Intranasal Ketamine In the Treatment of Pediatric Bipolar Disorder (IKBP)
Primary Purpose
Bipolar Disorder
Status
Terminated
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Ketamine hydrochloride injection
Flat tonic water (e.g., Canada Dry Tonic Water)
Sponsored by
About this trial
This is an interventional treatment trial for Bipolar Disorder focused on measuring bipolar disorder, treatment resistance, depression, ketamine, intranasal, child
Eligibility Criteria
Inclusion Criteria:
- Males and females aged 6-12;
- DSM-IV bipolar disorder (BPI, BPII, BP-NOS, BP-FOH);
- Treatment resistant - as defined by failure to adequately respond to at least 2 different classes of medications such as mood stabilizers and antipsychotic agent.
Exclusion Criteria:
- Contraindication to the use of ketamine, including allergy and current use of medicine contraindicated with ketamine;
- Endocrine or neurological illness;
- Previous history of closed head injury, current head injury associated with possible intracranial hypertension, central nervous system masses, abnormalities, or hydrocephalus, ever had loss of consciousness;
- Previous history of glaucoma or acute globe injury
- Abnormal nasal physiology which would not allow for adequate medication delivery;
- Any change in medication type or dose within the past 30 days;
- Treatment with any MAOI's currently or within the past 3 months;
- Has had a course of ECT within the past 3 months;
- Has ever used PCP or ketamine;
- Meets DSM-IV criteria for Mental Retardation;
- Has ever had Repetitive Transcranial Magnetic Stimulation (rTMS), Vagal Nerve Stimulation (VNS) or Deep Brain Stimulation;
- Is currently hospitalized;
- Has known or suspected schizophrenia, even if currently stable or controlled with medications
- Is acutely suicidal or homicidal (i.e., in imminent danger with plan, urges and intent to harm oneself or others) including any serious attempts/those requiring hospitalization in the past 12 months or at the PI's discretion;
- The presence of any abnormal laboratory findings or serious medical disorder or condition including: clinically significant organ system dysfunction; significant endocrine disease, including diabetes mellitus; hypothyroidism; cardiovascular disease (myocardial ischemia, heart failure, arrhythmias); coagulopathy; significant anemia; significant acute infection; glaucoma; dehydration; epilepsy; any intra-abdominal or intrathoracic surgery or limb amputation within the prior 6 months; any diagnosed cardiac condition causing documented hemodynamic compromise or dysfunction of the SA or AV node; any diagnosed respiratory condition causing documented or clinically recognized hypoxia (e.g., chronic obstructive or restrictive pulmonary disease); body weight approximately < 80% or > 120% ideal body weight; or any medical condition known to interfere with cognitive performance; medication-related exclusions include narcotic therapy, chronic acetaminophen use, acute sedative hypnotic withdrawal, corticosteroid or spironolactone therapy, regularly dosed narcotics or any other sedative therapy or medication that interferes with SA or AV node function or could be considered contraindicated with the sedative properties of ketamine.
Sites / Locations
- Individual homes of subjects
- Juvenile Bipolar Research Foundation
- Individual homes of subjects
- Individual homes of subjects
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Placebo Comparator
Arm Label
Bipolar-Ketalar
Bipolar-Placebo
Arm Description
Children with a diagnosis of BP-I, BP-II or BP-NOS will receive 4 administrations of intranasal ketalar
Children with a diagnosis of BP-I, BP-II or BP-NOS will receive 4 administrations of placebo
Outcomes
Primary Outcome Measures
Young Mania Rating Scale
Young Mania Rating Scale
Young Mania Rating Scale
Young Mania Rating Scale
Overt Aggression Scale
Overt Aggression Scale
Overt Aggression Scale
Overt Aggression Scale
Yale Brown Obsessive Compulsive Scale
Secondary Outcome Measures
Wechsler Intelligence Scale for Children-IV
Peripheral Thermal Challenge
body temperature
A proprietary ambulatory monitor will measure skin and tympanic temperature using conventional thermistors and IR sensors
Triaxial acceleration
A proprietary ambulatory monitor will measure triaxial acceleration from the forehead using a commercially-available sensor that also provides a plethysmograph signal from which heart rate can be derived.
SpO2
A proprietary ambulatory monitor will measure triaxial acceleration from the forehead using a commercially-available sensor that also provides a plethysmograph signal from which heart rate can be derived.
Galvanic skin response
A proprietary ambulatory monitor will measure galvanic skin response obtained with two conventional electrodes.
