ID

13350

Beschreibung

Early iNO for Oxidative Stress, Vascular Tone and Inflammation in Babies With Hypoxic Respiratory Failure; ODM derived from: https://clinicaltrials.gov/show/NCT01891500

Link

https://clinicaltrials.gov/show/NCT01891500

Stichworte

  1. 07.02.16 07.02.16 -
Hochgeladen am

7. Februar 2016

DOI

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Lizenz

Creative Commons BY 4.0

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Eligibility Persistent Fetal Circulation Syndrome NCT01891500

Eligibility Persistent Fetal Circulation Syndrome NCT01891500

Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI-1
C1512693
Gestational age ≥ 35 weeks gestation
Beschreibung

Gestational age

Datentyp

boolean

Alias
UMLS CUI [1]
C0017504
Age ≤ 48 hours
Beschreibung

Age

Datentyp

boolean

Alias
UMLS CUI [1]
C0001779
Diagnosis of hypoxic respiratory failure (hrf)
Beschreibung

Diagnosis of hypoxic respiratory failure (hrf) as defined by a post-ductal sao2 ≤90% in ≥50% oxygen with a peep of ≥ 6cm or an oxygenation index (oi) ≥ 10 but ≤ 15 when mean airway pressure and pao2 are known.

Datentyp

boolean

Alias
UMLS CUI [1]
C3805211
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
Gestational age < 35 weeks gestation.
Beschreibung

Gestational age

Datentyp

boolean

Alias
UMLS CUI [1]
C1512693
Post-natal age > 48 hours.
Beschreibung

Age

Datentyp

boolean

Alias
UMLS CUI [1]
C0001779
Previous treatment with 100% oxygen for more than 4 hours.
Beschreibung

Oxygen

Datentyp

boolean

Alias
UMLS CUI [1]
C0184633
Confirmed congenital diaphragmatic hernia.
Beschreibung

Congenital diaphragmatic hernia

Datentyp

boolean

Alias
UMLS CUI [1]
C0235833
Suspected or confirmed congenital airway or pulmonary anomaly.
Beschreibung

Congenital airway or pulmonary anomaly.

Datentyp

boolean

Alias
UMLS CUI [1]
C4012443
UMLS CUI [2]
C0158644
Suspected or confirmed chromosomal anomaly or genetic aberration, with the exception of patients with trisomy 21 who do not have complex congenital heart disease.
Beschreibung

Chromosomal anomaly or genetic aberration

Datentyp

boolean

Alias
UMLS CUI [1]
C0008626
UMLS CUI [2]
C0008625
Infants with pneumothorax as the primary cause of their hrf.
Beschreibung

Infants with pneumothorax as the primary cause of their hrf.

Datentyp

boolean

Alias
UMLS CUI [1]
C0032326
Infants with confirmed complex congenital heart disease.
Beschreibung

Congenital heart disease

Datentyp

boolean

Alias
UMLS CUI [1]
C0152021

Ähnliche Modelle

Eligibility Persistent Fetal Circulation Syndrome NCT01891500

Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
Inclusion Criteria
C1512693 (UMLS CUI-1)
Gestational age
Item
Gestational age ≥ 35 weeks gestation
boolean
C0017504 (UMLS CUI [1])
Age
Item
Age ≤ 48 hours
boolean
C0001779 (UMLS CUI [1])
Diagnosis of hypoxic respiratory failure
Item
Diagnosis of hypoxic respiratory failure (hrf)
boolean
C3805211 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Gestational age
Item
Gestational age < 35 weeks gestation.
boolean
C1512693 (UMLS CUI [1])
Age
Item
Post-natal age > 48 hours.
boolean
C0001779 (UMLS CUI [1])
Oxygen
Item
Previous treatment with 100% oxygen for more than 4 hours.
boolean
C0184633 (UMLS CUI [1])
Congenital diaphragmatic hernia
Item
Confirmed congenital diaphragmatic hernia.
boolean
C0235833 (UMLS CUI [1])
Congenital airway or pulmonary anomaly.
Item
Suspected or confirmed congenital airway or pulmonary anomaly.
boolean
C4012443 (UMLS CUI [1])
C0158644 (UMLS CUI [2])
Chromosomal anomaly or genetic aberration
Item
Suspected or confirmed chromosomal anomaly or genetic aberration, with the exception of patients with trisomy 21 who do not have complex congenital heart disease.
boolean
C0008626 (UMLS CUI [1])
C0008625 (UMLS CUI [2])
Infants with pneumothorax as the primary cause of their hrf.
Item
Infants with pneumothorax as the primary cause of their hrf.
boolean
C0032326 (UMLS CUI [1])
Congenital heart disease
Item
Infants with confirmed complex congenital heart disease.
boolean
C0152021 (UMLS CUI [1])

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