Not provided
Not provided
Not provided
Not provided
Administrative issues
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
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.
Not provided
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Bipolar-Ketalar | Active Comparator | Children with a diagnosis of BP-I, BP-II or BP-NOS will receive 4 administrations of intranasal ketalar |
|
| Bipolar-Placebo | Placebo Comparator | Children with a diagnosis of BP-I, BP-II or BP-NOS will receive 4 administrations of placebo |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Ketamine hydrochloride injection | Drug | 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. |
| Measure | Description | Time Frame |
|---|---|---|
| Young Mania Rating Scale | Change from baseline at 8 days | |
| Young Mania Rating Scale | Change from baseline at 11 days | |
| Young Mania Rating Scale | Change from baseline at 14 days | |
| Young Mania Rating Scale | Change from baseline at 17 days | |
| Overt Aggression Scale | Change from baseline at day 8 | |
| Overt Aggression Scale | Change from baseline at day 11 | |
| Overt Aggression Scale | Change from baseline at day 14 | |
| Overt Aggression Scale | Change from baseline at day 17 | |
| Yale Brown Obsessive Compulsive Scale | Change from baseline at Day 18, aggressive and obsessive questions |
| Measure | Description | Time Frame |
|---|---|---|
| Wechsler Intelligence Scale for Children-IV | Change from baseline at day 18 | |
| Peripheral Thermal Challenge | Change from baseline on days 6, 7, 15 and 16 | |
| body temperature |
Not provided
Inclusion Criteria:
Exclusion Criteria:
Not provided
Not provided
Not provided
Not provided
Not provided
| Name | Affiliation | Role |
|---|---|---|
| Demitri Papolos, MD | Juvenile Bipolar Research Foundation | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Individual homes of subjects | Not Predetermined | Connecticut | United States | |||
| Juvenile Bipolar Research Foundation |
Not provided
| Label | URL |
|---|---|
| Juvenile Bipolar Research Foundation | View source |
| Fear of harm, a possible phenotype of pediatric bipolar disorder | View source |
| Diagnostic Assessment Program for Juvenile Bipolar Disorder |
Not provided
Not provided
| ID | Term |
|---|---|
| D001714 | Bipolar Disorder |
| D003863 | Depression |
| ID | Term |
|---|---|
| D000068105 | Bipolar and Related Disorders |
| D019964 | Mood Disorders |
| D001523 | Mental Disorders |
| D001526 | Behavioral Symptoms |
Not provided
Not provided
| ID | Term |
|---|---|
| D007649 | Ketamine |
| ID | Term |
|---|---|
| D003510 | Cyclohexanes |
| D003516 | Cycloparaffins |
| D006840 | Hydrocarbons, Alicyclic |
| D006844 | Hydrocarbons, Cyclic |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
|
|
| Flat tonic water (e.g., Canada Dry Tonic Water) | Drug | 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. |
|
A proprietary ambulatory monitor will measure skin and tympanic temperature using conventional thermistors and IR sensors |
| Change from baseline over 16 hours spanning days 6-7 and 15-16. |
| 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. | Change from baseline over 16 hours spanning days 6-7 and 15-16. |
| 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. | Change from baseline over 16 hours spanning days 6-7 and 15-16. |
| Galvanic skin response | A proprietary ambulatory monitor will measure galvanic skin response obtained with two conventional electrodes. | Change from baseline over 16 hours spanning days 6-7 and 15-16. |
| Delis-Kaplin Executive Function System | Change from baseline on day 18 |
| Conner's Continuous Performance Test | Change from baseline on day 18 |
| SCARED | change from baseline at day 18 |
| Maplewood |
| New Jersey |
| 07040 |
| United States |
| Individual homes of subjects | Not Predetermined | New Jersey | United States |
| Individual homes of subjects | Not Predetermined | New York | United States |
| A strategy for identifying phenotypic subtypes | View source |
| D001519 |
| Behavior |
| D006838 |
| Hydrocarbons |
| D009930 | Organic Chemicals |