CUI [2,1])
C0522510 (UMLS CUI [2,2])
C2826182 (UMLS CUI [3])
C0030193 (UMLS CUI [2,1])
C0522510 (UMLS CUI [2,2])
C2826182 (UMLS CUI [3])
C0030193 (UMLS CUI [2,1])
C0522510 (UMLS CUI [2,2])
C2826182 (UMLS CUI [3])
C0030193 (UMLS CUI [2,1])
C0522510 (UMLS CUI [2,2])
C2826182 (UMLS CUI [3])
C0030193 (UMLS CUI [2,1])
C0522510 (UMLS CUI [2,2])
C2826182 (UMLS CUI [3])
C0030193 (UMLS CUI [2,1])
C0522510 (UMLS CUI [2,2])
C2826182 (UMLS CUI [3])
C3174772 (UMLS CUI [1,2])
C1517741 (UMLS CUI [1,2])
C1457887 (UMLS CUI [1,3])
C0042196 (UMLS CUI-2)
C0877248 (UMLS CUI-3)
C0042196 (UMLS CUI [1,2])
C0877248 (UMLS CUI [1,3])
C0042196 (UMLS CUI-2)
C0877248 (UMLS CUI-3)
C2826182 (UMLS CUI [1,2])
C2826182 (UMLS CUI [1,2])
C2826182 (UMLS CUI [1,2])
C2826182 (UMLS CUI [1,2])
C2826182 (UMLS CUI [1,2])
C2826182 (UMLS CUI [1,2])
C2826182 (UMLS CUI [1,2])
C3174772 (UMLS CUI [1,2])
C1517741 (UMLS CUI [1,2])
C1457887 (UMLS CUI [1,3])
C0015967 (UMLS CUI [1,2])
C2826182 (UMLS CUI [1,2])
C2826182 (UMLS CUI [1,2])
C2826182 (UMLS CUI [1,2])
C2826182 (UMLS CUI [1,2])
C2826182 (UMLS CUI [1,2])
C2826182 (UMLS CUI [1,2])
C2826182 (UMLS CUI [1,2])
C3174772 (UMLS CUI [1,2])
C1517741 (UMLS CUI [1,2])
C1457887 (UMLS CUI [1,3])
C0042196 (UMLS CUI-2)
C0042196 (UMLS CUI [1,2])