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D20.215.894 ×
- Clinical Trial (10)
- Follow-Up Studies (10)
- Hepatitis B Vaccines (5)
- Haemophilus influenzae type b (4)
- Adverse event (3)
- Neisseria meningitidis (3)
- Physical Examination (2)
- Clinical Trial, Phase IV (2)
- Concomitant Medication (2)
- Demography (2)
- Eligibility Determination (2)
- Immunization, Secondary (2)
- Patient Participation (2)
- Clinical Trial, Phase II (1)
- Clinical Trial, Phase III (1)
- Malaria Vaccines (1)
- Body Temperature (1)
- Meningococcal Vaccines (1)
- Diphtheria-Tetanus-acellular Pertussis Vaccines (1)
- Case Reports (1)
- Drug-Related Side Effects and Adverse Reactions (1)
- On-Study Form (1)
- Communicable Diseases (1)
- Hepatitis B (1)
- Laboratories (1)
- Malaria (1)
- Medical History Taking (1)
- Pain (1)
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Groupes Item: Administrative data, Absences of ≥ 2 weeks, Dates of Absence from Study area
Groupes Item: Administrative data, Informed Consent, Demographics, Eligibility Check, Inclusion Criteria, Exclusion Criteria, General Medical History / Physical Examination, Meningococcal Vaccination History, Pertussis Vaccination History, Disease History, Laboratory Tests - Blood, Medication, Study Conclusion, Investigator's Confirmation, Reason for non participation, Investigator's Data, Use of Human Samples by GSK, Investigator's Signature
Study of Long-term Antibody Persistence After a Booster Dose of Menitorix Vaccine - 109664 - Visit 1
Groupes Item: Administrative data, Informed Consent, Demographics, Eligibility Check, Inclusion Criteria, Exclusion Criteria, General Medical History / Physical Examination, Meningococcal Vaccination History, Hib Vaccination History, Pertussis Vaccination History, Disease History, Laboratory Tests - Blood, Medication, Study Conclusion, Investigator's Confirmation
Groupes Item: Administrative data, Report of Physical Examination, Associated signs, If hospitalisation is required, please also complete a Serious Adverse Event Form, Clinical Case Description
Groupes Item: Tracking Document Safety Follow-Up, Administrative documentation
Groupes Item: Serious adverse events, Study vaccine information, Concomitant medication / vaccination, Intercurrent illness & medical history, Drug(s) used to treat SAE, SAE administative information
Groupes Item: Patient Administration, Informed Consent, Demographics, Laboratory tests, Vaccination
Groupes Item: Follow-up studies, Administrative documentation
Groupes Item: Tracking Document Safety Follow-Up, Administrative documentation
Groupe Item: Check for Study Continuation