Study of Mirtazapine for Agitation in Dementia

Dementia Clinical Trial

— SYMBAD  

Official title:

A Pragmatic, Multi Centre, Double-blind, Placebo Controlled Randomised Trial to Assess the Safety, Clinical and Cost Effectiveness of Mirtazapine in Patients With Alzheimer's Disease (AD) and Agitated Behaviours

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03031184
• Other study ID #: 15/SC/0606
• Status: Completed
• Phase: Phase 3
• Start date: January 2017
• Est. completion date: March 2021

Study information

• Verified date: April 2021
• Source: University of Sussex
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This clinical trial evaluates whether Mirtazapine is more effective than placebo in treating agitation in people with dementia. The trial will assess the safety, clinical and cost effectiveness of the treatment. Participants will be randomised to receive either Mirtazapine or placebo for 12 weeks and will be followed up for up to one year, in this blinded trial.

Description:

Patient-centred care, without the use of medicines is offered as a first course of treatment for agitation in dementia. However, there is a need for second line treatments when these fail, at the moment antipsychotics are commonly prescribed, as very little research has been done in to safer alternative treatments.

There are medicines available to treat agitation and/or aggression in dementia, but it is not clear which treatments work best.

This research study has been designed to help answer this, by comparing a which is currently prescribed for depression, Mirtazapine, with placebo (a tablet designed to look like a medicine but that has no active medicine in it) to see if Mirtazapine is suitable for treating agitation in dementia.

If participants and their family/carers agree to take part in this study, participants will be prescribed treatment for 12 weeks. Participants will then be followed up for 1 year after, with assessment sessions at 26 and 52 weeks.

Participants taking part in this study will be randomly allocated to a treatment group (selected to their treatment group by chance). The study is blinded, so this means the participant's doctor and the research team will not know which treatment the participant has been taking until after the study has ended. This is necessary so that the trial is a fair test of which treatment works best, however it is possible to find out which medicine they are taking in the event of a medical emergency.

The study is entirely voluntary and all participants wishing to join the study must complete an informed consent form (or if they lack capacity the participant's representative may do so on their behalf). Each participant must also have a nominated carer who consents to being questioned on aspects of the participant's dementia/care and their own experiences in caring for the participant.

The investigators are aiming to recruit 222 patients to the study in total from around 20 different regions across the UK.

The study was originally designed to included a second medication, called Carbamazepine, to also look at whether it would work and be safe and cost effective in agitation in dementia. Challenges in recruitment in this population resulted in the funder requesting that the available data was reviewed to July 2018, to see whether one of the arms (Mirtazapine or Carbamazepine) should be discontinued in terms of future recruitment. The independent data monitoring committee compared blinded data from both groups against placebo data and concluded that on the basis of efficacy and safety, the group, which when unblinded was found to be Carbamazepine, should be dropped. Some limited analysis will still be completed for all data collected in the Carbamazepine group, but the trial will continue now only randomising participants to Mirtazapine or placebo.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 207
• Est. completion date: March 2021
• Est. primary completion date: June 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Patients with a clinical diagnosis of probable or possible Alzheimer's Disease using National Institute of Neurological and Communicative Disorders and Stroke and the Alzheimer's Disease and Related Disorders Association (NINCDS/ADRDA) criteria (McKhann et Al, 1984)

• a diagnosis of co-existing agitated behaviours

• evidence that the agitated behaviours have not responded to management according to the AS/DH algorithm (AS/DH, 2011)

• An assessment of Cohen Mansfield Agitation Inventory (CMAI; Cohen-Mansfield et al, 1989, Long form) score of 45 or greater

• Written informed consent to enter and be randomised into the trial

• Availability of a suitable informant (consenting identifiable family carer or paid carer) to provide information on carer-completed outcome measures and who consents to take part in the trial.

Exclusion Criteria:

• Current treatment with antidepressants (including MAOIs) or antipsychotics. Normal clinical practice should be followed, with an appropriate washout period before trial drug administration. For MAOIs this should be least two weeks.

• Contraindications to the administration of mirtazapine as per the current SmPC

• Patients with second degree atrioventricular block (patients with third degree heart block, with a pace maker fitted, may be included at PI discretion)

• Cases too critical for randomisation (ie where there is a suicide risk or where the patient presents a risk of harm to others)

• Female subjects under the age of 55 of childbearing potential, defined as follows:

postmenopausal females who have not had at least 12 months of spontaneous amenorrhea or 6 months of spontaneous amenorrhoea with serum FSH>40mIU/ml or females who have not had a hysterectomy or bilateral oophorectomy at least 6 weeks prior to enrolment.

Related Conditions & MeSH terms

• Dementia

Intervention

Drug:
• Mirtazapine

Other:
• Placebo

Locations

Country	Name	City	State
United Kingdom	Sube Banerjee	Brighton	Sussex

Sponsors (11)

Lead Sponsor	Collaborator
University of Sussex	Alzheimer's Society, Birmingham and Solihull Mental Health NHS Foundation Trust, London School of Economics and Political Science, Norwich Clinical Trials Unit, The Centre for Dementia Studies, Brighton and Sussex Medical School and SPFT, University College, London, University of Cambridge, University of East Anglia, University of Manchester, University of Newcastle Upon-Tyne

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Cohen Mansfield Agitation Inventory (CMAI) score (Long Form, 29 questions)	Measured at baseline, 6 and 12 weeks, it is the difference in the score at 12 weeks that is the primary outcome. The questions are asked of the person with dementia's carer	Baseline, 6 weeks, 12 weeks