Delis-Kaplin Executive Function System
Conner's Continuous Performance Test
SCARED
Full Information
NCT ID
NCT01504659
First Posted
January 3, 2012
Last Updated
March 14, 2017
Sponsor
Juvenile Bipolar Research Foundation
1. Study Identification
Unique Protocol Identification Number
NCT01504659
Brief Title
Intranasal Ketamine In the Treatment of Pediatric Bipolar Disorder
Acronym
IKBP
Official Title
Intranasal Ketamine In the Treatment of Pediatric Bipolar Disorder
Study Type
Interventional
2. Study Status
Record Verification Date
March 2017
Overall Recruitment Status
Terminated
Why Stopped
Administrative issues
Study Start Date
July 2012 (undefined)
Primary Completion Date
November 2016 (Actual)
Study Completion Date
November 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Juvenile Bipolar Research Foundation
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The investigators plan to evaluate the efficacy and safety of intranasal Ketalar (ketamine hydrochloride) in the treatment of primary symptom manifestations of pediatric bipolar disorder; Fear of Harm (FOH) phenotype. This phenotype represents those children who are most resistant to traditional treatments and suffer repeated hospitalizations. Primary symptoms include fearfulness, aggression secondary to threat, mood and/or arousal instability, and psychosis. In addition to evaluation of efficacy and safety, the investigators will also analyze whether therapeutic response depends upon the degree to which the subject fits the FOH phenotype.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bipolar Disorder
Keywords
bipolar disorder, treatment resistance, depression, ketamine, intranasal, child
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderOutcomes Assessor
Allocation
Randomized
Enrollment
5 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Bipolar-Ketalar
Arm Type
Active Comparator
Arm Description
Children with a diagnosis of BP-I, BP-II or BP-NOS will receive 4 administrations of intranasal ketalar
Arm Title
Bipolar-Placebo
Arm Type
Placebo Comparator
Arm Description
Children with a diagnosis of BP-I, BP-II or BP-NOS will receive 4 administrations of placebo
Intervention Type
Drug
Intervention Name(s)
Ketamine hydrochloride injection
Other Intervention Name(s)
Ketalar NDA 016812, Ketamine Hydrochloride Injection, Abbot Hospital, 074549, Ketamine Hdyrochloride Injection, Bioniche, 076092, Ketamine Hydrochloride Injection, Bedford, 074524, Calypsol, Ketalin, Ketamax, Ketanest, Ketava, Ketmin, Ketolar, Petar, Soon-Soon
Intervention Description
Separate dosing regimens will be applied depending on the weight of the child. Group A with minimum-maximum weight of 20 kg-40 kg will receive a fixed initial dose of 10 mg ketamine(0.25-0.5mg/kg)and will not exceed a maximum dose of 40 mg ketamine. Group B with minimum - maximum weight of 40.01kg-100kg will get a fixed initial dose of 20 mg ketamine(0.20-0.5mg/kg) and will not exceed a maximum dose of 120mg. ketamine. There will be 4 administrations of the drug at three day intervals. Titration upward will depend upon degree of side effects, improvement from baseline on primary measures, subjective opinion. Doses will be held constant as long as a therapuetic response, as measure of 80% improvement on YBOCS and YMRS, is reached.
Intervention Type
Drug
Intervention Name(s)
Flat tonic water (e.g., Canada Dry Tonic Water)
Intervention Description
Separate dosing regimens will be applied depending on the weight of the child. Group A with minimum-maximum weight of 20 kg-40 kg will receive a fixed initial dose of 0.1cc placebo and not exceed a maximum dose of 0.4cc placebo. Group B with minimum - maximum weight of 40.01kg-100kg will get a fixed initial dose of 0.2cc placebo and will not exceed a maximum dose of 1.2cc. placebo. There will be 4 administrations of the placebo at three day intervals. Titration upward will depend upon degree of side effects, improvement from baseline on primary measures, and subjective opinion. Doses will be held constant as long as a therapuetic response, as a measure of 80% improvement on YBOCS and YMRS, is reached.
Primary Outcome Measure Information:
Title
Young Mania Rating Scale
Time Frame
Change from baseline at 8 days
Title
Young Mania Rating Scale
Time Frame
Change from baseline at 11 days
Title
Young Mania Rating Scale
Time Frame
Change from baseline at 14 days
Title
Young Mania Rating Scale
Time Frame
Change from baseline at 17 days
Title
Overt Aggression Scale
Time Frame
Change from baseline at day 8
Title
Overt Aggression Scale
Time Frame
Change from baseline at day 11
Title
Overt Aggression Scale
Time Frame
Change from baseline at day 14
Title
Overt Aggression Scale
Time Frame
Change from baseline at day 17
Title
Yale Brown Obsessive Compulsive Scale
Time Frame
Change from baseline at Day 18, aggressive and obsessive questions
Secondary Outcome Measure Information:
Title
Wechsler Intelligence Scale for Children-IV
Time Frame
Change from baseline at day 18
Title
Peripheral Thermal Challenge
Time Frame
Change from baseline on days 6, 7, 15 and 16
Title
body temperature
Description
A proprietary ambulatory monitor will measure skin and tympanic temperature using conventional thermistors and IR sensors
Time Frame
Change from baseline over 16 hours spanning days 6-7 and 15-16.
