ID
39857
Descripción
Study ID: 110399 Clinical Study ID: 110399 Study Title: A randomized, double blind, parallel group, placebo controlled 28 day study to investigate the safety, tolerability and pharmacodynamics of SB-656933 in subjects with cystic fibrosis. Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00903201 https://clinicaltrials.gov/ct2/show/NCT00903201?term=NCT00903201 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 2 Study Recruitment Status: Completed Generic Name: SB656933, Placebo Trade Name: N/A Study Indication: Cystic Fibrosis The study consists of a screening, five study visits and a follow-up (time relative to Baseline in days): Visit 1: Screening, Day -28 to -16 Visit 2a: Day -7 to -4 Visit 2b: Day 1 Visit 3: Day 14 Visit 4: Day 21 Visit 5: Day 28 Visit 6: Early Withdrawal/ Follow-up, Day 35 to 42. From day 1 to day 28 the patients will receive daily doses. This document contains the 12-Lead-ECG form. It has to be filled in for screening, V2b, V3, V5, follow-up and if required for logs/ repeats.
Link
https://clinicaltrials.gov/ct2/show/NCT00903201?term=NCT00903201
Palabras clave
Versiones (1)
- 24/2/20 24/2/20 -
Titular de derechos de autor
GlaxoSmithKline
Subido en
24 de febrero de 2020
DOI
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Licencia
Creative Commons BY-NC 4.0
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Safety, tolerability and pharmacodynamics of Elubrixin in cystic fibrosis patients, NCT00903201
12-Lead-ECG
- StudyEvent: ODM
Descripción
12-Lead-ECG
Alias
- UMLS CUI-1
- C0430456
Descripción
Only to fill in for screening. For the visits 2b the measurement has to be pre-dose. Also for V3 and V5 there has to be a pre-dose single measurement.
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0242485
- UMLS CUI [1,2]
- C0237753
Descripción
day month year
Tipo de datos
date
Alias
- UMLS CUI [1]
- C2826640
Descripción
00:00-23:59
Tipo de datos
time
Alias
- UMLS CUI [1,1]
- C0040223
- UMLS CUI [1,2]
- C0013798
Descripción
Heart rate
Tipo de datos
integer
Unidades de medida
- beats/min
Alias
- UMLS CUI [1]
- C0018810
Descripción
PR Interval
Tipo de datos
float
Unidades de medida
- msec
Alias
- UMLS CUI [1]
- C0429087
Descripción
QRS Duration
Tipo de datos
float
Unidades de medida
- msec
Alias
- UMLS CUI [1,1]
- C0430456
- UMLS CUI [1,2]
- C0429025
Descripción
Uncorrected QT Interval
Tipo de datos
float
Unidades de medida
- msec
Alias
- UMLS CUI [1,1]
- C0430456
- UMLS CUI [1,2]
- C1287082
- UMLS CUI [1,3]
- C4072785
Descripción
If machine, please provide the QTCB in the appropriate item. If manual, please provide RR interval in the appropriate item.
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0855331
- UMLS CUI [1,2]
- C2911685
Descripción
QTCB
Tipo de datos
float
Unidades de medida
- msec
Alias
- UMLS CUI [1,1]
- C2911685
- UMLS CUI [1,2]
- C0336779
- UMLS CUI [1,3]
- C1882512
- UMLS CUI [1,4]
- C0855331
Descripción
RR interval
Tipo de datos
float
Unidades de medida
- msec
Alias
- UMLS CUI [1,1]
- C2911685
- UMLS CUI [1,2]
- C0175674
- UMLS CUI [1,3]
- C0489636
- UMLS CUI [1,4]
- C0855331
Descripción
If you tick "Abnormal - Clinically significant", please complete the ECG abnormality form for all clinically significant abnormalities, and additionally complete the AE form if the abnormality meets the protocol definition for an AE
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0430456
- UMLS CUI [1,2]
- C1274040
Similar models
12-Lead-ECG
- StudyEvent: ODM
C0237753 (UMLS CUI [1,2])
C0013798 (UMLS CUI [1,2])
C0429025 (UMLS CUI [1,2])
C1287082 (UMLS CUI [1,2])
C4072785 (UMLS CUI [1,3])
C2911685 (UMLS CUI [1,2])
C0336779 (UMLS CUI [1,2])
C1882512 (UMLS CUI [1,3])
C0855331 (UMLS CUI [1,4])
C0175674 (UMLS CUI [1,2])
C0489636 (UMLS CUI [1,3])
C0855331 (UMLS CUI [1,4])
C1274040 (UMLS CUI [1,2])