- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT01786369
Adherence in Patients Admitted to a Psychiatric Unit for Acute Psychosis: an Analysis of Serum Levels of Antipsychotics.
13. april 2015 oppdatert av: Leonardo Lopez, Northwell Health
Determination of Adherence in Patients Admitted to a Psychiatric Unit for Decompensated Psychosis: an Analysis of Serum Levels of Antipsychotics.
This is a screening study aimed at estimating the frequency of antipsychotic non-compliance in patients with a history of schizophrenia or other psychotic disorder admitted to an inpatient psychiatric unit.
Levels of the antipsychotics risperidone, olanzapine, quetiapine, aripiprazole, and paliperidone will be drawn in patients presenting the emergency room who are acutely psychotic, require admission to an inpatient hospital, have a history of psychosis, and have previously been prescribed one of the study drugs.
Levels will then be analyzed to determine the frequency and severity of non-compliance in this population.
Studieoversikt
Status
Fullført
Detaljert beskrivelse
We hypothesize that a majority of patients admitted to an inpatient psychiatric service for an acute exacerbation of schizophrenia, schizoaffective disorder, or bipolar I disorder will have plasma levels of antipsychotic below the lower threshold of the accepted therapeutic range as determined by the Arbeitsgemeinschaft fur Neuropsychopharmakologie und Pharmakopsychiatrie (AGNP).
We aim to estimate the frequency of total and partial non-compliance with antipsychotics in adults with schizophrenia, schizoaffective disorder, or bipolar I disorder who are admitted to an inpatient psychiatric service with psychosis.
In order to do so, we will measure serum levels of five commonly prescribed antipsychotics (risperidone, olanzapine, quetiapine, paliperidone and aripiprazole) drawn in the emergency room setting to establish the degree of compliance in admitted patients.
On admission to the inpatient psychiatry service, blood is routinely drawn on all patients via single venipuncture for review of basic laboratory values; 2 tubes are typically drawn.
Investigators will collect a third tube (approximately 2-3 mLs) on all patients prescribed one of the above medications who are admitted with a psychotic decompensation.
This will continue until 100 patients are enrolled.
The extra blood will be sent for determination of serum level of the drug in question.
Each subject will be assigned a unique identification number generated by the principle investigator, and data will be coded using this number.
The following data: age, gender, ethnicity, body mass index, specific diagnosis, and prescribed dosage of the drug in question will be obtained from the subject's medical records.
We will then use the AGNP expert group consensus guidelines for therapeutic drug monitoring to determine the degree of compliance in the specific patient.
All data will be obtained from information available to the clinician (demographic data and previous dosing) or obtained from the small additional blood sample.
Samples will not be stored for future use; residual samples will be destroyed.
For the purposes of this exploratory pilot study we are primarily interested in determining the proportion of patients receiving any of five antipsychotic drugs who have blood levels below an expected therapeutic range.
100 subjects will permit an initial estimate with reasonable confidence intervals.
We will also carry out exploratory analyses to examine the relationship between lower than expected blood levels and diagnostic and demographic patient characteristics.
This will help to inform future research projects and clinical initiatives.
Studietype
Observasjonsmessig
Registrering (Faktiske)
106
Kontakter og plasseringer
Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.
Studiesteder
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New York
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Glen Oaks, New York, Forente stater, 11004
- Zucker Hillside Hospital
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Deltakelseskriterier
Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
18 år og eldre (Voksen, Eldre voksen)
Tar imot friske frivillige
Nei
Kjønn som er kvalifisert for studier
Alle
Prøvetakingsmetode
Ikke-sannsynlighetsprøve
Studiepopulasjon
Adults with schizophrenia, schizoaffective disorder, or bipolar 1 disorder presenting to a psychiatric emergency room for acute psychosis and requiring inpatient hospital admission.
Beskrivelse
Inclusion Criteria:
- 18 years or older
- Documented diagnosis of schizophrenia, schizoaffective disorder, or bipolar 1 disorder
- Admitted to an inpatient psychiatric unit at Zucker Hillside Hospital for a psychotic decompensation.
- Outpatient for at least one month prior to admission
- On a regimen including risperidone, olanzapine, quetiapine, paliperidone or aripiprazole
Exclusion Criteria:
- Anti-psychotic polypharmacy
- Diagnosis of Mental Retardation or Pervasive Developmental Disorder
- Administrations of any of study medications in emergency room prior to blood draw.
Studieplan
Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.
Hvordan er studiet utformet?
Designdetaljer
Kohorter og intervensjoner
Gruppe / Kohort |
|---|
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Admitted Patients with Acute Psychosis
Patients 18 years of age or older with a documented diagnosis of schizophrenia, schizoaffective disorder, or bipolar 1 disorder who are admitted to an inpatient psychiatric unit at Zucker Hillside Hospital for a psychotic compensations.
Patients must have been in the outpatient setting for at least one month prior to admission on a regimen including risperidone, olanzapine, quetiapine, paliperidone or aripiprazole.
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
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Serum concentration of risperidone/9-OH-risperidone/olanzapine/quetiapine/aripiprazole
Tidsramme: 6 months
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6 months
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Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Sponsor
Etterforskere
- Hovedetterforsker: Leonardo V Lopez, M.D., Northwell Health
- Studieleder: John M Kane, M.D., Northwell Health
Studierekorddatoer
Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.
Studer hoveddatoer
Studiestart
1. februar 2013
Primær fullføring (Faktiske)
1. april 2015
Studiet fullført (Faktiske)
1. april 2015
Datoer for studieregistrering
Først innsendt
5. februar 2013
Først innsendt som oppfylte QC-kriteriene
5. februar 2013
Først lagt ut (Anslag)
7. februar 2013
Oppdateringer av studieposter
Sist oppdatering lagt ut (Anslag)
14. april 2015
Siste oppdatering sendt inn som oppfylte QC-kriteriene
13. april 2015
Sist bekreftet
1. april 2015
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- 11-384B
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