ID

32134

Beschrijving

D-serine Monotherapy for Schizophrenia; ODM derived from: https://clinicaltrials.gov/show/NCT00816894

Link

https://clinicaltrials.gov/show/NCT00816894

Trefwoorden

Versies (1)
  1. 20-10-18 20-10-18 -
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See clinicaltrials.gov

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20 oktober 2018

DOI

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Creative Commons BY 4.0
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Eligibility Schizophrenia NCT00816894

Engels

Eligibility Schizophrenia NCT00816894

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
1. age 18-70;
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
2. diagnosis of schizophrenia/schizoaffective disorder according to dsm-iv criteria.
Beschrijving

Schizophrenia | Schizoaffective Disorder

Datatype

boolean

Alias
UMLS CUI [1]
C0036341
UMLS CUI [2]
C0036337
3. stable dose antipsychotic treatment for at least 4 weeks;
Beschrijving

Antipsychotic drug therapy Dose Stable

Datatype

boolean

Alias
UMLS CUI [1,1]
C1319421
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C0205360
4. treatment refractoriness according to kane et al.(1988) criteria.
Beschrijving

Unresponsive to Treatment

Datatype

boolean

Alias
UMLS CUI [1]
C0205269
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
1. meeting criteria for other dsm-iv axis i diagnoses ;
Beschrijving

Axis I diagnosis Other

Datatype

boolean

Alias
UMLS CUI [1,1]
C0270287
UMLS CUI [1,2]
C0205394
2. substance abuse or alcoholism during entire lifetime;
Beschrijving

Substance Use Disorders Lifetime | Chronic Alcoholic Intoxication Lifetime

Datatype

boolean

Alias
UMLS CUI [1,1]
C0038586
UMLS CUI [1,2]
C4071830
UMLS CUI [2,1]
C0001973
UMLS CUI [2,2]
C4071830
3. are judged clinically to be at suicidal or homicidal risk;
Beschrijving

At risk for suicide | At risk Homicide

Datatype

boolean

Alias
UMLS CUI [1]
C0563664
UMLS CUI [2,1]
C1444641
UMLS CUI [2,2]
C0019872
4. female patients who are pregnant or lactating; female patients who are not pregnant or lactating, if sexually active, must be using medically accepted means of contraception;
Beschrijving

Pregnancy | Breast Feeding | Gender Sexually active Contraceptive methods

Datatype

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
UMLS CUI [3,1]
C0079399
UMLS CUI [3,2]
C0241028
UMLS CUI [3,3]
C0700589
5. patients with known intolerance to ola treatment or who have failed an adequate trial of ola (at least 6 weeks) at high doses (20 mg/day or higher);
Beschrijving

Intolerance to Olanzapine | Olanzapine High dose failed

Datatype

boolean

Alias
UMLS CUI [1,1]
C1744706
UMLS CUI [1,2]
C0171023
UMLS CUI [2,1]
C0171023
UMLS CUI [2,2]
C0444956
UMLS CUI [2,3]
C0231175
6. patients treated with depot antipsychotics or ect within the eight weeks prior to study entry.
Beschrijving

Injection of depot antipsychotic agent | Electroconvulsive Therapy

Datatype

boolean

Alias
UMLS CUI [1]
C2585377
UMLS CUI [2]
C0013806
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Similar models

Eligibility Schizophrenia NCT00816894

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
1. age 18-70;
boolean
C0001779 (UMLS CUI [1])
Schizophrenia | Schizoaffective Disorder
Item
2. diagnosis of schizophrenia/schizoaffective disorder according to dsm-iv criteria.
boolean
C0036341 (UMLS CUI [1])
C0036337 (UMLS CUI [2])
Antipsychotic drug therapy Dose Stable
Item
3. stable dose antipsychotic treatment for at least 4 weeks;
boolean
C1319421 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0205360 (UMLS CUI [1,3])
Unresponsive to Treatment
Item
4. treatment refractoriness according to kane et al.(1988) criteria.
boolean
C0205269 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Axis I diagnosis Other
Item
1. meeting criteria for other dsm-iv axis i diagnoses ;
boolean
C0270287 (UMLS CUI [1,1])
C0205394 (UMLS CUI [1,2])
Substance Use Disorders Lifetime | Chronic Alcoholic Intoxication Lifetime
Item
2. substance abuse or alcoholism during entire lifetime;
boolean
C0038586 (UMLS CUI [1,1])
C4071830 (UMLS CUI [1,2])
C0001973 (UMLS CUI [2,1])
C4071830 (UMLS CUI [2,2])
At risk for suicide | At risk Homicide
Item
3. are judged clinically to be at suicidal or homicidal risk;
boolean
C0563664 (UMLS CUI [1])
C1444641 (UMLS CUI [2,1])
C0019872 (UMLS CUI [2,2])
Pregnancy | Breast Feeding | Gender Sexually active Contraceptive methods
Item
4. female patients who are pregnant or lactating; female patients who are not pregnant or lactating, if sexually active, must be using medically accepted means of contraception;
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0079399 (UMLS CUI [3,1])
C0241028 (UMLS CUI [3,2])
C0700589 (UMLS CUI [3,3])
Intolerance to Olanzapine | Olanzapine High dose failed
Item
5. patients with known intolerance to ola treatment or who have failed an adequate trial of ola (at least 6 weeks) at high doses (20 mg/day or higher);
boolean
C1744706 (UMLS CUI [1,1])
C0171023 (UMLS CUI [1,2])
C0171023 (UMLS CUI [2,1])
C0444956 (UMLS CUI [2,2])
C0231175 (UMLS CUI [2,3])
Injection of depot antipsychotic agent | Electroconvulsive Therapy
Item
6. patients treated with depot antipsychotics or ect within the eight weeks prior to study entry.
boolean
C2585377 (UMLS CUI [1])
C0013806 (UMLS CUI [2])
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