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Inositol Hexaphosphate: A Novel Treatment Strategy for Bipolar Disorder?

Primary Purpose

Bipolar Disorder, Manic Depression

Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
IP6
Lamotrigine
Sponsored by
San Diego Veterans Healthcare System
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Bipolar Disorder focused on measuring Bipolar Disorder, Depression, Inositol, Inositol Hexaphosphate, Phytic Acid, IP6, Lithium, Lamotrigine

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • must have bipolar disorder
  • must be currently depressed
  • must have failed adequate trial of lithium monotherapy
  • must have shown partial response of depression to lithium

Exclusion Criteria:

  • diagnoses of schizophrenia, major depression, or other psychotic disorder
  • currently pregnant
  • unstable medical condition
  • active drug or alcohol dependence
  • concurrent use of antidepressant or mood stabilizer other than lithium
  • active suicidal or homicidal ideation
  • past adverse reaction to lamotrigine or current skin rash (lamotrigine arm only)
  • history of dietary malabsorption or nutritional deficiency (IP6 arm only)

Sites / Locations

  • VA San Diego Healthcare System

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Lamotrigine

IP6

Arm Description

As adjunct to lithium therapy

As adjunct to lithium therapy

Outcomes

Primary Outcome Measures

Depression
As measured by rater administered Hamilton depression inventory, and Beck Depression Inventory

Secondary Outcome Measures

Sleep Quality
As measured by the Pittsburgh Sleep Quality Index
Global Function
As measured by the Clinician Global Inventory
Side Effect Burden
As measured by standardized inventory
Mania
As measured by the Young Mania Scale, and Internal State Scale

Full Information

First Posted
March 5, 2014
Last Updated
July 30, 2018
Sponsor
San Diego Veterans Healthcare System
Collaborators
The Depressive and Bipolar Disorder Alternative Treatment Foundation
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1. Study Identification

Unique Protocol Identification Number
NCT02081287
Brief Title
Inositol Hexaphosphate: A Novel Treatment Strategy for Bipolar Disorder?
Official Title
Inositol Hexaphosphate: A Novel Treatment Strategy for Bipolar Disorder?
Study Type
Interventional

2. Study Status

Record Verification Date
July 2018
Overall Recruitment Status
Completed
Study Start Date
May 2014 (undefined)
Primary Completion Date
July 30, 2018 (Actual)
Study Completion Date
July 30, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
San Diego Veterans Healthcare System
Collaborators
The Depressive and Bipolar Disorder Alternative Treatment Foundation

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Inositol hexaphosphate (IP6, also called inositol hexakisphosphate, and phytic acid) is a naturally occurring phosphorylated derivative of myo-inositol. Myo-inositol has shown preliminary evidence of efficacy in controlling mood symptoms, and good tolerability in bipolar disorder in some studies, but failed to establish efficacy in subsequent meta-analyses. In the investigators proposed work, the investigators plan to orally administer the calcium/magnesium salt of IP6 (2,000-3,000 mg daily in two divided doses) to paid research subjects with a diagnosis of bipolar disorder who are in a depressed state, and who have failed an adequate course of treatment with lithium monotherapy. The investigators hypothesis is that IP6 may be similar to myo-inositol in terms of relieving depression, but more potent and effective. Our aim is conduct a preliminary pilot study in 30 subjects (15 treated with IP6, 15 treated with lamotrigine, an active comparator) to assess the efficacy and tolerability of IP6 as an adjunctive treatment to lithium, the mood stabilizer most commonly used to treat bipolar disorder.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bipolar Disorder, Manic Depression
Keywords
Bipolar Disorder, Depression, Inositol, Inositol Hexaphosphate, Phytic Acid, IP6, Lithium, Lamotrigine

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
8 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Lamotrigine
Arm Type
Active Comparator
Arm Description
As adjunct to lithium therapy
Arm Title
IP6
Arm Type
Experimental
Arm Description
As adjunct to lithium therapy
Intervention Type
Drug
Intervention Name(s)
IP6
Other Intervention Name(s)
Inositol Hexaphosphate, Phytic Acid
Intervention Description
IP6 2,000 -3,000 mg per day given orally in two doses
Intervention Type
Drug
Intervention Name(s)
Lamotrigine
Other Intervention Name(s)
Lamictal
Intervention Description
Dose up to 200 mg per day over 10 weeks
Primary Outcome Measure Information:
Title
Depression
Description
As measured by rater administered Hamilton depression inventory, and Beck Depression Inventory
Time Frame
10 weeks
Secondary Outcome Measure Information:
Title
Sleep Quality
Description
As measured by the Pittsburgh Sleep Quality Index
Time Frame
10 weeks
Title
Global Function
Description
As measured by the Clinician Global Inventory
Time Frame
10 weeks
Title
Side Effect Burden
Description
As measured by standardized inventory
Time Frame
10 weeks
Title
Mania
Description
As measured by the Young Mania Scale, and Internal State Scale
Time Frame
10 weeks
Other Pre-specified Outcome Measures:
Title
Morning vs Evening Preference
Description
As measured by the Basic language morningness scale
Time Frame
10 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: must have bipolar disorder must be currently depressed must have failed adequate trial of lithium monotherapy must have shown partial response of depression to lithium Exclusion Criteria: diagnoses of schizophrenia, major depression, or other psychotic disorder currently pregnant unstable medical condition active drug or alcohol dependence concurrent use of antidepressant or mood stabilizer other than lithium active suicidal or homicidal ideation past adverse reaction to lamotrigine or current skin rash (lamotrigine arm only) history of dietary malabsorption or nutritional deficiency (IP6 arm only)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michael J. McCarthy, MD, PhD
Organizational Affiliation
VA San Diego Healthcare, UCSD
Official's Role
Principal Investigator
Facility Information:
Facility Name
VA San Diego Healthcare System
City
San Diego
State/Province
California
ZIP/Postal Code
92161
Country
United States

12. IPD Sharing Statement

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Inositol Hexaphosphate: A Novel Treatment Strategy for Bipolar Disorder?

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