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Histamine H2 Antagonism as Adjuvant Therapy in Treatment Resistant Schizophrenia

Histamine H2 Antagonism as Adjuvant Therapy in Treatment Resistant Schizophrenia

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00565175
Enrollment
30
Registered
2007-11-29
Start date
2008-01-31
Completion date
2011-12-31
Last updated
2012-03-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Schizophrenia

Keywords

Treatment resistant, Chronic

Brief summary

The purpose of the study is to investigate whether blockade of the histamine H2 receptors in the brain will have any beneficial effect on the symptoms of subjects with schizophrenia.

Detailed description

Histamine functions as a neurotransmitter in the brain. It has an important role as modulator of the release of other neurotransmitters, including dopamine. The histamine receptors are widely expressed in the brain, H1 and H2 receptors are post-synaptic, H3 a pre-synaptic autoreceptor. There is an abundance of neurobiologic data from animal and human studies supporting the role of histamine in the pathogenesis and treatment of psychoses. In 1990 a case report of a treatment resistant subject with schizophrenia whos symptoms improved markedly when he was prescribed a H2 antagonist because of peptic ulcer. Later, a open-label trial including 18 patients has been performed, reporting significant symptom reduction, especially on negative symptoms. Also the subjective comments both by the subjects and the investigators in that study were optimistic and suggested an effect primarily on negative symptoms. The present study will be the first double-blind, randomized, placebo controlled, parallel group study of the subject matter. The study focuses on treatment resistant schizophrenia cases in the stable phase.

Interventions

DRUGfamotidine

Capsules containing 100 mg of famotidine p.o., twice daily for 4 weeks.

DRUGPlacebo (Microcrystallized cellulose)

Placebo administered in identical capsules as the experimental drug.

Sponsors

Finland: Lilly saatio foundation
CollaboratorUNKNOWN
Jesper Ekelund
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Diagnosis of schizophrenia assessed by SCID-I (DSM-IV) as well as RDC-criteria * Patient record mention of schizophrenia (ICD-10) at least 5 years previously * Disability pension due to psychiatric disorder * At least 3 points on the CGI scale

Exclusion criteria

* Epilepsy or a history of unclear seizures * Stroke * Parkinson's disease * AIDS * Substance addiction or abuse within 3 months prior to enrolment. * Individuals who are deemed at risk for aggressive behavior or suicide by their clinician * Pregnant and breast-feeding subjects * Serious unstable physical illness * Persons who have been deemed legally incapacitated according to Finnish law (Laki holhoustoimesta 1.4.1999/442, 3. luku, 18 §) * Individuals who use H2-antagonists as prescribed by a physician * Known allergy to famotidine or any other component of the Pepcidin® 40 mg tablet * Glomerular Filtration Rate (GFR) according to the Cockcroft-Gault formula \< 30 ml/min

Design outcomes

Primary

MeasureTime frame
Scale for the Assessment of Negative Symptoms (SANS) score5 weeks

Secondary

MeasureTime frame
Positive and Negative Syndrome Scale (PANSS) score5 weeks
Clinical Global Impression (CGI) score5 weeks

Countries

Finland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026