Title
Triaxial acceleration
Description
A proprietary ambulatory monitor will measure triaxial acceleration from the forehead using a commercially-available sensor that also provides a plethysmograph signal from which heart rate can be derived.
Time Frame
Change from baseline over 16 hours spanning days 6-7 and 15-16.
Title
SpO2
Description
A proprietary ambulatory monitor will measure triaxial acceleration from the forehead using a commercially-available sensor that also provides a plethysmograph signal from which heart rate can be derived.
Time Frame
Change from baseline over 16 hours spanning days 6-7 and 15-16.
Title
Galvanic skin response
Description
A proprietary ambulatory monitor will measure galvanic skin response obtained with two conventional electrodes.
Time Frame
Change from baseline over 16 hours spanning days 6-7 and 15-16.
Title
Delis-Kaplin Executive Function System
Time Frame
Change from baseline on day 18
Title
Conner's Continuous Performance Test
Time Frame
Change from baseline on day 18
Title
SCARED
Time Frame
change from baseline at day 18
10. Eligibility
Sex
All
Minimum Age & Unit of Time
6 Years
Maximum Age & Unit of Time
12 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Males and females aged 6-12;
DSM-IV bipolar disorder (BPI, BPII, BP-NOS, BP-FOH);
Treatment resistant - as defined by failure to adequately respond to at least 2 different classes of medications such as mood stabilizers and antipsychotic agent.
Exclusion Criteria:
Contraindication to the use of ketamine, including allergy and current use of medicine contraindicated with ketamine;
Endocrine or neurological illness;
Previous history of closed head injury, current head injury associated with possible intracranial hypertension, central nervous system masses, abnormalities, or hydrocephalus, ever had loss of consciousness;
Previous history of glaucoma or acute globe injury
Abnormal nasal physiology which would not allow for adequate medication delivery;
Any change in medication type or dose within the past 30 days;
Treatment with any MAOI's currently or within the past 3 months;
Has had a course of ECT within the past 3 months;
Has ever used PCP or ketamine;
Meets DSM-IV criteria for Mental Retardation;
Has ever had Repetitive Transcranial Magnetic Stimulation (rTMS), Vagal Nerve Stimulation (VNS) or Deep Brain Stimulation;
Is currently hospitalized;
Has known or suspected schizophrenia, even if currently stable or controlled with medications
Is acutely suicidal or homicidal (i.e., in imminent danger with plan, urges and intent to harm oneself or others) including any serious attempts/those requiring hospitalization in the past 12 months or at the PI's discretion;
The presence of any abnormal laboratory findings or serious medical disorder or condition including: clinically significant organ system dysfunction; significant endocrine disease, including diabetes mellitus; hypothyroidism; cardiovascular disease (myocardial ischemia, heart failure, arrhythmias); coagulopathy; significant anemia; significant acute infection; glaucoma; dehydration; epilepsy; any intra-abdominal or intrathoracic surgery or limb amputation within the prior 6 months; any diagnosed cardiac condition causing documented hemodynamic compromise or dysfunction of the SA or AV node; any diagnosed respiratory condition causing documented or clinically recognized hypoxia (e.g., chronic obstructive or restrictive pulmonary disease); body weight approximately < 80% or > 120% ideal body weight; or any medical condition known to interfere with cognitive performance; medication-related exclusions include narcotic therapy, chronic acetaminophen use, acute sedative hypnotic withdrawal, corticosteroid or spironolactone therapy, regularly dosed narcotics or any other sedative therapy or medication that interferes with SA or AV node function or could be considered contraindicated with the sedative properties of ketamine.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Demitri Papolos, MD
Organizational Affiliation
Juvenile Bipolar Research Foundation
Official's Role
Principal Investigator
Facility Information:
Facility Name
Individual homes of subjects
City
Not Predetermined
State/Province
Connecticut
Country
United States
Facility Name
Juvenile Bipolar Research Foundation
City
Maplewood
State/Province
New Jersey
ZIP/Postal Code
07040
Country
United States
Facility Name
Individual homes of subjects
City
Not Predetermined
State/Province
New Jersey
Country
United States
Facility Name
Individual homes of subjects
City
Not Predetermined
State/Province
New York
Country
United States
12. IPD Sharing Statement
Links:
URL
http://www.jbrf.org/
Description
Juvenile Bipolar Research Foundation
URL
http://www.jbrf.org/librarydocs/correctedproof-7-23-09.pdf
Description
Fear of harm, a possible phenotype of pediatric bipolar disorder
URL
http://www.jbrf.org/cpp/index.html
Description
Diagnostic Assessment Program for Juvenile Bipolar Disorder
URL
http://www.jbrf.org/librarydocs/JADPhenotypeArticle.pdf
Description
A strategy for identifying phenotypic subtypes
Learn more about this trial
Intranasal Ketamine In the Treatment of Pediatric Bipolar Disorder
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