Evidence map›Paper›PMID 25886254›Full record

Trial reportTrials2015

The benefit of minocycline on negative symptoms in early-phase psychosis in addition to standard care - extent and mechanism (BeneMin): study protocol for a randomised controlled trial.

Danuta M Lisiecka, John Suckling, Thomas R E Barnes, Imran B Chaudhry, Paola Dazzan, Nusrat Husain, Peter B Jones, Eileen M Joyce, Stephen M Lawrie, Rachel Upthegrove and 1 more

Registry-linked trialOpen access · goldAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Trials, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02907437 (Minocycline add-on Medication to Antipsychotics in the Treatment of Schizophrenia Patients), which is not on this map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.4field-weighted citation impact, top 44% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT02907437 phase3unknown statusnot on this map

Minocycline add-on Medication to Antipsychotics in the Treatment of Schizophrenia Patients: A Double- Blind Randomized Controlled Trial

TypeinterventionalSponsorBeer Yaakov - Ness Ziona Mental Health CenterRan2015 to 2018Enrolled40ConditionsSchizophreniaArmsMinocycline, Placebo, Probiotics
3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Treating Negative Symptoms in Schizophrenia: an Update.Current treatment options in psychiatry
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 8 institutions in 1 country.

Danuta M LisieckaDepartment of Psychiatry, Behavioural and Clinical Neuroscience Institute, University of Cambridge, Cambridge, UK. dml45@cam.ac.uk.
John SucklingDepartment of Psychiatry, Behavioural and Clinical Neuroscience Institute, University of Cambridge, Cambridge, UK. js369@cam.ac.uk.
Thomas R E BarnesDepartment of Medicine, Centre for Mental Health, Faculty of Medicine, Imperial College, London, UK. t.r.barnes@imperial.ac.uk.
Imran B ChaudhryInstitute of Brain, Behaviour and Mental Health, Clinical and Cognitive Neurosciences, University of Manchester, Manchester, UK. imran.chaudhry@manchester.ac.uk.
Paola DazzanDepartment of Psychosis Studies, Institute of Psychiatry, King's College, London, UK. paola.dazzan@kcl.ac.uk.
Nusrat HusainInstitute of Brain, Behaviour and Mental Health, Clinical and Cognitive Neurosciences, University of Manchester, Manchester, UK. nusrat.husain@manchester.ac.uk.
Peter B JonesCambridge and Peterborough NHS Foundation Trust, Cambridge, UK. pbj21@cam.ac.uk.
Eileen M JoyceInstitute of Neurology, University College London, London, UK. e.joyce@ucl.ac.uk.
Stephen M LawrieDivision of Psychiatry, University of Edinburgh, Royal Edinburgh Hospital, Edinburgh, UK. S.Lawrie@ed.ac.uk.
Rachel UpthegroveSchool of Clinical and Experimental Medicine, University of Birmingham, Birmingham, UK. r.upthegrove@bham.ac.uk.
Bill DeakinInstitute of Brain, Behaviour and Mental Health, Clinical and Cognitive Neurosciences, University of Manchester, Manchester, UK. bill.deakin@manchester.ac.uk.
University of Manchester · GBUniversity of Cambridge · GBCambridgeshire and Peterborough NHS Foundation Trust · GBKing's College London · GBRoyal Edinburgh Hospital · GBUniversity College London · GBUniversity of Birmingham · GBWest London Mental Health NHS Trust · GB

Funding

Medical Research Council MC_PC_11003
6 · The paper itself

Abstract

backgroundNegative symptoms of psychosis do not respond to the traditional therapy with first- or second-generation antipsychotics and are among main causes of a decrease in quality of life observed in individuals suffering from the disorder. Minocycline, a broad-spectrum tetracyclic antibiotic displaying neuroprotective properties has been suggested as a new potential therapy for negative symptoms. In the two previous clinical trials comparing minocycline and placebo, both added to the standard care, patients receiving minocycline showed increased reduction in negative symptoms. Three routes to neuroprotection by minocycline have been identified: neuroprotection against grey matter loss, anti-inflammatory action and stabilisation of glutamate receptors. However, it is not yet certain what the extent of the benefit of minocycline in psychosis is and what its mechanism is. We present a protocol for a multi-centre double-blind randomised placebo-controlled clinical trial entitled The Benefit of Minocycline on Negative Symptoms of Psychosis: Extent and Mechanism (BeneMin).

methodsAfter providing informed consent, 226 participants in the early phase of psychosis will be randomised to receive either 100 mg modified-release capsules of minocycline or similar capsules with placebo for 12 months in addition to standard care. The participants will be tested for outcome variables before and after the intervention period. The extent of benefit will be tested via clinical outcome measures, namely the Positive and Negative Syndrome Scale score, social and cognitive functioning scores, antipsychotic medication dose equivalent and level of weight gain. The mechanism of action of minocycline will be tested via blood screening for circulating cytokines and magnetic resonance imaging with three-dimensional T1-weighted rapid gradient-echo, proton density T2-weighted dual echo and T2*-weighted gradient echo planar imaging with N-back task and resting state. Eight research centres in UK and 15 National Health Service Trusts and Health Boards will be involved in recruiting participants, performing the study and analysing the data. DISCUSSION: The BeneMin trial can inform as to whether in minocycline we have found a new and effective therapy against negative symptoms of psychosis. The European Union Clinical Trial Register: EudraCT 2010-022463-35 with the registration finalised in July 2011. The recruitment in the trial started in January 2013 with the first patient recruited in March 2013.

Indexed as

Clinical ProtocolsDouble-Blind MethodHumansMagnetic Resonance ImagingMinocyclineNeuroprotective AgentsOutcome Assessment, Health CarePsychotic DisordersMinocyclineNeuroprotective Agents

Identifiers

PMID25886254
PMCPMC4351843
OpenAlexW2061187735

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.