ID

42565

Beschreibung

Pravastatin for Hyperlipidaemia in HIV.; ODM derived from: https://clinicaltrials.gov/show/NCT00227500

Link

https://clinicaltrials.gov/show/NCT00227500

Stichworte

  1. 23.05.16 23.05.16 -
  2. 02.09.21 02.09.21 -
Hochgeladen am

2. September 2021

DOI

Für eine Beantragung loggen Sie sich ein.

Lizenz

Creative Commons BY 4.0

Modell Kommentare :

Hier können Sie das Modell kommentieren. Über die Sprechblasen an den Itemgruppen und Items können Sie diese spezifisch kommentieren.

Itemgroup Kommentare für :

Item Kommentare für :

Um Formulare herunterzuladen müssen Sie angemeldet sein. Bitte loggen Sie sich ein oder registrieren Sie sich kostenlos.

Eligibility HIV Infections NCT00227500

Eligibility HIV Infections NCT00227500

Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
provide written informed consent to participate in the trial
Beschreibung

written informed consent

Datentyp

boolean

Alias
UMLS CUI [1]
C0021430
hiv-1 sero-positive
Beschreibung

HIV-1 sero-positive

Datentyp

boolean

Alias
UMLS CUI [1]
C0019704
male/female >18 years age
Beschreibung

age

Datentyp

boolean

Alias
UMLS CUI [1]
C0001779
currently receiving hiv protease inhibitor therapy for > 12 weeks and unlikely to require change in existing regimen during the 16 week study period
Beschreibung

receiving hiv protease inhibitor therapy

Datentyp

boolean

Alias
UMLS CUI [1]
C0162714
fasting cholesterol > 6.5 mmol/l (mean of 2 samples collected > 3 days apart)
Beschreibung

fasting cholesterol

Datentyp

boolean

Alias
UMLS CUI [1]
C1282513
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
any condition which may interfere with ability to comply with study
Beschreibung

ability to comply with study

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0009488
UMLS CUI [1,2]
C2348568
UMLS CUI [1,3]
C0439801
gastrointestinal disorder which may affect drug absorption
Beschreibung

gastrointestinal disorder

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0017178
UMLS CUI [1,2]
C0521102
UMLS CUI [1,3]
C0678745
hypertension or congestive cardiac failure
Beschreibung

hypertension or congestive cardiac failure

Datentyp

boolean

Alias
UMLS CUI [1]
C0020538
UMLS CUI [2]
C0018802
lactic acidemia (serum lactate level >2.2 mmol/l)
Beschreibung

lactic acidemia

Datentyp

boolean

Alias
UMLS CUI [1]
C0347959
any serious medical condition which may compromise the patient’s safety, including pancreatitis or hepatitis within past 6 months
Beschreibung

serious medical condition

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0009488
UMLS CUI [1,2]
C1113679
UMLS CUI [1,3]
C0439801
active aids defining conditions
Beschreibung

active aids

Datentyp

boolean

Alias
UMLS CUI [1]
C0001175
concurrent therapy with any other lipid lowering agents, oral hypoglycaemics, anabolic steroids or insulin
Beschreibung

lipid lowering agents oral hypoglycaemics anabolic steroids or insulin

Datentyp

boolean

Alias
UMLS CUI [1]
C0003367
UMLS CUI [2]
C0359086
UMLS CUI [3]
C0002845
UMLS CUI [4]
C0021641

Ähnliche Modelle

Eligibility HIV Infections NCT00227500

Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
written informed consent
Item
provide written informed consent to participate in the trial
boolean
C0021430 (UMLS CUI [1])
HIV-1 sero-positive
Item
hiv-1 sero-positive
boolean
C0019704 (UMLS CUI [1])
age
Item
male/female >18 years age
boolean
C0001779 (UMLS CUI [1])
receiving hiv protease inhibitor therapy
Item
currently receiving hiv protease inhibitor therapy for > 12 weeks and unlikely to require change in existing regimen during the 16 week study period
boolean
C0162714 (UMLS CUI [1])
fasting cholesterol
Item
fasting cholesterol > 6.5 mmol/l (mean of 2 samples collected > 3 days apart)
boolean
C1282513 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
ability to comply with study
Item
any condition which may interfere with ability to comply with study
boolean
C0009488 (UMLS CUI [1,1])
C2348568 (UMLS CUI [1,2])
C0439801 (UMLS CUI [1,3])
gastrointestinal disorder
Item
gastrointestinal disorder which may affect drug absorption
boolean
C0017178 (UMLS CUI [1,1])
C0521102 (UMLS CUI [1,2])
C0678745 (UMLS CUI [1,3])
hypertension or congestive cardiac failure
Item
hypertension or congestive cardiac failure
boolean
C0020538 (UMLS CUI [1])
C0018802 (UMLS CUI [2])
lactic acidemia
Item
lactic acidemia (serum lactate level >2.2 mmol/l)
boolean
C0347959 (UMLS CUI [1])
serious medical condition
Item
any serious medical condition which may compromise the patient’s safety, including pancreatitis or hepatitis within past 6 months
boolean
C0009488 (UMLS CUI [1,1])
C1113679 (UMLS CUI [1,2])
C0439801 (UMLS CUI [1,3])
active aids
Item
active aids defining conditions
boolean
C0001175 (UMLS CUI [1])
lipid lowering agents oral hypoglycaemics anabolic steroids or insulin
Item
concurrent therapy with any other lipid lowering agents, oral hypoglycaemics, anabolic steroids or insulin
boolean
C0003367 (UMLS CUI [1])
C0359086 (UMLS CUI [2])
C0002845 (UMLS CUI [3])
C0021641 (UMLS CUI [4])

Benutzen Sie dieses Formular für Rückmeldungen, Fragen und Verbesserungsvorschläge.

Mit * gekennzeichnete Felder sind notwendig.

Benötigen Sie Hilfe bei der Suche? Um mehr Details zu erfahren und die Suche effektiver nutzen zu können schauen Sie sich doch das entsprechende Video auf unserer Tutorial Seite an.

Zum Video