ID

23068

Description

Responsible Party: Christoph Bidlingmaier, Consultant Pediatric Hemophilia Center, Ludwig-Maximilians - University of Munich ClinicalTrials.gov Identifier: NCT02912143 History of Changes Other Study ID Numbers: GEPHARD DRKS00011101 ( Registry Identifier: DRKS ) Study First Received: September 17, 2016 Last Updated: January 26, 2017 Individual Participant Data Plan to Share IPD: No Plan Description: Individual Patient data will not be shared outside specified collaborating studies (none yet) German Pediatric Hemophilia Research Database (GEPHARD) ODM derived from:https://clinicaltrials.gov/ct2/show/NCT02912143

Link

https://clinicaltrials.gov/ct2/show/NCT02912143

Keywords

  1. 6/21/17 6/21/17 -
Uploaded on

June 21, 2017

DOI

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License

Creative Commons BY 4.0

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Eligibility Pediatric Hemophilia DRKS00011101 NCT02912143 DRKS00011101

Eligibility Pediatric Hemophilia NCT02912143 DRKS00011101

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI-1
C1512693
Ages Eligible for Study: up to 18 Years (Child, Adult)
Description

Age

Data type

text

Hemophilia A or B
Description

Hemophilia A or B

Data type

boolean

Alias
UMLS CUI [1]
C0019069
UMLS CUI [2]
C0008533
FVIII/FIX <1% to 25%
Description

FVIII/FIX

Data type

boolean

Alias
UMLS CUI [1,1]
C0015506
UMLS CUI [1,2]
C0015491
Informed consent
Description

Informed consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI-1
C0680251
Healthy Volunteers
Description

Control Group

Data type

boolean

Alias
UMLS CUI [1]
C0009932

Similar models

Eligibility Pediatric Hemophilia NCT02912143 DRKS00011101

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Inclusion Criteria
C1512693 (UMLS CUI-1)
Age
Item
Ages Eligible for Study: up to 18 Years (Child, Adult)
text
Hemophilia A or B
Item
Hemophilia A or B
boolean
C0019069 (UMLS CUI [1])
C0008533 (UMLS CUI [2])
FVIII/FIX
Item
FVIII/FIX <1% to 25%
boolean
C0015506 (UMLS CUI [1,1])
C0015491 (UMLS CUI [1,2])
Informed consent
Item
Informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
Exclusion Criteria
C0680251 (UMLS CUI-1)
Control Group
Item
Healthy Volunteers
boolean
C0009932 (UMLS CUI [1])

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