Quetiapine Extended Release (XR) for the Management of Psychotic Aggression or Agitation in Adult Acute Psychiatry

NCT ID: NCT00986167

Last Updated: 2009-09-29

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE4
• Total Enrollment: 72 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2009-10-31
• Study Completion Date: 2010-10-31

Brief Summary

This study is a multi-site study examining the use of Quetiapine XR for psychotic aggression in an acute psychiatric setting. The study aims to demonstrate that management with Quetiapine XR significantly reduces aggressive behaviour in acute patients with psychosis, significantly reduces psychotic symptoms and decreases the requirement for sedation using benzodiazepines.

Detailed Description

Aggression is a common occurrence in acute psychiatry as the experience of schizophrenia or related psychotic symptoms significantly increases the risk of aggressive behaviour. This can have detrimental effects on the provision of therapy and safety for staff and other patients.

Current practice in managing aggression in acute psychiatry often involves the addition of a sedating antipsychotic or benzodiazepine to a main atypical antipsychotic that is continued as a primary treatment.

Quetiapine IR (immediate release) has been found effective in the treatment and management of schizophrenia. Quetiapine acts in the brain on cell receptors to which serotonin (a chemical produced in the brain) binds. Serotonin is proposed to play a significant role in impulsive aggression. Additionally, sedation is a side effect of Quetiapine, which may also facilitate its use in aggression. However, Quetiapine is not commonly used in the management of aggression in acute psychiatry due to the amount of time required to achieve an optimal dose (up to 5 days).

Quetiapine XR (extended release) is an extended release formulation of Quetiapine that can be initiated at a higher dose, a therapeutic dose can be achieved more rapidly and is taken once per day instead of twice.

This study is a multi-site study examining the use of Quetiapine XR for psychotic aggression in an acute psychiatric setting. The study aims to demonstrate that management with Quetiapine XR significantly reduces aggressive behaviour in acute patients with psychosis, significantly reduces psychotic symptoms and decreases the requirement for sedation using benzodiazepines.

The participants will be in-patients experiencing psychotic aggression (determined by psychiatrist). For those patients experiencing aggression (which is not severe enough to require intramuscular injection), the treating clinician will make a decision whether or not to treat with Quetiapine XR. Those patients meeting inclusion/exclusion criteria will be observed over 8 days using measures that rate symptoms, aggression and possible side effects (these include observation, questionnaire and review of patient files).

Conditions

Schizophrenia; Psychosis

Keywords

Psychosis; Aggression; Acute; Quetiapine XR

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Quetiapine XR

The study population will be patients admitted to the acute psychiatry inpatient wards of St Vincent's or the Alfred and determined by a Psychiatrist to be experiencing a psychotic illness (including mania with psychotic features and drug-induced psychosis) and acting in an aggressive manner (determined by a score of at least 1 on the OAS).

Group Type: EXPERIMENTAL

Quetiapine XR

Intervention Type: DRUG

The daily dose of oral Quetiapine XR at the start of therapy is 300 mg on Day 1, 600 mg on Day 2 and up to 800 mg after Day 2. The dose will be adjusted within the usual effective dose range of 400 to 800 mg/day, depending on the clinical response and tolerability of the individual patient.

Interventions

Quetiapine XR

The daily dose of oral Quetiapine XR at the start of therapy is 300 mg on Day 1, 600 mg on Day 2 and up to 800 mg after Day 2. The dose will be adjusted within the usual effective dose range of 400 to 800 mg/day, depending on the clinical response and tolerability of the individual patient.

Intervention Type: DRUG

Other Intervention Names

Seroquel XR

Eligibility Criteria

Inclusion Criteria

1. Males or Females aged 18-65 years;

2. Determined by a psychiatrist to be experiencing acute psychotic symptoms (includes mania with psychotic features and drug-induced psychosis);

3. Determined by a psychiatrist to have acted aggressively (score of > 1 on the OAS);

4. Inpatient status at enrollment;

5. Patient agreement to take oral medication;

6. Provision of written informed consent when considered able to provide consent by the treating team;

7. Female patients of childbearing potential must be using a reliable method of contraception and have a negative urine human chorionic gonadotropin (HCG) test at enrollment.

3. Patients who, in the opinion of the investigator, pose an imminent risk of suicide or a danger to self or others;

4. Known intolerance or lack of response to quetiapine fumarate or any other atypical psychotics, as judged by the investigator;

5. Use of any of the following cytochrome P450 3A4 inhibitors in the 14 days preceding enrolment including but not limited to: ketoconazole, itraconazole, fluconazole, erythromycin, clarithromycin, troleandomycin, indinavir, nelfinavir, ritonavir, fluvoxamine and saquinavir;

6. Use of any of the following cytochrome P450 inducers in the 14 days preceding enrolment including but not limited to: phenytoin, carbamazepine, barbiturates, rifampin, St. John's Wort, and glucocorticoids;

7. Administration of a depot antipsychotic injection within one dosing interval (for the depot) prior to being recruited for the trial;

8. Patients receiving treatment with an antipsychotic other than Seroquel XR (either IM or oral) within one dosing interval prior to being recruited for the trial;

9. Patients receiving treatment with mood stabiliser or anti-depressant medication within 7 days prior to treatment with Seroquel XR;

10. Substance or alcohol abuse or dependence at enrolment (except dependence in full remission, and except for caffeine or nicotine dependence), as defined by DSM-IV criteria;

11. Medical conditions that would affect absorption, distribution, metabolism, or excretion of study treatment;

12. Unstable or inadequately treated renal, hepatic, cardiovascular, respiratory, cerebrovascular, or other serious progressive physical disease as judged by the investigator;

13. Involvement in the planning and conduct of the study;

14. Previous enrolment in the present study;

15. Participation in another drug trial within 4 weeks prior enrolment into this study or longer in accordance with local requirements;

16. A patient with Diabetes Mellitus (DM) fulfilling one of the following criteria:

• Unstable DM defined as enrolment glycosylated hemoglobin (HbA1c) >8.5%;
• Admitted to hospital for treatment of DM or DM related illness in past 12 weeks;
• Not under physician care for DM;
• Physician responsible for patient's DM care has not indicated that patient's DM is controlled;
• Physician responsible for patient's DM care has not approved patient's participation in the study;
• Has not been on the same dose of oral hypoglycaemic drug(s) and/or diet for the 4 weeks prior to randomisation. For thiazolidinediones (glitazones) this period should not be less than 8 Weeks;
• Taking insulin whose daily dose on one occasion in the past 4 weeks has been more than 10% above or below their mean dose in the preceding 4 weeks.

17. An absolute neutrophil count (ANC) of > 1.5 x 109 per liter;

18. Refusal to take oral medication and intramuscular antipsychotic medication is administered instead.

Exclusion Criteria

1. Pregnancy or lactation;

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

AstraZeneca

INDUSTRY

Sponsor Role: collaborator

Bayside Health

OTHER_GOV

Sponsor Role: lead

Responsible Party

Bayside Health

Principal Investigators

Jayashri Kulkarni, Prof

Role: PRINCIPAL_INVESTIGATOR

Alfred Psychiatry Research Centre

Locations

St Vincent's Hospital, Melbourne

Fitzroy, Victoria, Australia

Alfred Psychiatry Research Centre

Melbourne, Victoria, Australia

Countries

Australia

Facility Contacts

David Castle

Role: primary

Peter Bosanac

Role: backup

Jayashri Kulkarni, Prof.

Role: primary

Anthony de Castella

Role: backup

Other Identifiers

D1443C00043

Identifier Type: -

Identifier Source: org_study_id