ID

32059

Beschreibung

Study ID: 103992 Clinical Study ID: 103992 Study Title: Evaluate immunogenicity, reactogenicity & safety of 2 doses of GSK Biologicals’ oral live attenuated HRV vaccine (RIX4414 at 106.5 CCID50) when given concomitantly with OPV versus given alone (HRV vaccine dose given 15 days after the OPV dose) in healthy infants in Bangladesh Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00139334 https://clinicaltrials.gov/ct2/show/NCT00139334 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 2 Study Recruitment Status: Completed Generic Name: Rotavirus Vaccine Trade Name: Rotarix Study Indication: Haemophilus influenzae type b; Neisseria Meningitidis This form contains Contraindications to subsequent vaccination. All items need to be checked prior to any vaccination during the study (Visits 1 - 5). Visit 1 -> Timing: Day 0, Age: 6 weeks +/- 1 week Visit 2 -> Timing: Day 30, Age: 10 weeks +/- 1 week Visit 3 -> Timing: Day 45, Age: 12 weeks +/- 1 week Visit 4 -> Timing: Day 60, Age: 14 weeks +/- 1 week Visit 5 -> Timing: Day 75, Age: 16 weeks +/- 1 week

Link

https://clinicaltrials.gov/ct2/show/NCT00139334

Stichworte

Versionen (2)
  1. 16.10.18 16.10.18 - Sarah Riepenhausen
  2. 16.10.18 16.10.18 - Sarah Riepenhausen
Rechteinhaber

GlaxoSmithKline

Hochgeladen am

16. Oktober 2018

DOI

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Lizenz

Creative Commons BY-NC 3.0
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GSK Biologicals' oral HRV vaccine given with OPV in infants NCT00139334

Englisch

Contraindications to subsequent vaccination

1 Formulare  
Contraindications to subsequent Vaccination: GSK Biologicals' HRV vaccine or its placebo
Beschreibung

Contraindications to subsequent Vaccination: GSK Biologicals' HRV vaccine or its placebo

Alias
UMLS CUI-1
C0522473
UMLS CUI-2
C0597418
Hypersensitivity reaction due to the vaccine [A]
Beschreibung

This adverse event (AEs) constitutes an absolute contraindication to further administration of HRV vaccine or placebo; if this AE occurs during the study, the subject must not receive additional doses of vaccine but may continue other study procedures at the discretion of the investigator. The subject must be followed until resolution of the event, as with any AE:

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0597418
IS [B]
Beschreibung

This adverse event (AEs) constitutes an absolute contraindication to further administration of HRV vaccine or placebo; if this AE occurs during the study, the subject must not receive additional doses of vaccine but may continue other study procedures at the discretion of the investigator. The subject must be followed until resolution of the event, as with any AE:

Datentyp

boolean

Alias
UMLS CUI [1]
C0021933
Axillary temperature >= 37.5 °C, rectal temperature >= 38.0 °C [C]
Beschreibung

This AE constitutes a contraindication to administration of HRV vaccine or placebo at that point in time; if this AE occurs at the time scheduled for vaccination, the subject may be vaccinated at a later date, within the time window specified in the protocol, or withdrawn at the discretion of the investigator. The subject must be followed until resolution of the event, as with any AE.

Datentyp

boolean

Alias
UMLS CUI [1]
C1531924
UMLS CUI [2]
C0489749
GE within 7 days preceding the study vaccine administration. [D]
Beschreibung

This AE constitutes a contraindication to administration of HRV vaccine or placebo at that point in time; if this AE occurs at the time scheduled for vaccination, the subject may be vaccinated at a later date, within the time window specified in the protocol, or withdrawn at the discretion of the investigator. The subject must be followed until resolution of the event, as with any AE.

