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Pan European Collaboration on Antipsychotic Naive Schizophrenia (PECANS) (PECANS)

Primary Purpose

Schizophrenia

Status
Completed
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
amisulpride
aripiprazole
Sponsored by
University of Copenhagen
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Schizophrenia focused on measuring dopamine, first episode, reward, cognition, MRI, fMRI, PPI, P300, P50 gating, endophenotypes

Eligibility Criteria

18 Years - 45 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

For patients: meeting diagnostic criteria for schizophrenia according to ICD 10 or DSM IV antipsychotic naive The controls will be matched to the patients according to gender age and parental socio-economic status.

-

Exclusion Criteria:

Patients: mental retardation, other chronic diseases, use of antidepressive medicine during the last month,being pregnant, on going substance abuse

Controls: psychiatric diagnosis, psychiatric diagnosis in first-degree relatives,on going drug abuse, mental retardation -

Sites / Locations

  • Center for Neuropsychiatric Schizophrenia Research, University of Copenhagen, Psychiatric Center Glostrup

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

first choice treatment

second choice treatment

Arm Description

Treatment with amisulpride

treatment with aripiprazole

Outcomes

Primary Outcome Measures

Relationship between specific neuropsychiatric measures and improvement on PANSS scores

Secondary Outcome Measures

The relation between D2 binding potential (SPECT) and reward related brain activity (fMRI BOLD response) before and after D2 blockade
Time/dose improvement on PPI and other psychophysiological measures of early information processing after D2 blockade
Disturbances in reward related fMRI BOLD response in antipsychotic naive schizophrenic patients
Structural changes in grey and white matter before and after D2 blockade
Cognitive differences at baseline and changes over time after D2 blockade
The effect of D2 blockade on reward related fMRI BOLD response

Full Information

First Posted
June 21, 2010
Last Updated
May 25, 2016
Sponsor
University of Copenhagen
Collaborators
Glostrup University Hospital, Copenhagen, Rigshospitalet, Denmark, Institute of Psychiatry, London, UMC Utrecht, Copenhagen Hospital Corporation
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1. Study Identification

Unique Protocol Identification Number
NCT01154829
Brief Title
Pan European Collaboration on Antipsychotic Naive Schizophrenia (PECANS)
Acronym
PECANS
Official Title
Pan European Collaboration on Antipsychotic Naive Schizophrenia (PECANS): the Effects of D2 Antagonism on Candidate Endophenotypes
Study Type
Interventional

2. Study Status

Record Verification Date
May 2016
Overall Recruitment Status
Completed
Study Start Date
December 2008 (undefined)
Primary Completion Date
May 2014 (Actual)
Study Completion Date
May 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Copenhagen
Collaborators
Glostrup University Hospital, Copenhagen, Rigshospitalet, Denmark, Institute of Psychiatry, London, UMC Utrecht, Copenhagen Hospital Corporation

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The investigators want to relate disturbances in first-episode schizophrenic patients in (dopaminergic) D2 receptors, brain structure, brain function, and information processing to each other and to psychopathology. Additionally, the investigators want to examine the influence of D2 receptor blockade on these disturbances. The investigators expect disturbances in the dopaminergic system at baseline to correlate with specific structural and functional changes and with disruption in information processing as measured with psychophysiological and neurocognitive methods - and investigators expect D2 receptor blockade to reverse some of the functional and cognitive impairments.
Detailed Description
The study is designed as a 6 week case-control follow-up study of 70 AN FE pt. with SCZ and 70 controls matched with regard to age, gender, and parental socio-economic status. All subjects will be examined with a diagnostic interview (SCAN, Schedule for Clinical Assessment in Neuropsychiatry), medical and family history, and physical examination before inclusion. At baseline all subjects will be examined with single photon emission computed tomography (SPECT), MRI, fMRI, psychophysiology, neurocognition. In addition, they will be screened for drugs, genetic testing, and ECG. Patients will further be examined with clinical validated rating scales to measure psychopathology, subjective well-being, and side-effects. After a period of 6 weeks all assessments are repeated. During that period patients will be treated with amisulpride, while healthy controls will receive no treatment at all. Efficacy of antipsychotic treatment will be evaluated after this initial period of 6 weeks. Based on this evaluation it will be decided to either continue the current (amisulpride) antipsychotic treatment, or to switch to aripiprazole. Efficacy of aripiprazole is evaluated on a monthly basis, if the patient does not respond well enough, than the treatment will be adapted individually. Regardless of treatment, all subjects will be re-assessed in the same test battery as mentioned above, except for SPECT and fMRI, after a period of 6, 12, and 24 months. The developement in specific disturbances and the relationship between these will be analysed.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Schizophrenia
Keywords
dopamine, first episode, reward, cognition, MRI, fMRI, PPI, P300, P50 gating, endophenotypes

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Factorial Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
136 (Actual)

