Deep Brain Stimulation for Morbid Obesity

Obesity Clinical Trial

Official title:

Deep Brain Stimulation for the Treatment of Refractory Morbid Obesity

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03650309
• Other study ID #: 17-5899
• Status: Completed
• Phase: N/A
• Start date: September 1, 2018
• Est. completion date: July 23, 2022

Study information

• Verified date: May 2024
• Source: University Health Network, Toronto
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is an open-label, phase I pilot trial designed to evaluate the safety and feasibility of deep brain stimulation (DBS) for the treatment of refractory morbid obesity. Patients with diagnoses of morbid obesity will be recruited and enrolled. All patients will receive DBS targeting two brains areas involved in the pathophysiology of obesity and will be followed post-operatively for 12 months.

Description:

This study will establish 1)the safety of deep brain stimulation (DBS) in a patient population with treatment refractory morbid obesity. DBS has been used safely and effectively in thousands of patients for numerous disorders. Recent evidence (outlined above) has shown that DBS can also be used to manage refractory psychiatric conditions, such as depression and obsessive-compulsive disorder, as well as in eating disorders such as anorexia nervosa. Such studies indicate that a targeted therapy informed by the neuroanatomic and circuitry literature can be effective in altering pathological mood and behaviour. 2) evaluate the effectiveness of the procedure, which will be evaluated by the actual weight loss and resolution of the core symptoms of morbid obesity, including BMI, as well of, depression, self-esteem, and binge eating scores surrounding with loss or weight gain.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 6
• Est. completion date: July 23, 2022
• Est. primary completion date: January 23, 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: 20 Years to 70 Years

Eligibility

Inclusion Criteria:

1. Female or Male patients between age 20-60

2. Diagnosis of Morbid Obesity (defined as a BMI>40kg/m2 or BMI>35 with 1 obesity related comorbidity) OR a diagnosis of Binge Eating Disorder not responsive to recommended treatments (as defined by the DSM-5)

3. Failure or non eligibility of bariatric surgery with <50% of excess weight loss, with or without BMI>35 kg/m2, at 18 months or more after the operation; OR diagnosis of binge eating disorder for over 18 months

4. Diagnosis of food dependence via Yale Food Addiction Scale (YFAS) criteria

5. Normal neurological exam

6. Normal head CT scan and cerebral MRI

7. Patient informed and able to give written consent

8. Able to comply with all testing, follow-ups and study appointments and protocols

Exclusion Criteria:

1. Active neurologic disease such as epilepsy

2. Alcohol or substance dependence or abuse in the last 6 months, excluding caffeine and nicotine

3. Any contraindication to magnetic resonance imaging (MRI) or positron emission tomography (PET) scanning

4. Likely to relocate or move during the study's one year duration

5. Presence of cardiac arrhythmias, or other cardiac, respiratory, renal or endocrine conditions as a result of morbid obesity, that will result in significant risk from a surgical procedure.

6. Presence of epilepsy, stroke or degenerative disorder of the nervous system

7. Pregnancy

Related Conditions & MeSH terms

• Obesity
• Obesity, Morbid

Intervention

Device:
• Deep Brain Stimulation
All patients will undergo surgical implantation of a deep brain stimulation (DBS) system, which involves placement of stimulating electrodes in the brain. These electrodes will be used to deliver electrical current to target two brain structures involved in the pathophysiology of obesity.

Locations

Country	Name	City	State
Canada	Toronto Western Hospital, University Health Network	Toronto	Ontario

Sponsors (1)

Lead Sponsor	Collaborator
University Health Network, Toronto

Country where clinical trial is conducted

Canada, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Incidence of Treatment-Emergent Adverse Events	Patients will be closely monitored for adverse events following DBS surgery with regular check-ups.	12 months
Secondary	Weight	Weight (in kilograms) will be frequently assessed prior to and following DBS surgery.	12 months
Secondary	'Quality of Life Scale' Questionnaire	Patients will regularly complete the 16-item Quality of Life Scale questionnaire (worst score = 16, best score = 112) to assess psychosocial function.	12 months
Secondary	'Behavioral Inhibition System/Behavioral Activation System Scales (BIS/BAS Scales)' Questionnaire	Patients will regularly complete the 24-item BIS/BAS Scales questionnaire to assess psychosocial behaviour. This questionnaire has 3 sub-scales: 'BAS drive' (highest score = 16, lowest score = 4), 'BAS fun seeking' (highest score = 20, lowest score = 5), 'BAS reward responsiveness' (highest score = 20, lowest score = 5), and 'BIS' (highest score = 28, lowest score = 7).	12 months
Secondary	'Patient Health Questionnaire (PHQ-9)' Questionnaire	Patients will regularly complete the 9-item PHQ-9 questionnaire (worst score = 27, best score = 0) to assess mood and depression symptoms.	12 months
Secondary	'Generalized Anxiety Disorder 7-item (GAD-7)' Questionnaire	Patients will regularly complete the 7-item GAD-7 questionnaire (worst score = 21, best score = 0) to assess anxiety symptoms.	12 months
Secondary	'Difficulties in Emotion Regulation Scale (DERS)' Questionnaire	Patients will regularly complete the 36-item DERS questionnaire (worst score = 180, best score = 36) to assess emotional dysregulation.	12 months
Secondary	'Yale-Brown Obsessive Compulsive Scale (Y-BOCS)' Questionnaire	Patients will regularly complete the 10-item Y-BOCS questionnaire (worst score = 40, best score = 0) to assess severity of obsessive and compulsive symptoms	12 months
Secondary	'Binge Eating Scale (BES)' Questionnaire	Patients will regularly complete the 16-item BES questionnaire (worst score = 43, best score = 0) to assess binge eating symptoms	12 months
Secondary	'Yale-Brown-Cornell Eating Disorder Scale (YBC-EDS)' Questionnaire	Patients will regularly complete the 19-item YBC-EDS questionnaire (worst score = 32, best score = 0) to assess eating-related preoccupations and rituals	12 months
Secondary	'Emotional Eating Scale (EES)' Questionnaire	Patients will regularly complete the 25-item EES questionnaire (worst score = 100, best score = 0) to assess their emotional relationship with food.	12 months
Secondary	'Power of Food (POF)' Questionnaire	Patients will regularly complete the 15-item POF questionnaire (worst score = 75, best score = 15) to assess the degree of influence food exerts on their day-to-day life.	12 months
Secondary	'Eating Disorder Examination Questionnaire (EDE-Q)'	Patients will regularly complete the 28-item EDE-Q (worst score = 6, best score = 0) to assess aspects of eating behaviour including restraint, eating concern, shape concern, and weight concern.	12 months
Secondary	'Yale Food Addiction Scale (YFAS)' Questionnaire	Patients will regularly complete the 25-item YFAS (higher numbers = more severe symptoms) to assess the severity of food addiction.	12 months