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临床试验/NCT04599504
NCT04599504已完成2 期

Pharmacological and Behavioral Treatments to Treat Loss-of-Control Eating and Improve Weight Outcomes After Bariatric Surgery: Medication Change for Non-Responders (Stage 2b)

Yale University1 个研究点 分布在 1 个国家目标入组 16 人开始时间: 2022年1月2日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
16
试验地点
1
主要终点
Loss-of-Control Eating Frequency

研究概览

简要总结

This study will test the effectiveness of lisdexamfetamine medication as a treatment for loss-of-control eating and weight following bariatric surgery. This is a controlled test of whether, amongst non-responders to acute treatments, lisdexamfetamine medication results in superior outcomes compared with placebo.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 64 Years(Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Be in the age range ≥18 years of age and <65 years of age.
  • •Have had laparoscopic Roux-en-Y gastric bypass or sleeve gastrectomy
  • •Approximately ten months post-surgery
  • •Experienced regular loss of control eating about six months after bariatric surgery, and were considered treatment non-responders to a four-month treatment trial of medication and/or BWL
  • •Be an otherwise healthy subject without uncontrolled medical problems, as determined by the study physician and medical co-investigators (physical examination, laboratory studies).
  • •Read, comprehend, and write English at a sufficient level to complete study-related materials.
  • •Provide a signed and dated written informed consent prior to study participation.
  • •Be available for participation in the study for up to 15 months (3-month treatment plus 12-month follow up).

排除标准

  • •Has a predisposition to seizures (e.g., subject with a history or evidence of seizure disorder, febrile seizures during childhood, brain tumor, cerebrovascular disease, or significant head trauma; has a family history of idiopathic seizure disorder or is currently being treated with medications or treatment regimens that lower seizure threshold).
  • •Has a history of anorexia nervosa or history of bulimia nervosa.
  • •Is currently using other medications for weight loss.
  • •Has a co-existing psychiatric condition that requires hospitalization or more intensive treatment (such as bipolar mood disorders, psychotic illnesses, or severe depression)
  • •Has untreated hypertension with a seated systolic blood pressure > 160 mmHg, diastolic blood pressure > 100 mmHg, or heart rate > 100 beats/minute.
  • •Has a history of congenital heart disease, cardiovascular disease, cardiac arrhythmias requiring medication, or a history of cerebrovascular pathology including stroke.
  • •Has current uncontrolled hypertension.
  • •Has current uncontrolled Type I or Type II diabetes mellitus.
  • •Has untreated hypothyroidism with a TSH > 1.5 times the upper limit of normal for the test laboratory with repeat value that also exceeds this limit.
  • •Has gallbladder disease.
  • •Has a history of severe renal, hepatic, neurological, chronic pulmonary disease, or any other unstable medical disorder.
  • •Is currently in active treatment for eating or weight loss.
  • •Is currently participating in another clinical study in which the subject is or will be exposed to an investigational or a non-investigational drug or device.
  • •Is breast-feeding or is pregnant or is not using a reliable form of birth control.
  • •Reports active suicidal or homicidal ideation.
  • •Previous history of problems with LDX or other stimulants.
  • •Has a history of allergy or sensitivity to LDX or other stimulant medications.
  • •Current medication contraindicated with study medication.
  • •Any current psychostimulant use or any medication for ADHD.
  • •History or current alcohol or substance use disorder (smoking will not be exclusionary)
  • •Is currently taking MAOI medication, SSRI medication, or strong inhibitors of CYP2D6

研究组 & 干预措施

Placebo

Placebo Comparator

干预措施: Placebo (Other)

Lisdexamfetamine dimesylate

Experimental

干预措施: Lisdexamfetamine Dimesylate (Medication) (Drug)

结局指标

主要结局

Loss-of-Control Eating Frequency

时间窗: At the end of 12-week treatment

Loss-of-control eating frequency is a continuous variable of loss-of-control eating episodes assessed using the Eating Disorder Examination interview; Loss-of-control eating frequency will be based on the past 28 days and defined as loss-of-control eating episodes per month.

Loss-of-Control Eating Frequency

时间窗: 6-month follow-up from the end of treatment

Loss-of-control eating frequency is a continuous variable of loss-of-control eating episodes assessed using the Eating Disorder Examination interview; Loss-of-control eating frequency will be based on the past 28 days and defined as loss-of-control eating episodes per month.

Loss-of-Control Eating Frequency

时间窗: 12-month follow-up from the end of treatment

Loss-of-control eating frequency is a continuous variable of loss-of-control eating episodes assessed using the Eating Disorder Examination interview; Loss-of-control eating frequency will be based on the past 28 days and defined as loss-of-control eating episodes per month.

Percent Weight Change

时间窗: From baseline at study enrollment to after the 12-week treatment

Percent weight loss is calculated based on change from pre-treatment to post-treatment at 3 months. Negative values indicate weight loss.

Percent Weight Change

时间窗: From post-treatment to the 6-month follow-up

Percent weight loss is calculated based on change from post-treatment to the 6-month follow-up. Negative values indicate weight loss.

Percent Weight Change

时间窗: From post-treatment to the 12-month follow-up

Percent weight loss is calculated based on change from post-treatment to the 12-month follow-up. Negative values indicate weight loss.

次要结局

未报告次要终点

研究者

发起方
Yale University
申办方类型
Other
责任方
Sponsor

研究点 (1)

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