Datentyp

boolean

Alias
UMLS CUI [1]
C0017160
Contraindications to subsequent Vaccination: GSK Biologicals’ OPV
Beschreibung

Contraindications to subsequent Vaccination: GSK Biologicals’ OPV

Alias
UMLS CUI-1
C0522473
UMLS CUI-2
C0032375
Known systemic hypersensitivity to neomycin or to any other component of the vaccine. Contact dermatitis to neomycin is not a contraindication. [E]
Beschreibung

The following adverse event associated with OPV immunisation constitutes an absolute contraindication to further administration of OPV vaccine; if this adverse event occurs during the study, the subject must be withdrawn and must be followed until resolution of the event as with any adverse event:

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0027603
UMLS CUI [2,1]
C0020517
UMLS CUI [2,2]
C0042210
UMLS CUI [2,3]
C1705248
UMLS CUI [3,1]
C0332300
UMLS CUI [3,2]
C0027603
UMLS CUI [3,3]
C0011616
Subjects suffering from primary and secondary immunodeficiencies. However, symptomatic and asymptomatic infection with human immunodeficiency virus does not contraindicate immunisation with OPV. [F]
Beschreibung

The following adverse event associated with OPV immunisation constitutes an absolute contraindication to further administration of OPV vaccine; if this adverse event occurs during the study, the subject must be withdrawn and must be followed until resolution of the event as with any adverse event:

Datentyp

boolean

Alias
UMLS CUI [1]
C0398686
UMLS CUI [2]
C0398795
UMLS CUI [3,1]
C0332300
UMLS CUI [3,2]
C0019693
As with other vaccines, the administration of OPV should be postponed in subjects suffering from acute severe febrile illness, or persistent diarrhoea or vomiting. The presence of a minor infection, however, is not a contra-indication for immunisation. [G]
Beschreibung

Precaution

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0743842
UMLS CUI [1,2]
C0205082
UMLS CUI [2]
C0011991
UMLS CUI [3,1]
C0042963
UMLS CUI [3,2]
C0205322
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Ähnliche Modelle

Contraindications to subsequent vaccination

1 Formulare
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
Contraindications to subsequent Vaccination: GSK Biologicals' HRV vaccine or its placebo
C0522473 (UMLS CUI-1)
C0597418 (UMLS CUI-2)
Hypersensitivity to vaccine
Item
Hypersensitivity reaction due to the vaccine [A]
boolean
C0020517 (UMLS CUI [1,1])
C0597418 (UMLS CUI [1,2])
IS
Item
IS [B]
boolean
C0021933 (UMLS CUI [1])
Axillary temperature >= 37.5 °C, rectal temperature >= 38.0 °C
Item
Axillary temperature >= 37.5 °C, rectal temperature >= 38.0 °C [C]
boolean
C1531924 (UMLS CUI [1])
C0489749 (UMLS CUI [2])
GE < 7 days before vaccine administration
Item
GE within 7 days preceding the study vaccine administration. [D]
boolean
C0017160 (UMLS CUI [1])
Item Group
Contraindications to subsequent Vaccination: GSK Biologicals’ OPV
C0522473 (UMLS CUI-1)
C0032375 (UMLS CUI-2)
hypersensitvity to neomycin or other vaccine component, except Neomycin contact dermatitis
Item
Known systemic hypersensitivity to neomycin or to any other component of the vaccine. Contact dermatitis to neomycin is not a contraindication. [E]
boolean
C0020517 (UMLS CUI [1,1])
C0027603 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C0042210 (UMLS CUI [2,2])
C1705248 (UMLS CUI [2,3])
C0332300 (UMLS CUI [3,1])
C0027603 (UMLS CUI [3,2])
C0011616 (UMLS CUI [3,3])
primary or secondary immunodeficiencies except infection with HIV
Item
Subjects suffering from primary and secondary immunodeficiencies. However, symptomatic and asymptomatic infection with human immunodeficiency virus does not contraindicate immunisation with OPV. [F]
boolean
C0398686 (UMLS CUI [1])
C0398795 (UMLS CUI [2])
C0332300 (UMLS CUI [3,1])
C0019693 (UMLS CUI [3,2])
acute severe febrile illness, persistent diarrhoea, vomiting
Item
As with other vaccines, the administration of OPV should be postponed in subjects suffering from acute severe febrile illness, or persistent diarrhoea or vomiting. The presence of a minor infection, however, is not a contra-indication for immunisation. [G]
boolean
C0743842 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0011991 (UMLS CUI [2])
C0042963 (UMLS CUI [3,1])
C0205322 (UMLS CUI [3,2])
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