Eligibility Module

Eligibility Module

The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.

Eligibility Module path is as follows:

Study -> Protocol Section -> Eligibility Module

Eligibility Module


Ignite Creation Date: 2025-12-24 @ 9:55 PM
Ignite Modification Date: 2025-12-24 @ 9:55 PM
NCT ID: NCT02533232
Eligibility Criteria: Inclusion Criteria: * Male and female patients aged between 18-65 years, IQ \>70 (to complete assessments) identified by treating psychiatrist. * Confirmation of schizophrenia by using The MINI psychiatric interview (at baseline only) * Assessed as competent to provide informed consent by treating psychiatrist. * Antipsychotic medication has remained stable 4 weeks prior to baseline \*. Assessed as a partial responder to clozapine: patients prescribed clozapine at a stable therapeutic dose for a minimum of 3 months with total Positive and Negative Syndrome Schizophrenia (PANSS) score \>70. Exclusion Criteria: * Prior history of intolerance or serious side effects (hepatotoxicity, photosensitivity, blood dyscrasias) to any of the Tetracyclines. * Concomitant Penicillin therapy or concomitant anticoagulant therapy. * Active substance abuse (except nicotine or caffeine) or dependence within the last three months according to ICD 10 criteria. * Treatment with Warfarin or Lamotrigine. * Current or previous treatment with minocycline or other tetracycline antibiotics in the preceding three months before study entry. * Relevant current or past hematologic, hepatic, renal, neurological or other medical disorder that in the opinion of the principal investigator may interfere with the study. * Pregnant or breast-feeding females
Healthy Volunteers: False
Sex: ALL
Minimum Age: 18 Years
Maximum Age: 65 Years
Study: NCT02533232
Study Brief:
Protocol Section: NCT02533232