Naltrexone
Drug3 tablets(15mg) once per day in the first two weeks,then Naltrexone 5 tablets(25mg) once per day during the rest of the study.
NCT Number: NCT02736474
The purpose of this research is to observe the efficacy of Naltrexone and Bupropion combination on weight loss and smoking cessation from baseline to week 24 compare to placebo.
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Notify Me18 year–65 year
All sexes
Interventional
Phase 4
This is a randomized, double-blind, and placebo-controlled study. Subjects with evaluation and confirmation that inclusion and exclusion criteria are met, will be treated with naltrexone sustained release 15mg once per day and bupropion sustained release 150mg once per day in the first two weeks, and naltrexone 25mg once per day and bupropion 300mg once per day during the rest of the study.The purpose of this research is to observe the efficacy of Naltrexone and Bupropion on weight loss and smoking cessation compared to placebo.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
3 tablets(15mg) once per day in the first two weeks,then Naltrexone 5 tablets(25mg) once per day during the rest of the study.
Placebo Naltrexone created and masked by the pharmacy to be used as a control.
1 capsule(150mg) once per day in the first two weeks,then 2 capsules(300mg) once per day during the rest of the study.
Placebo Bupropion created and masked by the pharmacy to be used as a control.
Time frame: baseline and 24 weeks
evaluate all participants' weight ,weight in kilograms
Time frame: 24 weeks
Time frame: baseline and 24 weeks
The visual analogue scale is a scale that is used to gauge smoking craving. Patients can choose a number from 0 to 10 to show their smoking craving, in which "0" represents "no craving" and "10" represents "intense urge".
Time frame: 24 weeks
evaluate all participants' depression status by Self-rating depression scale(SDS),which has a theoretical value range of 20-80. The SDS total score ranges, with the higher the score representing the higher level of severity of depression.
Time frame: 24 weeks
evaluate all participants' depression status by Self-Rating Anxiety Scale,which has a theoretical value range of 20-80. The SAS total score ranges, with the higher the score representing the higher level of severity of anxiety.
Time frame: 24 weeks
Through a simple 40 to 50 minute talk with the patient, the physician scored 30 different symptoms on a scale of 1-7 to get their PANSS score. The total score range from 30-210. The PANSS total score ranges, with the higher the score representing the higher level of severity of clinical symptoms.
Time frame: 24 weeks
evaluate all participants' waist circumference,waist circumference in centimeters
Time frame: baseline and 24 weeks
Time frame: baseline and 24 weeks
Time frame: baseline and 24 weeks
Time frame: baseline and 24 weeks
Time frame: baseline and 24 weeks
Time frame: baseline and 24 weeks
Time frame: baseline and 24 weeks
Time frame: baseline and 24 weeks
Shanghai Mental Health Center
Other
Effect of Naltrexone and Bupropion Combination on Weight Loss and Smoking Cessation in Obese, Cigarette-smoking Patients With Schizophrenia
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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