Adjunct Phentermine + Topiramate After Bariatric Surgery in 12-24 Year Olds

Obesity, Morbid Clinical Trial

Official title:

Adjunctive Anti-Obesity Pharmacotherapy in Adolescents and Young Adults After Bariatric Surgery: A Randomized Controlled Pilot Study

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04095104
• Other study ID #: 18-2793
• Secondary ID: 5P30DK048520-24
• Status: Completed
• Phase: Phase 2
• Start date: January 15, 2020
• Est. completion date: January 25, 2022

Study information

• Verified date: March 2022
• Source: Children's Hospital Colorado
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The goal of this pilot study is to establish the feasibility and initial efficacy of the combination of phentermine and topiramate for adolescents and young adults who require additional risk reduction after bariatric surgery. This study will use a randomized, placebo-controlled, double-blinded design to evaluate an adjunctive 12-week intervention of phentermine + topiramate + standard of care vs. placebos + standard of care 6 months after bariatric surgery, among 12 to 24 year olds who don't achieve expected weight loss or who remain severely obese (n=10 total).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 13
• Est. completion date: January 25, 2022
• Est. primary completion date: January 25, 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: 12 Years to 24 Years

Eligibility

Inclusion Criteria:

• Status post sleeve gastrectomy or roux-en-y gastric bypass
• At 6 months after bariatric surgery, has not achieved >= 26% decrease in weight from preoperative weight (within 1 week of surgery) OR remains severely obese (>=120% of 95th%ile or BMI >=35kg/m2 for 12-17yo; BMI >=35kg/m2 for 18-24yo)

Exclusion Criteria:

• Absolute contraindication to phentermine or topiramate (i.e. phentermine:

history of coronary artery disease, stroke, arrhythmia, congestive heart failure, uncontrolled hypertension), hypersensitivity to sympathomimetic amines, current or recent (within 14 days) use of monoamine oxidase inhibitors, glaucoma, or hyperthyroidism; topiramate: hypersensitivity to topiramate, history of nephrolithiasis)

• Concomitant use of phenytoin, carbamazepine, or carbonic anhydrase inhibitors (e.g. zonisamide, acetazolamide, or dichlorphenamide)
• Use of anti-obesity medication within 6 months of screening
• Initiation of a new medication associated with weight loss or gain within 30 days of screening
• Type 2 diabetes mellitus
• Hypothalamic obesity
• Unmanaged (e.g. without medications and/or psychotherapy) clinically significant (determined by a mental health professional using diagnostic instruments and/or clinical interview) depression or anxiety
• History of any suicidal behavior within 30 days of screening or any suicidal ideation with either some intent to act or with intent and a specific plan within 30 days of screening
• History of schizophrenia
• Severe hepatic impairment (ALT >10x upper limit of normal or known synthetic liver dysfunction)
• Moderate or severe renal impairment (GFR <30mL/min/1.73m2)
• Dosage change to hypertension, dyslipidemia, depression, or anxiety medication <4 weeks prior to study enrollment
• Contraception started <7 days prior to study enrollment
• Current pregnancy/plans to become pregnant within 16 weeks from study drug start date
• Females without a long acting reversible contraceptive (LARC) who do not commit to using 2 forms of birth control

Related Conditions & MeSH terms

• Adolescent
• Bariatric Surgery
• Drug Therapy
• Obesity
• Obesity, Morbid
• Young Adult

Intervention

Drug:
• Phentermine
Phentermine tablet
• Immediate Release Topiramate
Topiramate tablet
• Placebo for Phentermine
Compounded tablet to mimic phentermine 8mg tablet
• Placebo for Immediate Release Topiramate
Compounded tablet to mimic immediate release topiramate 25mg tablet

Locations

Country	Name	City	State
United States	Children's Hospital Colorado	Aurora	Colorado

Sponsors (4)

Lead Sponsor	Collaborator
Jaime Moore, MD MPH	National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), University of Colorado- Clinical and Translational Sciences Institute, University of Colorado- Nutrition Obesity Research Center

