ID

13272

Description

Study part: Documentation concomitant medication. Effectiveness and tolerance of sublingual desensitization with LAIS grass tablets in Patients with an allergic rhinoconjunctivitis caused by grass pollen. A prospective, multi-center, doubleblind, randomized, placebo-controlled Phase III study. Principal Investigator Prof. Dr. med. Ralph Mösges.

Keywords

  1. 1/28/16 1/28/16 -
  2. 10/30/19 10/30/19 - Sarah Riepenhausen
Uploaded on

January 28, 2016

DOI

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License

Creative Commons BY-NC 3.0

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Concomitant medication_LAIS grass tablets by allergic rhinoconjunctivitis_EudraCT-Nr.2012-004916-79

Documentation concomitant medication

Concomitant medication
Description

Concomitant medication

Alias
UMLS CUI-1
C2347852
Name of concomitant medication
Description

Concomitant medication

Data type

text

Alias
UMLS CUI [1]
C2347852
Active substance
Description

active substance

Data type

text

Alias
UMLS CUI [1]
C0574031
Medication dose
Description

medication dose

Data type

text

Alias
UMLS CUI [1]
C3174092
Indication of medication
Description

indication medication

Data type

text

Alias
UMLS CUI [1,1]
C3146298
UMLS CUI [1,2]
C0013227
Contraindicated drugs
Description

Antihistamines (including Ketotifen), decongestants (oral/ nasal sprays and drops), Mast cell stabilizers (e.g. Cromoglykate), systemic corticosteroids, topical eye medication, other asthma treatment as inhalable beta-2 agonists and inhaled corticosteroids, antileukotriene, tranquilizers or psychoactive drugs, Anti-IgE antibodies

Data type

boolean

Alias
UMLS CUI [1,1]
C0522473
UMLS CUI [1,2]
C0013227
Medication intake began on
Description

date

Data type

date

Alias
UMLS CUI [1]
C0011008
Medication intake ended on
Description

date

Data type

date

Alias
UMLS CUI [1]
C0011008

Similar models

Documentation concomitant medication

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Concomitant medication
C2347852 (UMLS CUI-1)
Concomitant medication
Item
Name of concomitant medication
text
C2347852 (UMLS CUI [1])
active substance
Item
Active substance
text
C0574031 (UMLS CUI [1])
Item
Medication dose
text
C3174092 (UMLS CUI [1])
Code List
Medication dose
CL Item
daily (1)
CL Item
if necessary (2)
indication medication
Item
Indication of medication
text
C3146298 (UMLS CUI [1,1])
C0013227 (UMLS CUI [1,2])
Contraindicated drugs
Item
Contraindicated drugs
boolean
C0522473 (UMLS CUI [1,1])
C0013227 (UMLS CUI [1,2])
date
Item
Medication intake began on
date
C0011008 (UMLS CUI [1])
date
Item
Medication intake ended on
date
C0011008 (UMLS CUI [1])

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