ID

31033

Descripción

Influence of Diabetes on Tramadol Pharmacokinetics; ODM derived from: https://clinicaltrials.gov/show/NCT02246712

Link

https://clinicaltrials.gov/show/NCT02246712

Palabras clave

Versiones (1)
  1. 12/7/18 12/7/18 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

12 de julio de 2018

DOI

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Licencia

Creative Commons BY 4.0
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Eligibility Neuropathic Pain NCT02246712

Inglés

Eligibility Neuropathic Pain NCT02246712

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
adult patients, both gender
Descripción

Adult

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001675
patients with self-reported neuropathic pain (score >4 in a 0-10 visual analog scale)
Descripción

Neuropathic pain Visual Analog Pain Scale

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C3714625
UMLS CUI [1,2]
C0042815
patients with normal renal function (creatinine clearance >60 ml/min)
Descripción

Renal function | Creatinine clearance measurement

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0232804
UMLS CUI [2]
C0373595
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients with nociceptive somatic pain, visceral or autonomic associated during the study period;
Descripción

Nociceptive Pain Somatic Visceral | Nociceptive Pain Somatic Autonomic

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C3178766
UMLS CUI [1,2]
C2986476
UMLS CUI [1,3]
C0442045
UMLS CUI [2,1]
C3178766
UMLS CUI [2,2]
C2986476
UMLS CUI [2,3]
C0004388
patients with morbid obesity (bmi> 40), congestive heart failure, severe hypertension
Descripción

Obesity, Morbid | Body mass index | Congestive heart failure | Hypertension, severe

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0028756
UMLS CUI [2]
C1305855
UMLS CUI [3]
C0018802
UMLS CUI [4]
C4013784
patients who have had acute myocardial infarction or accident stroke less than 6 months of the period of investigation.
Descripción

Myocardial Infarction | Cerebrovascular accident

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0027051
UMLS CUI [2]
C0038454
patients with chronic obstructive pulmonary disease
Descripción

Chronic Obstructive Airway Disease

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0024117
patients who were in use of analgesics, cyp2d6 inhibitors or cyp3a4 inducers or inhibitors were excluded.
Descripción

Analgesics | CYP2D6 Inhibitors | CYP3A4 Inducer | CYP3A4 Inhibitor

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0002771
UMLS CUI [2]
C3850058
UMLS CUI [3]
C3830625
UMLS CUI [4]
C3830624
pregnant and lactating patients were excluded.
Descripción

Pregnancy | Breast Feeding

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
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Similar models

Eligibility Neuropathic Pain NCT02246712

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Adult
Item
adult patients, both gender
boolean
C0001675 (UMLS CUI [1])
Neuropathic pain Visual Analog Pain Scale
Item
patients with self-reported neuropathic pain (score >4 in a 0-10 visual analog scale)
boolean
C3714625 (UMLS CUI [1,1])
C0042815 (UMLS CUI [1,2])
Renal function | Creatinine clearance measurement
Item
patients with normal renal function (creatinine clearance >60 ml/min)
boolean
C0232804 (UMLS CUI [1])
C0373595 (UMLS CUI [2])
Item Group
C0680251 (UMLS CUI)
Nociceptive Pain Somatic Visceral | Nociceptive Pain Somatic Autonomic
Item
patients with nociceptive somatic pain, visceral or autonomic associated during the study period;
boolean
C3178766 (UMLS CUI [1,1])
C2986476 (UMLS CUI [1,2])
C0442045 (UMLS CUI [1,3])
C3178766 (UMLS CUI [2,1])
C2986476 (UMLS CUI [2,2])
C0004388 (UMLS CUI [2,3])
Obesity, Morbid | Body mass index | Congestive heart failure | Hypertension, severe
Item
patients with morbid obesity (bmi> 40), congestive heart failure, severe hypertension
boolean
C0028756 (UMLS CUI [1])
C1305855 (UMLS CUI [2])
C0018802 (UMLS CUI [3])
C4013784 (UMLS CUI [4])
Myocardial Infarction | Cerebrovascular accident
Item
patients who have had acute myocardial infarction or accident stroke less than 6 months of the period of investigation.
boolean
C0027051 (UMLS CUI [1])
C0038454 (UMLS CUI [2])
Chronic Obstructive Airway Disease
Item
patients with chronic obstructive pulmonary disease
boolean
C0024117 (UMLS CUI [1])
Analgesics | CYP2D6 Inhibitors | CYP3A4 Inducer | CYP3A4 Inhibitor
Item
patients who were in use of analgesics, cyp2d6 inhibitors or cyp3a4 inducers or inhibitors were excluded.
boolean
C0002771 (UMLS CUI [1])
C3850058 (UMLS CUI [2])
C3830625 (UMLS CUI [3])
C3830624 (UMLS CUI [4])
Pregnancy | Breast Feeding
Item
pregnant and lactating patients were excluded.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Volver a la parte superior de la página 

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