ID

34464

Description

Randomized Study of Spinal Anesthesia Compared With Traditional Epidural Anesthesia Concerning Peroperative and Postoperative Pain After Open Nephrectomy in Patients With Renal Cell Carcinoma; ODM derived from: https://clinicaltrials.gov/show/NCT02030717

Link

https://clinicaltrials.gov/show/NCT02030717

Keywords

  1. 1/17/19 1/17/19 -
Copyright Holder

see on clinicaltrials.gov

Uploaded on

January 17, 2019

DOI

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License

Creative Commons BY 4.0

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Eligibility Pre- and Postoperative Analgesia NCT02030717

Eligibility Pre- and Postoperative Analgesia NCT02030717

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
all patients in asa score i - iii, planned to be treated with open radical nephrectomy or nephron-sparing surgery having renal cell carcinoma
Description

ID.1

Data type

boolean

Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients in asa score iv-v,
Description

ID.2

Data type

boolean

patients with advanced tumour thrombus in vena cava inferior,
Description

ID.3

Data type

boolean

patients with high risk for bleeding
Description

ID.4

Data type

boolean

patients with previous chronic pain symptoms
Description

ID.5

Data type

boolean

patients having drug abuse
Description

ID.6

Data type

boolean

patients having cognitive deficiencies or dementia disease
Description

ID.7

Data type

boolean

patients with any contraindication of either spinal or epidural anesthesia
Description

ID.8

Data type

boolean

patients younger than 18 years and pregnant woman
Description

ID.9

Data type

boolean

patients having a weight less than 45 kg or weight over 120 kg
Description

ID.10

Data type

boolean

Similar models

Eligibility Pre- and Postoperative Analgesia NCT02030717

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
all patients in asa score i - iii, planned to be treated with open radical nephrectomy or nephron-sparing surgery having renal cell carcinoma
boolean
Item Group
C0680251 (UMLS CUI)
ID.2
Item
patients in asa score iv-v,
boolean
ID.3
Item
patients with advanced tumour thrombus in vena cava inferior,
boolean
ID.4
Item
patients with high risk for bleeding
boolean
ID.5
Item
patients with previous chronic pain symptoms
boolean
ID.6
Item
patients having drug abuse
boolean
ID.7
Item
patients having cognitive deficiencies or dementia disease
boolean
ID.8
Item
patients with any contraindication of either spinal or epidural anesthesia
boolean
ID.9
Item
patients younger than 18 years and pregnant woman
boolean
ID.10
Item
patients having a weight less than 45 kg or weight over 120 kg
boolean

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