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Completed

NCT Number: NCT02736474

Naltrexone and Bupropion Combination on Obese,Smoking Patients With Schizophrenia

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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Key information

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • diagnosis of schizophrenia by the International Classification of Diseases 10th Revision (ICD-10);
  • age between 18 and 65 years old;
  • on stable antipsychotic medication treatment for at least one month;
  • BMI > 28 kg/m2 according to BMI criterion for obesity in the Chinese population , or BMI>27 kg/m2 in the presence of dyslipidemia, or male with waist circumference over 90cm;
  • smoking at least 10 cigarettes daily for one year or longer;
  • desire to lose weight and quit smoking.

Exclusion criteria

  • Binge eating or other eating disorders;
  • Current use of weight loss or antidiabetic medications;
  • Current substance use (except nicotine or caffeine);
  • Elevated hepatic transaminase levels (>2.5x normal range);
  • Clinically significant Thyroid Stimulating Hormone(TSH) and/or thyroxine4(T4) abnormalities;
  • History of seizure disorder;
  • History of unstable cardiac problems or other unstable medication conditions;
  • Being pregnant or nursing (for women).

Treatment and study plan

Naltrexone

Drug

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

Drug

Placebo Naltrexone created and masked by the pharmacy to be used as a control.

bupropion

Drug

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

Drug

Placebo Bupropion created and masked by the pharmacy to be used as a control.

Primary outcomes

  1. Change From Baseline in Weight at 24 Weeks

    Time frame: baseline and 24 weeks

    evaluate all participants' weight ,weight in kilograms

Secondary outcomes

  1. Numbers of Participants Who Quit Smoking

    Time frame: 24 weeks

  2. Changes From Baseline Craving for Nicotine Assessed by Visual Analog Scales (VAS) at 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".

  3. Depression Status Assessed by Self-rating Depression Scale(SDS)

    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.

  4. Anxiety Status Assessed by Self-Rating Anxiety Scale(SAS)

    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.

  5. Clinical Symptoms Assessed by the Positive and Negative Syndrome Scale (PANSS)

    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.

  6. Waist Circumference

    Time frame: 24 weeks

    evaluate all participants' waist circumference,waist circumference in centimeters

  7. Change in Fasting Blood Glucose Levels

    Time frame: baseline and 24 weeks

  8. Change in Fasting Insulin Levels

    Time frame: baseline and 24 weeks

  9. Change in Glycosylated Hemoglobin

    Time frame: baseline and 24 weeks

  10. Change in Fasting Triglycerides Levels

    Time frame: baseline and 24 weeks

  11. Change in Fasting HDL Cholesterol Levels

    Time frame: baseline and 24 weeks

  12. Change in Fasting LDL Cholesterol

    Time frame: baseline and 24 weeks

  13. Change in Leptin

    Time frame: baseline and 24 weeks

  14. Change in Ghrelin

    Time frame: baseline and 24 weeks

Sponsors and collaborators

Lead sponsor

Shanghai Mental Health Center

Other

Collaborators

  • University of Massachusetts, Worcester

Registry information

Official study title

Effect of Naltrexone and Bupropion Combination on Weight Loss and Smoking Cessation in Obese, Cigarette-smoking Patients With Schizophrenia

Important dates

Study start
2016
Primary completion
2018
Study completion
2018
First posted
Apr 13, 2016
Registry last updated
Oct 22, 2021

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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