The purpose of this study is to determine whether lorcaserin is effective for weight reduction in patients with weight gain as a result of antipsychotic medications.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
15
Patients will receive lorcaserin 10mg tablet, 1 tablet twice daily for 12 weeks.
All patients in the study will receive intensive dietary counseling, encouraging eating minimal carbohydrates and sugars.
VA Long Beach
Long Beach, California, United States
RECRUITINGWeight loss
The primary objective of this study is to evaluate the effectiveness of lorcaserin for weight loss management in patients on an antipsychotic agent. Will monitor the weight of the patient for evaluation.
Time frame: initial visit with provider, then at weeks 1, 2, 4, 8, 12, and 16 of the study
Evaluation of glucose control
Will evaluate lab values for fasting blood glucose, Hemoglobin A1c, and fasting insulin levels
Time frame: At initial visit and at week 12 of the study
Evaluation of cravings
Using various questionnaires to evaluate cravings of various foods.
Time frame: initial visit with provider, then at weeks 1, 2, 4, 8, 12, and 16 of the study
Monitoring of mood
Using standard questionnaires to evaluate mental health.
Time frame: At initial visit, then at week 4 and week 12 of the study
Evaluation of systolic blood pressure
Time frame: initial visit with provider, then at weeks 1, 2, 4, 8, 12, and 16 of the study
Evaluation of diastolic blood pressure
Time frame: initial visit with provider, then at weeks 1, 2, 4, 8, 12, and 16 of the study
Evaluation of pulse
Time frame: initial visit with provider, then at weeks 1, 2, 4, 8, 12, and 16 of the study
Evaluation of body-mass index (BMI)
Time frame: initial visit with provider, then at weeks 1, 2, 4, 8, 12, and 16 of the study
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Evaluation of waist circumference
Time frame: initial visit with provider, then at weeks 1, 2, 4, 8, 12, and 16 of the study
Evaluation of cholesterol control
Will measure fasting cholesterol labs, which will include total cholesterol, triglycerides, low-density lipoprotein (LDL), and high-density lipoprotein (HDL)
Time frame: At initial visit and at week 12 of the study
Evaluation of electrolytes
Will monitor basic metabolic panel
Time frame: At initial visit and at week 12 of the study
Evaluation of liver
Will monitor liver enzymes
Time frame: At initial visit and at week 12 of the study
Evaluation of blood count
Will monitor blood count
Time frame: At initial visit and at week 12 of the study