Informations:
Erreur:
ID
36550
Description
Decompressive Cervical Surgery and Hypertension; ODM derived from: https://clinicaltrials.gov/show/NCT02016768
Lien
https://clinicaltrials.gov/show/NCT02016768
Mots-clés
Versions (1)
- 21/05/2019 21/05/2019 -
Détendeur de droits
See clinicaltrials.gov
Téléchargé le
21 mai 2019
DOI
Pour une demande vous connecter.
Licence
Creative Commons BY 4.0
Modèle Commentaires :
Ici, vous pouvez faire des commentaires sur le modèle. À partir des bulles de texte, vous pouvez laisser des commentaires spécifiques sur les groupes Item et les Item.
Groupe Item commentaires pour :
Item commentaires pour :
Vous devez être connecté pour pouvoir télécharger des formulaires. Veuillez vous connecter ou s’inscrire gratuitement.
Eligibility Myelopathy, Compressive NCT02016768
Eligibility Myelopathy, Compressive NCT02016768
- StudyEvent: Eligibility
Similar models
Eligibility Myelopathy, Compressive NCT02016768
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Cervical spondylosis with myelopathy
Item
established diagnosis of cervical spondylosis myelopathy
boolean
C0158242 (UMLS CUI [1])
Age
Item
be at least 18 years of age
boolean
C0001779 (UMLS CUI [1])
Systolic Pressure
Item
office-measured systolic bp≧140mmhg
boolean
C0871470 (UMLS CUI [1])
Protocol Compliance
Item
ability to adhere to study protocol
boolean
C0525058 (UMLS CUI [1])
Informed Consent
Item
have signed an approved informed consent form for participation in this study
boolean
C0021430 (UMLS CUI [1])
Hypertensive disease Secondary to Cause | Cause Reversible
Item
have hypertension secondary to a treatable cause
boolean
C0020538 (UMLS CUI [1,1])
C0175668 (UMLS CUI [1,2])
C0015127 (UMLS CUI [1,3])
C0015127 (UMLS CUI [2,1])
C0205343 (UMLS CUI [2,2])
C0175668 (UMLS CUI [1,2])
C0015127 (UMLS CUI [1,3])
C0015127 (UMLS CUI [2,1])
C0205343 (UMLS CUI [2,2])
Cervical spine surgery
Item
have prior cervical spine surgery
boolean
C0742216 (UMLS CUI [1])
Pregnancy | Pregnancy, Planned
Item
are pregnant or contemplating pregnancy during the 3-month follow-up period
boolean
C0032961 (UMLS CUI [1])
C0032992 (UMLS CUI [2])
C0032992 (UMLS CUI [2])
Study Subject Participation Status Denial
Item
people deny to join the study
boolean
C2348568 (UMLS CUI [1,1])
C2700401 (UMLS CUI [1,2])
C2700401 (UMLS CUI [1,2])
Protocol Compliance Unable
Item
are unable to comply with protocol requirements
boolean
C0525058 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,2])
Life Expectancy Limited | Survival Follow-up Unlikely
Item
are unlikely to survive the protocol follow-up period
boolean
C0023671 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0038952 (UMLS CUI [2,1])
C3274571 (UMLS CUI [2,2])
C0750558 (UMLS CUI [2,3])
C0439801 (UMLS CUI [1,2])
C0038952 (UMLS CUI [2,1])
C3274571 (UMLS CUI [2,2])
C0750558 (UMLS CUI [2,3])
Study Subject Participation Status
Item
are enrolled in another concurrent clinical trial
boolean
C2348568 (UMLS CUI [1])
Visual Analog Scale
Item
visual analogue scale≥4
boolean
C3536884 (UMLS CUI [1])