ID
42510
Descrizione
Study ID: 106464 Clinical Study ID: 106464 Study Title: A Study of the Efficacy Against Episodes of Clinical Malaria Due to P. Falciparum Infection of GSK Biologicals Candidate Vaccine RTS, S/AS01, Administered According to a 0,1,2-months Schedule in Children Aged 5 to 17 Months Living in Tanzania & Kenya Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00380393 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 2 Study Recruitment Status: Completed Generic Name: GSK malaria vaccine 257049 Vaccine, Sanofi-Pasteur's Human Diploid Cell Rabies Vaccine Trade Name: N/A Study Indication: Malaria ODM derived from https://clinicaltrials.gov/ct2/show/study/NCT00380393. This Phase IIb randomized, double-blind, controlled study of the efficacy against episodes of clinical malaria due to Plasmodium falciparum infection of GlaxoSmithKline Biologicals’ candidate vaccine RTS, S/AS01E, administered IM according to a 0, 1, 2-month vaccination schedule in children aged 5 months to 17 months living in Tanzania and Kenya. This study includes the following 7 clinical study visits (3 different visit types) during a double-blind phase (Day -60 to Month 6 1/2) and a single-blind phase including an extension for a subset of patients (month 7 to month 14). Clinical visit 1: Baseline visit, screening, and randomisation (DAY -60 to 0) Clinical visit 2: Vaccination I (MONTH 0, DAY 0 | DOSE 1 | 0 - 60 DAYS AFTER VISIT 1) Clinical visit 3: Vaccination II (MONTH 1, DAY 30 | DOSE 2 | 21 - 35 DAYS AFTER VISIT 2) Clinical visit 4: Vaccination III (MONTH 2, DAY 60 | DOSE 3 | 21 - 35 DAYS AFTER VISIT 3) Clinical visit 5: Blood Sample, ACD (MONTH 3, DAY 90 | 21 - 42 DAYS AFTER VISIT 4) Clinical visit 6: Blood Sample, ACD (MONTH 6 1/2 | CROSS-SECTIONAL VISIT FOR ACD | FINAL STUDY VISIT FOR DOUBLE-BLIND PHASE) Clinical visit 7: Blood Sample, ACD (MONTH 14 | FINAL STUDY VISIT SINGLE-BLIND PHASE) Field-worker home visits: During the vaccination period, clinical visits are accompanied by daily field-worker visits for a one-week period subsequent to each vaccine administration at clinical visits 2, 3, and 4 (visit code 21-26 following clinical visit 2; visit code 27-32 following clinical visit 3; visit code 33-38 following clinical visit 4). After completion of the vaccination period, clinical visits are then accompanied by weekly field-worker home visits (visit code 39-40 following clinical visit 4/dose 3; visit code 41-55 following clinical visit 5; visit code 56-86 following clinical visit 6). These visits serve the additional purpose of Active Case Detection (ACD). Passive Case Detection (PCD) for clinical malaria disease is performed both during the course of the double-blind (day -60 to month 6 1/2) and the single-blind phase (month 7 to month 14). This form should be filled in at every field-worker home visit as well as at clinical visit 5, 6, and 7. For field-worker home visits No° 55 and No° 86, please complete the additional questions as indicated in the form. Note that informed consent has to be obtained prior to any study procedure.
