1/2-MC4R Genotype and Pediatric Antipsychotic Drug- Induced Weight Gain
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| ClinicalTrials.gov Identifier: NCT01844700 |
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Recruitment Status :
Terminated
(very slow recruitment, no sufficient results)
First Posted : May 1, 2013
Results First Posted : February 5, 2016
Last Update Posted : February 5, 2016
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| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| High Risk MC4R Genotype Low Risk MC4R Genotype One Week or Less Antipsychotic Lifetime Exposure | Drug: Ziprasidone Drug: aripiprazole, quetiapine, or risperidone | Phase 4 |
| Study Type : | Interventional (Clinical Trial) |
| Actual Enrollment : | 14 participants |
| Allocation: | Randomized |
| Intervention Model: | Parallel Assignment |
| Masking: | None (Open Label) |
| Official Title: | 1/2-MC4R Genotype and Pediatric Antipsychotic Drug- Induced Weight Gain |
| Study Start Date : | July 2013 |
| Actual Primary Completion Date : | April 2014 |
| Actual Study Completion Date : | April 2014 |
| Arm | Intervention/treatment |
|---|---|
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Active Comparator: Ziprasidone
(20-160mg/d, bid) for 12 weeks
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Drug: Ziprasidone
random assignment to ZIP (20-160mg/d, bid dosing)
Other Name: Geodon |
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Active Comparator: Aripiprazole, quetiapine, risperidone
Aripiprazole (2-30mg/d), Quetiapine (25-800mg/d) or Risperidone (0.1-8mg/d) for 12 weeks
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Drug: aripiprazole, quetiapine, or risperidone
random assignement to Usual Care antipsychotic UC antipsychotic (aripiprazole 2-30mg/d, quetiapine 25-800mg/d or risperidone 0.1-8mg/d)
Other Name: Abilify, Seroquel, Risperdal |
- Weight Change [ Time Frame: baseline to week 12 ]
- Percent Weight Change Compared to Baseline Weight [ Time Frame: baseline to week 12 ]
- BMI Z-scores [ Time Frame: baseline to week 12 ]
- BMI Percentile [ Time Frame: baseline to week 12 ]
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| Ages Eligible for Study: | 13 Years to 18 Years (Child, Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- age 13-18 years
- English-speaking
- DSM diagnoses that have an FDA indication for SGA use for at least one agent in the respective pediatric or adult age group. Specifically, primary DSM-IV diagnosis of early-onset schizophrenia spectrum disorders; bipolar I disorder mania (and BP-NOS); irritability associated with autism spectrum disorder, as well as severe mood dysregulation (SMD) according to Leibenluft et al. (2011) with an ABC-irritability score of >/=18 Sexually active girls must agree to use two effective forms of birth control or be abstinent
- Participant has a primary caretaker who has known the child well for at least 6 months before study entry Primary caretaker is able to participate in study appointments
- Ability of child to participate in all aspects of the protocol per investigator clinical judgment.
Exclusion Criteria:
- Major neurological or medical illnesses that affect weight (e.g., unstable thyroid disease), require a prohibited systemic medication (e.g., diabetes mellitus [insulin], chronic renal failure [steroids); Fasting glucose > 125 mg/dL on 2 occasions during screening
- Any medication (other than currently prescribed psychotropic medications) that would significantly alter weight
- Antidepressants not allowed for at least 2 weeks in BP-I or BP-NOS patients
- DSM-IV diagnosis of anorexia or bulimia nervosa
- DSM-IV diagnosis of Substance Dependence disorder (other than tobacco dependence) within the past month
- Initial urine toxicology screen and follow-up screen indicate ongoing use of illicit substance
- Hypersensitivity to ZIP or UC antipsychotics
- Pregnant, breast feeding or unwilling to comply with contraceptive requirements
- Screening or baseline QTc > 450 msec
- IQ < 55
- Significant risk for dangerousness to self or to others
- Ongoing or previously undisclosed child abuse requiring new department of social service intervention.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01844700
| United States, New York | |
| Zucker Hillside Hospital, Psychiatry Research | |
| Glen Oaks, New York, United States, 11004 | |
| Responsible Party: | Anil K. Malhotra, Director, Psychiatric Research, Northwell Health |
| ClinicalTrials.gov Identifier: | NCT01844700 |
| Other Study ID Numbers: |
12-403A |
| First Posted: | May 1, 2013 Key Record Dates |
| Results First Posted: | February 5, 2016 |
| Last Update Posted: | February 5, 2016 |
| Last Verified: | January 2016 |
|
MC4R genotype antipsychotic induced weight gain pediatric population |
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Weight Gain Body Weight Changes Body Weight Risperidone Quetiapine Fumarate Aripiprazole Ziprasidone Serotonin Antagonists Serotonin Agents Neurotransmitter Agents Molecular Mechanisms of Pharmacological Action Physiological Effects of Drugs |
Antipsychotic Agents Tranquilizing Agents Central Nervous System Depressants Psychotropic Drugs Dopamine Antagonists Dopamine Agents Antidepressive Agents Dopamine Agonists Serotonin 5-HT1 Receptor Agonists Serotonin Receptor Agonists Serotonin 5-HT2 Receptor Antagonists Dopamine D2 Receptor Antagonists |

