ID
23862
Description
Study part: Pregnancy Follow- Up Form- Current Pregnancy Information Week 36/ Early Withdrawal Visit.A Phase 2 Multicenter, Double-blind, Placebo-controlled, Study to to Evaluate the Corticosteroid- sparing effects of Mepolizumab in Subjects with Hypereosinophilic Syndromes (HES) and Evaluate Efficacy and Safety of Mepolizumab in Controlling the Clinical Signs and Symptoms of subjects with HES Patient Level Data: Study Listed on ClinicalStudyDataRequest.com. Sponsor: GlaxoSmithKline. Study ID: 100185, Clinical Study ID:MHE100185.
Mots-clés
Versions (1)
- 15/07/2017 15/07/2017 -
Détendeur de droits
GlaxoSmithKline
Téléchargé le
15 juillet 2017
DOI
Pour une demande vous connecter.
Licence
Creative Commons BY-NC 3.0
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Pregnancy Follow- Up Form- Current Pregnancy Information Week 36 Mepolizumab HES NCT00086658
Pregnancy Follow- Up Form- Current Pregnancy Information Week 36
- StudyEvent: ODM
Description
INFANT INFORMATION
Alias
- UMLS CUI-1
- C3840300
Description
Date of birth
Type de données
date
Alias
- UMLS CUI [1,1]
- C0421451
- UMLS CUI [1,2]
- C0000814
Description
Gestational weeks at birth miscarriage
Type de données
integer
Unités de mesure
- Weeks
Alias
- UMLS CUI [1,1]
- C2011191
- UMLS CUI [1,2]
- C0000814
Description
sex
Type de données
text
Alias
- UMLS CUI [1]
- C0079399
Description
Length
Type de données
float
Unités de mesure
- cm
Alias
- UMLS CUI [1]
- C1444754
Description
Weight
Type de données
float
Unités de mesure
- g
Alias
- UMLS CUI [1]
- C0005910
Description
Apgar score
Type de données
integer
Alias
- UMLS CUI [1]
- C0003533
Description
Apgar score
Type de données
integer
Alias
- UMLS CUI [1]
- C0003533
Description
PREGNANCY INFORMATION
Alias
- UMLS CUI-1
- C0032961
Description
DRUG EXPOSURES DURING PREGNANCY
Alias
- UMLS CUI-1
- C0743284
- UMLS CUI-2
- C0032961
Description
Drug Name
Type de données
text
Alias
- UMLS CUI [1]
- C0013227
Description
Route
Type de données
text
Alias
- UMLS CUI [1]
- C0013153
Description
Total Daily Dose
Type de données
text
Alias
- UMLS CUI [1]
- C2348070
Description
Units
Type de données
text
Alias
- UMLS CUI [1]
- C1519795
Description
Started Pre-Study
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0013227
- UMLS CUI [1,2]
- C0451613
Description
Start Date
Type de données
date
Alias
- UMLS CUI [1]
- C0808070
Description
Stop Date
Type de données
date
Alias
- UMLS CUI [1]
- C0806020
Description
Ongoing Medication
Type de données
boolean
Alias
- UMLS CUI [1]
- C2826666
Description
Reason for Medication
Type de données
text
Alias
- UMLS CUI [1,1]
- C0392360
- UMLS CUI [1,2]
- C0013227
Description
REPORTING INVESTIGATOR INFORMATION
Alias
- UMLS CUI-1
- C1955348
- UMLS CUI-2
- C0008961
Description
Name
Type de données
text
Alias
- UMLS CUI [1]
- C0008961
Description
Title
Type de données
text
Alias
- UMLS CUI [1]
- C3888414
Description
Speciality
Type de données
text
Alias
- UMLS CUI [1,1]
- C0037778
- UMLS CUI [1,2]
- C0008961
Description
Address
Type de données
text
Alias
- UMLS CUI [1]
- C1442065
Description
City
Type de données
text
Alias
- UMLS CUI [1]
- C0008848
Description
Country
Type de données
text
Alias
- UMLS CUI [1]
- C0454664
Description
Zip Code
Type de données
integer
Alias
- UMLS CUI [1]
- C0421454
Description
Telephone No
Type de données
integer
Alias
- UMLS CUI [1]
- C1515258
Description
Fax No
Type de données
integer
Alias
- UMLS CUI [1]
- C1549619
Description
Investigator signature
Type de données
text
Alias
- UMLS CUI [1]
- C2346576
Description
Investigator name
Type de données
text
Alias
- UMLS CUI [1]
- C2826892
Description
Date
Type de données
date
Alias
- UMLS CUI [1]
- C0011008
Similar models
Pregnancy Follow- Up Form- Current Pregnancy Information Week 36
- StudyEvent: ODM
C0019994 (UMLS CUI [1,2])
C0034656 (UMLS CUI [1,2])
C0000814 (UMLS CUI [1,2])
C0000814 (UMLS CUI [1,2])
C0022864 (UMLS CUI [1,2])
C0011209 (UMLS CUI [1,3])
C0030685 (UMLS CUI [1,4])
C0032961 (UMLS CUI-2)
C0451613 (UMLS CUI [1,2])
C0013227 (UMLS CUI [1,2])
C0008961 (UMLS CUI-2)
C0008961 (UMLS CUI [1,2])