The Benefit of Minocycline on Negative Symptoms in Schizophrenia: Extent and Mechanisms

NCT02928965 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 207

Last updated 2019-04-18

No results posted yet for this study

Summary

The purpose of this study is to investigate if minocycline limits the development of negative symptoms in early psychosis and to test via what mechanism of action this change occurs.

Conditions

  • Schizophrenia and Disorders With Psychotic Features

Interventions

DRUG

Minocycline

Capsules containing 100mg minocycline (modified release), administered orally by the patient, two per day for the first two weeks and then three per day for the reminder of the 12 month treatment period in addition to standard therapy.

DRUG

Placebo

Matching placebo with appearance of over - encapsulated minocycline

Sponsors & Collaborators

  • University of Edinburgh

    collaborator OTHER
  • University of Cambridge

    collaborator OTHER
  • University College, London

    collaborator OTHER
  • University of Birmingham

    collaborator OTHER
  • King's College London

    collaborator OTHER
  • Manchester Mental Health & Social Care Trust

    collaborator OTHER_GOV
  • Greater Manchester Mental Health NHS Foundation Trust

    collaborator OTHER
  • Northern Care Alliance NHS Foundation Trust

    collaborator OTHER
  • Lancashire Care NHS Foundation Trust

    collaborator NETWORK
  • Cambridgeshire and Peterborough NHS Foundation Trust

    collaborator OTHER
  • West London Mental Health NHS Trust

    collaborator OTHER
  • North East London Foundation Trust

    collaborator OTHER
  • Central and North West London NHS Foundation Trust

    collaborator OTHER
  • Camden and Islington NHS Foundation Trust

    collaborator UNKNOWN
  • South London and Maudsley NHS Foundation Trust

    collaborator OTHER
  • NHS Lothian

    collaborator OTHER_GOV
  • NHS Fife

    collaborator OTHER_GOV
  • NHS Borders

    collaborator OTHER_GOV
  • University Hospital Birmingham NHS Foundation Trust

    collaborator OTHER
  • University of Manchester

    lead OTHER

Principal Investigators

  • Bill Deakin, Professor · University of Manchester

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
16 Years
Max Age
35 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-02-28
Primary Completion
2016-05-31
Completion
2016-05-31

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02928965 on ClinicalTrials.gov