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Histamine H2 Antagonism as Adjuvant Therapy in Treatment Resistant Schizophrenia

Primary Purpose

Schizophrenia

Status
Completed
Phase
Phase 4
Locations
Finland
Study Type
Interventional
Intervention
famotidine
Placebo (Microcrystallized cellulose)
Sponsored by
Jesper Ekelund
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Schizophrenia focused on measuring Treatment resistant, Chronic

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • HUCH Department of Psychiatry
  • Kellokosken sairaala
  • Lohjan sairaanhoitoalue
  • Vaasa Hospital District
  • Peijaksen sairaala

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

famotidine

Placebo

Arm Description

Outcomes

Primary Outcome Measures

Scale for the Assessment of Negative Symptoms (SANS) score

Secondary Outcome Measures

Positive and Negative Syndrome Scale (PANSS) score
Clinical Global Impression (CGI) score

Full Information

First Posted
November 28, 2007
Last Updated
March 19, 2012
Sponsor
Jesper Ekelund
Collaborators
Finland: Lilly saatio foundation
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1. Study Identification

Unique Protocol Identification Number
NCT00565175
Brief Title
Histamine H2 Antagonism as Adjuvant Therapy in Treatment Resistant Schizophrenia
Official Title
Histamine H2 Antagonism as Adjuvant Therapy in Treatment Resistant Schizophrenia
Study Type
Interventional

2. Study Status

Record Verification Date
March 2012
Overall Recruitment Status
Completed
Study Start Date
January 2008 (undefined)
Primary Completion Date
December 2011 (Actual)
Study Completion Date
December 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Jesper Ekelund
Collaborators
Finland: Lilly saatio foundation

4. Oversight

Data Monitoring Committee
No

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Schizophrenia
Keywords
Treatment resistant, Chronic

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
30 (Actual)

8. Arms, Groups, and Interventions

Arm Title
famotidine
Arm Type
Experimental
Arm Title
Placebo
Arm Type
Placebo Comparator
Intervention Type
Drug
Intervention Name(s)
famotidine
Other Intervention Name(s)
Famotidin Hexal
Intervention Description
Capsules containing 100 mg of famotidine p.o., twice daily for 4 weeks.
Intervention Type
Drug
Intervention Name(s)
Placebo (Microcrystallized cellulose)
Other Intervention Name(s)
Microcrystallized cellulose
Intervention Description
Placebo administered in identical capsules as the experimental drug.
Primary Outcome Measure Information:
Title
Scale for the Assessment of Negative Symptoms (SANS) score
Time Frame
5 weeks
Secondary Outcome Measure Information:
Title
Positive and Negative Syndrome Scale (PANSS) score
Time Frame
5 weeks
Title
Clinical Global Impression (CGI) score
Time Frame
5 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jesper Ekelund, MD-PhD
Organizational Affiliation
Helsinki University Central Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
HUCH Department of Psychiatry
City
Helsinki
ZIP/Postal Code
10029
Country
Finland
Facility Name
Kellokosken sairaala
City
Kellokoski
ZIP/Postal Code
04500
Country
Finland
Facility Name
Lohjan sairaanhoitoalue
City
Lohja
ZIP/Postal Code
08450
Country
Finland
Facility Name
Vaasa Hospital District
City
Vaasa
Country
Finland
Facility Name
Peijaksen sairaala
City
Vantaa
ZIP/Postal Code
01450
Country
Finland

12. IPD Sharing Statement

Citations:
PubMed Identifier
23764683
Citation
Meskanen K, Ekelund H, Laitinen J, Neuvonen PJ, Haukka J, Panula P, Ekelund J. A randomized clinical trial of histamine 2 receptor antagonism in treatment-resistant schizophrenia. J Clin Psychopharmacol. 2013 Aug;33(4):472-8. doi: 10.1097/JCP.0b013e3182970490.
Results Reference
derived

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Histamine H2 Antagonism as Adjuvant Therapy in Treatment Resistant Schizophrenia

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