Engelsk

Eligibility Endstage Renal Disease NCT00745719

1 Formulär  
Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
endstage renal disease patients receiving either long-term hemodialysis or peritoneal dialysis treatment, with elevated intact parathyroid hormone (ipth) levels > 500pg/ml on two or more occasions.
Beskrivning

Kidney Failure, Chronic | Chronic haemodialysis | Peritoneal Dialysis | Intact Parathyroid Hormone Measurement Elevated Quantity

Datatyp

boolean

Alias
UMLS CUI [1]
C0022661
UMLS CUI [2]
C1740835
UMLS CUI [3]
C0031139
UMLS CUI [4,1]
C2697755
UMLS CUI [4,2]
C3163633
UMLS CUI [4,3]
C1265611
patients with parathyroid nodular or diffuse hyperplasia identified by ultrasound imaging or radioisotope scan.
Beskrivning

Parathyroid hyperplasia Nodular Ultrasonography | Diffuse hyperplasia Ultrasonography | Parathyroid hyperplasia Nodular Radionuclide Imaging | Diffuse hyperplasia Radionuclide Imaging

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0271844
UMLS CUI [1,2]
C0205297
UMLS CUI [1,3]
C0041618
UMLS CUI [2,1]
C1265933
UMLS CUI [2,2]
C0041618
UMLS CUI [3,1]
C0271844
UMLS CUI [3,2]
C0205297
UMLS CUI [3,3]
C0034606
UMLS CUI [4,1]
C1265933
UMLS CUI [4,2]
C0034606
patients who provide informed consent for the study.
Beskrivning

Informed Consent

Datatyp

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients with significant background valvular heart disease
Beskrivning

Heart valve disease

Datatyp

boolean

Alias
UMLS CUI [1]
C0018824
patients who are unfit for general anaesthesia
Beskrivning

Patients Unfit General Anesthesia

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0030705
UMLS CUI [1,2]
C3841806
UMLS CUI [1,3]
C0002915
patients with acute myocardial infarction within recent two months
Beskrivning

Myocardial Infarction

Datatyp

boolean

Alias
UMLS CUI [1]
C0027051
patients with poor general condition
Beskrivning

Reduced general condition

Datatyp

boolean

Alias
UMLS CUI [1]
C1112627
patients with plans for living related kidney transplant within 1 year
Beskrivning

Kidney Transplantation Living related Planned

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0022671
UMLS CUI [1,2]
C3841816
UMLS CUI [1,3]
C1301732
patients with previous history of parathyroidectomy
Beskrivning

Parathyroidectomy

Datatyp

boolean

Alias
UMLS CUI [1]
C0079989
patients with calciphylaxis
Beskrivning

Calciphylaxis

Datatyp

boolean

Alias
UMLS CUI [1]
C0006666
patients with underlying active malignancy
Beskrivning

Malignant Neoplasms Etiology

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0006826
UMLS CUI [1,2]
C0015127
patients with contraindication for mri
Beskrivning

Medical contraindication Magnetic Resonance Imaging

Datatyp

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0024485
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Similar models

Eligibility Endstage Renal Disease NCT00745719

1 Formulär
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
Kidney Failure, Chronic | Chronic haemodialysis | Peritoneal Dialysis | Intact Parathyroid Hormone Measurement Elevated Quantity
Item
endstage renal disease patients receiving either long-term hemodialysis or peritoneal dialysis treatment, with elevated intact parathyroid hormone (ipth) levels > 500pg/ml on two or more occasions.
boolean
C0022661 (UMLS CUI [1])
C1740835 (UMLS CUI [2])
C0031139 (UMLS CUI [3])
C2697755 (UMLS CUI [4,1])
C3163633 (UMLS CUI [4,2])
C1265611 (UMLS CUI [4,3])
Parathyroid hyperplasia Nodular Ultrasonography | Diffuse hyperplasia Ultrasonography | Parathyroid hyperplasia Nodular Radionuclide Imaging | Diffuse hyperplasia Radionuclide Imaging
Item
patients with parathyroid nodular or diffuse hyperplasia identified by ultrasound imaging or radioisotope scan.
boolean
C0271844 (UMLS CUI [1,1])
C0205297 (UMLS CUI [1,2])
C0041618 (UMLS CUI [1,3])
C1265933 (UMLS CUI [2,1])
C0041618 (UMLS CUI [2,2])
C0271844 (UMLS CUI [3,1])
C0205297 (UMLS CUI [3,2])
C0034606 (UMLS CUI [3,3])
C1265933 (UMLS CUI [4,1])
C0034606 (UMLS CUI [4,2])
Informed Consent
Item
patients who provide informed consent for the study.
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Heart valve disease
Item
patients with significant background valvular heart disease
boolean
C0018824 (UMLS CUI [1])
Patients Unfit General Anesthesia
Item
patients who are unfit for general anaesthesia
boolean
C0030705 (UMLS CUI [1,1])
C3841806 (UMLS CUI [1,2])
C0002915 (UMLS CUI [1,3])
Myocardial Infarction
Item
patients with acute myocardial infarction within recent two months
boolean
C0027051 (UMLS CUI [1])
Reduced general condition
Item
patients with poor general condition
boolean
C1112627 (UMLS CUI [1])
Kidney Transplantation Living related Planned
Item
patients with plans for living related kidney transplant within 1 year
boolean
C0022671 (UMLS CUI [1,1])
C3841816 (UMLS CUI [1,2])
C1301732 (UMLS CUI [1,3])
Parathyroidectomy
Item
patients with previous history of parathyroidectomy
boolean
C0079989 (UMLS CUI [1])
Calciphylaxis
Item
patients with calciphylaxis
boolean
C0006666 (UMLS CUI [1])
Malignant Neoplasms Etiology
Item
patients with underlying active malignancy
boolean
C0006826 (UMLS CUI [1,1])
C0015127 (UMLS CUI [1,2])
Medical contraindication Magnetic Resonance Imaging
Item
patients with contraindication for mri
boolean
C1301624 (UMLS CUI [1,1])
C0024485 (UMLS CUI [1,2])
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