Status:
TERMINATED
Intranasal Ketamine In the Treatment of Pediatric Bipolar Disorder
Lead Sponsor:
Juvenile Bipolar Research Foundation
Conditions:
Bipolar Disorder
Eligibility:
All Genders
6-12 years
Phase:
PHASE2
PHASE3
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...
Eligibility Criteria
Inclusion
- 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
- 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.
Key Trial Info
Start Date :
July 1 2012
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
November 1 2016
Estimated Enrollment :
5 Patients enrolled
Trial Details
Trial ID
NCT01504659
Start Date
July 1 2012
End Date
November 1 2016
Last Update
March 16 2017
Active Locations (4)
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1
Individual homes of subjects
Not Predetermined, Connecticut, United States
2
Juvenile Bipolar Research Foundation
Maplewood, New Jersey, United States, 07040
3
Individual homes of subjects
Not Predetermined, New Jersey, United States
4
Individual homes of subjects
Not Predetermined, New York, United States