8. Arms, Groups, and Interventions

Arm Title
first choice treatment
Arm Type
Active Comparator
Arm Description
Treatment with amisulpride
Arm Title
second choice treatment
Arm Type
Active Comparator
Arm Description
treatment with aripiprazole
Intervention Type
Drug
Intervention Name(s)
amisulpride
Other Intervention Name(s)
Solian
Intervention Description
Individually dosed, according to symptoms, for a period of 6 weeks
Intervention Type
Drug
Intervention Name(s)
aripiprazole
Other Intervention Name(s)
abilify
Intervention Description
Individually dosed, according to symptoms, for a period of 6 weeks
Primary Outcome Measure Information:
Title
Relationship between specific neuropsychiatric measures and improvement on PANSS scores
Time Frame
6 weeks of medical treatment
Secondary Outcome Measure Information:
Title
The relation between D2 binding potential (SPECT) and reward related brain activity (fMRI BOLD response) before and after D2 blockade
Time Frame
Baseline, 6 weeks
Title
Time/dose improvement on PPI and other psychophysiological measures of early information processing after D2 blockade
Time Frame
Baseline, 2 and 6 weeks, 6,12,24 months
Title
Disturbances in reward related fMRI BOLD response in antipsychotic naive schizophrenic patients
Time Frame
Baseline and 6 weeks follow up
Title
Structural changes in grey and white matter before and after D2 blockade
Time Frame
6 weeks, 6, 12 and 24 months,
Title
Cognitive differences at baseline and changes over time after D2 blockade
Time Frame
Baseline, 6 weeks, 6,12,24 months
Title
The effect of D2 blockade on reward related fMRI BOLD response
Time Frame
6 weeks of medical treatment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: For patients: meeting diagnostic criteria for schizophrenia according to ICD 10 or DSM IV antipsychotic naive The controls will be matched to the patients according to gender age and parental socio-economic status. - Exclusion Criteria: Patients: mental retardation, other chronic diseases, use of antidepressive medicine during the last month,being pregnant, on going substance abuse Controls: psychiatric diagnosis, psychiatric diagnosis in first-degree relatives,on going drug abuse, mental retardation -
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Birte Y Glenthoj, professor
Organizational Affiliation
University of Copenhagen, Psychiatric Center Glostrup, Ndr. Ringvej, DK-2600 Glostrup, Denmark
Official's Role
Study Director
Facility Information:
Facility Name
Center for Neuropsychiatric Schizophrenia Research, University of Copenhagen, Psychiatric Center Glostrup
City
Glostrup
ZIP/Postal Code
DK-2600
Country
Denmark

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
33933719
Citation
Thomas MB, Raghava JM, Pantelis C, Rostrup E, Nielsen MO, Jensen MH, Glenthoj BY, Mandl RCW, Ebdrup BH, Fagerlund B. Associations between cognition and white matter microstructure in first-episode antipsychotic-naive patients with schizophrenia and healthy controls: A multivariate pattern analysis. Cortex. 2021 Jun;139:282-297. doi: 10.1016/j.cortex.2021.03.003. Epub 2021 Mar 18.
Results Reference
derived
PubMed Identifier
30642415
Citation
Wulff S, Nielsen MO, Rostrup E, Svarer C, Jensen LT, Pinborg L, Glenthoj BY. The relation between dopamine D2 receptor blockade and the brain reward system: a longitudinal study of first-episode schizophrenia patients. Psychol Med. 2020 Jan;50(2):220-228. doi: 10.1017/S0033291718004099. Epub 2019 Jan 15.
Results Reference
derived
PubMed Identifier
30560750
Citation
Ebdrup BH, Axelsen MC, Bak N, Fagerlund B, Oranje B, Raghava JM, Nielsen MO, Rostrup E, Hansen LK, Glenthoj BY. Accuracy of diagnostic classification algorithms using cognitive-, electrophysiological-, and neuroanatomical data in antipsychotic-naive schizophrenia patients. Psychol Med. 2019 Dec;49(16):2754-2763. doi: 10.1017/S0033291718003781. Epub 2018 Dec 18.
Results Reference
derived
PubMed Identifier
30420252
Citation
Jessen K, Mandl RCW, Fagerlund B, Bojesen KB, Raghava JM, Obaid HG, Jensen MB, Johansen LB, Nielsen MO, Pantelis C, Rostrup E, Glenthoj BY, Ebdrup BH. Patterns of Cortical Structures and Cognition in Antipsychotic-Naive Patients With First-Episode Schizophrenia: A Partial Least Squares Correlation Analysis. Biol Psychiatry Cogn Neurosci Neuroimaging. 2019 May;4(5):444-453. doi: 10.1016/j.bpsc.2018.09.006. Epub 2018 Sep 25.
Results Reference
derived
PubMed Identifier
29734953
Citation
Jessen K, Rostrup E, Mandl RCW, Nielsen MO, Bak N, Fagerlund B, Glenthoj BY, Ebdrup BH. Cortical structures and their clinical correlates in antipsychotic-naive schizophrenia patients before and after 6 weeks of dopamine D2/3 receptor antagonist treatment. Psychol Med. 2019 Apr;49(5):754-763. doi: 10.1017/S0033291718001198. Epub 2018 May 8.
Results Reference
derived
PubMed Identifier
29373756
Citation
Anhoj S, Odegaard Nielsen M, Jensen MH, Ford K, Fagerlund B, Williamson P, Glenthoj B, Rostrup E. Alterations of Intrinsic Connectivity Networks in Antipsychotic-Naive First-Episode Schizophrenia. Schizophr Bull. 2018 Oct 17;44(6):1332-1340. doi: 10.1093/schbul/sbx171.
Results Reference
derived
PubMed Identifier
22868877
Citation
Nielsen MO, Rostrup E, Wulff S, Bak N, Broberg BV, Lublin H, Kapur S, Glenthoj B. Improvement of brain reward abnormalities by antipsychotic monotherapy in schizophrenia. Arch Gen Psychiatry. 2012 Dec;69(12):1195-204. doi: 10.1001/archgenpsychiatry.2012.847.
Results Reference
derived
Links:
URL
http://www.cinsr.dk/
Description
homepage of the research unit
URL
http://www.cnsr.dk/
Description
homepage of the research unit

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Pan European Collaboration on Antipsychotic Naive Schizophrenia (PECANS)

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