collegamento
https://clinicaltrials.gov/ct2/show/study/NCT00380393
Keywords
versioni (2)
- 01/08/21 01/08/21 -
- 10/08/21 10/08/21 -
Titolare del copyright
GlaxoSmithKline
Caricato su
10 agosto 2021
DOI
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Licenza
Creative Commons BY-NC 4.0
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Efficacy of P. Falciparum Vaccine Against Malaria in Children NCT00380393
Active Case Detection
- StudyEvent: ODM
Descrizione
Active Case Detection for Clinical Malaria Disease
Alias
- UMLS CUI-1
- C0024530
- UMLS CUI-2
- C4290001
Descrizione
Fever ≥ 37.5°C
Tipo di dati
float
Unità di misura
- °C
Alias
- UMLS CUI [1]
- C1531924
Descrizione
Malaria rapid diagnostic test performed
Tipo di dati
boolean
Alias
- UMLS CUI [1,1]
- C5400270
- UMLS CUI [1,2]
- C0884358
Descrizione
Malaria rapid diagnostic test results
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C5400270
- UMLS CUI [1,2]
- C1274040
Descrizione
Malarial parasite detection test density performed
Tipo di dati
boolean
Alias
- UMLS CUI [1,1]
- C1443557
- UMLS CUI [1,2]
- C0178587
- UMLS CUI [1,3]
- C0884358
Descrizione
Malarial parasite detection test density results
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C1443557
- UMLS CUI [1,2]
- C0178587
- UMLS CUI [1,3]
- C1274040
Descrizione
Malarial parasite detection test density unavailability reason
Tipo di dati
text
Alias
- UMLS CUI [1,1]
- C1443557
- UMLS CUI [1,2]
- C0178587
- UMLS CUI [1,3]
- C0686905
- UMLS CUI [1,4]
- C0566251
Descrizione
Malarial parasite detection test density results
Tipo di dati
integer
Unità di misura
- /µL
Alias
- UMLS CUI [1,1]
- C1443557
- UMLS CUI [1,2]
- C0178587
- UMLS CUI [1,3]
- C1274040
Descrizione
Blood sample taken malarial parasite genotyping
Tipo di dati
boolean
Alias
- UMLS CUI [1,1]
- C1277698
- UMLS CUI [1,2]
- C0024530
- UMLS CUI [1,3]
- C0030498
- UMLS CUI [1,4]
- C1285573
Descrizione
Treated Bed Net (only to be completed for field-worker visits No° 55 and No° 86)
Alias
- UMLS CUI-1
- C2717999
Descrizione
Indoor Residual Spray (only to be completed for field-worker visits No° 55 and No° 86)
Alias
- UMLS CUI-1
- C0562498
- UMLS CUI-2
- C2003858
- UMLS CUI-3
- C1609982
- UMLS CUI-4
- C0021576
Descrizione
Indoor residual spray during clinical trial period
Tipo di dati
boolean
Alias
- UMLS CUI [1,1]
- C0562498
- UMLS CUI [1,2]
- C2003858
- UMLS CUI [1,3]
- C1609982
- UMLS CUI [1,4]
- C0021576
- UMLS CUI [1,5]
- C0347984
- UMLS CUI [1,6]
- C2347804
Descrizione
Indoor residual spray start date
Tipo di dati
date
Alias
- UMLS CUI [1,1]
- C0562498
- UMLS CUI [1,2]
- C2003858
- UMLS CUI [1,3]
- C1609982
- UMLS CUI [1,4]
- C0021576
- UMLS CUI [1,5]
- C0808070
Similar models
Active Case Detection
- StudyEvent: ODM
C4290001 (UMLS CUI-2)
C0884358 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,2])
C0178587 (UMLS CUI [1,2])
C0884358 (UMLS CUI [1,3])
C0178587 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C0178587 (UMLS CUI [1,2])
C0686905 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
C0178587 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C0024530 (UMLS CUI [1,2])
C0030498 (UMLS CUI [1,3])
C1285573 (UMLS CUI [1,4])
C2003858 (UMLS CUI-2)
C1609982 (UMLS CUI-3)
C0021576 (UMLS CUI-4)
C2003858 (UMLS CUI [1,2])
C1609982 (UMLS CUI [1,3])
C0021576 (UMLS CUI [1,4])
C0347984 (UMLS CUI [1,5])
C2347804 (UMLS CUI [1,6])
C2003858 (UMLS CUI [1,2])
C1609982 (UMLS CUI [1,3])
C0021576 (UMLS CUI [1,4])
C0808070 (UMLS CUI [1,5])