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Enrollment Rate	Number enrolled divided by number eligible	24 months
Primary	Dropout Rate	Number who do not complete the study divided by number enrolled	24 months
Primary	Adherence to Study Drugs	Percentage of missed doses (pill count); Presence/Absence of amphetamine in the urine	12 weeks
Primary	Frequency of drug-related adverse events	Count and description of adverse events possibly or definitely related to the study drugs. Elicited using a standardized checklist during 3 study phone calls and 3 in-person study visits, laboratory monitoring of serum bicarbonate, and comprehensive review of systems, vitals, physical exam, and mood/suicidality assessment using validated instruments at every study visit.	24 months
Secondary	Percent weight change	(Baseline weight - Weight at 12 weeks)/Baseline weight x 100	Baseline and 12 weeks
Secondary	Percent BMI change	(Baseline BMI - BMI at 12 weeks)/Baseline BMI x 100	Baseline and 12 weeks
Secondary	Change in BMI percent of the 95th%ile	(Baseline BMI % of the 95th%ile - BMI % of the 95th%ile at 12 weeks)	Baseline and 12 weeks
Secondary	Change in heart rate	(Heart rate at baseline - Heart rate at 12 weeks)	Baseline and 12 weeks
Secondary	Change in systolic blood pressure	Systolic blood pressure at baseline - Systolic blood pressure at 12 weeks	Baseline and 12 weeks
Secondary	Change in diastolic blood pressure	Diastolic blood pressure at baseline - Diastolic blood pressure at 12 weeks	Baseline and 12 weeks
Secondary	Change in total cholesterol (mg/dL)	Total cholesterol at baseline - Total cholesterol at 12 weeks	Baseline and 12 weeks
Secondary	Change in triglycerides (mg/dL)	Triglycerides at baseline - Triglycerides at 12 weeks	Baseline and 12 weeks
Secondary	Change in LDL cholesterol (mg/dL)	LDL at baseline - LDL at 12 weeks	Baseline and 12 weeks
Secondary	Change in HDL cholesterol (mg/dL)	HDL at baseline - HDL at 12 weeks	Baseline and 12 weeks
Secondary	Change in alanine aminotransferase (ALT) (U/L)	ALT at baseline - ALT at 12 weeks	Baseline and 12 weeks
Secondary	Change in hemoglobin A1c (HbA1c) (%)	HbA1c at baseline - HbA1c at 12 weeks	Baseline and 12 weeks
Secondary	Change in % fat mass	% Fat mass at baseline - %Fat mass at 12 weeks measured by DEXA	Baseline and 12 weeks
Secondary	Change in resting metabolic rate (RMR)	RMR at baseline - RMR at 12 weeks measured by indirect calorimetry	Baseline and 12 weeks
Secondary	Change in Dietary Intake	The adolescent/young adult will complete a dietary record on 3 consecutive days (2 weekdays, 1 weekend day) based on standardized protocols for dietary assessment. Total caloric intake, macronutrient, and micronutrient breakdown will be assessed.	Baseline and 12 weeks
Secondary	Change in Hunger	The adolescent/young adult will report hunger before each meal and snack for 24 hours using a 100mm visual analogue scale (0= no hunger, 100 = most hunger)	Baseline and 12 weeks
Secondary	Change in Satiety	The adolescent/young adult will report satiety before each meal and snack for 24 hours using a 100mm visual analogue scale (0= no fullness, 100= most full)	Baseline and 12 weeks
Secondary	Change in Eating in the Absence of Hunger	Validated questionnaire: Eating in the Absence of Hunger-Parent (EAH-P) completed by the parent/guardian about their adolescent/young adult. This measure has 14 items.; Each item is on a 5-point Likert scale ranging from 1= "never" to 5= "always". A higher score indicates more eating in the absence of hunger.; Total and sub scales are calculated by taking the average of the items. Total score measures the overall construct "Eating in the Absence of Hunger" Subscales include: "External Cues" (4 items); "Response to negative affect" (6 items); "Fatigue/Boredom" (4 items).	Baseline and 12 weeks
Secondary	Change in Cognitive Restraint, Disinhibited Eating, and Predisposition to Hunger	The "Three-Factor Eating Questionnaire" will be completed by the adolescent/young adult. This is a 51-item measure that is divided into 2 parts, and assesses 3 eating behaviors: 1) Cognitive Dietary Restraint (20 items), 2) Disinhibited Eating (16 items), and 3) Predisposition to hunger (15 items). Higher scores in each domain indicate more of each of those behaviors.; The minimum score for factors 1, 2, and 3 are: 0, 0, and 0. The maximum score for factors 1, 2, and 3 are: 20, 16, and 15 Part I includes items 1-36 rated as either True (1) or False (0) Part II includes items 37-51 and is rated on a 4-point Likert-like scale with one exception- item 50 is rated on a 6-point scale.; Scores for each of the three eating behaviors are calculated by taking the average of the items, and are most commonly reported separately, not as a total score.	Baseline and 12 weeks
Secondary	Change in Weight Related Quality of Life- Adolescent	"Impact of Weight on Quality of Life-Kids" questionnaire will be completed by the adolescents age <=19.; Total and each of the 4 sub scales (Physical Comfort-6 items, Body Esteem-9 items, Social Life-6 items, and Family Relations-6 items) range from a minimum score of 0 to a maximum of 100.; Higher scores indicate higher quality of life.	Baseline and 12 weeks
Secondary	Change in Weight Related Quality of Life- Parent	"Impact of Weight on Quality of Life-Kids Parent Proxy" questionnaire will be completed by the parent of the adolescent/young adult.; Total and each of the 4 sub scales (Physical Comfort-6 items, Body Esteem-9 items, Social Life-6 items, and Family Relations-6 items) range from a minimum score of 0 to a maximum of 100.; Higher scores indicate higher quality of life.	Baseline and 12 weeks
Secondary	Change in Weight Related Quality of Life- Young adult	"Impact of Weight on Quality of Life-Lite" questionnaire will be completed by the young adult age >=20.; Total and each of the 5 sub scales (Physical function-11 items, Self Esteem-7 items, Sexual Life-4 items, Public distress-5 items, and Work-4 items) range from a minimum score of 0 to a maximum of 100.; Higher scores indicate higher quality of life.	Baseline and 12 weeks
Secondary	Change in General Health Related Quality of Life: PedsQL instrument	PedsQL instrument will be completed by the adolescent/young adult. There are 4 scales: Physical Functioning (8 items), Emotional Functioning (5 items), Social Functioning (5 items), and School Functioning (5 items) and 3 Summary Scores: Total Scale Score (23 items), Physical Health Summary Score (8 items), and Psychosocial Health Summary Score (15 items).; Items are rated on a 0-4 scale. Items are reverse scored and linearly transformed to a 0-100 scale, such that 0=100, 1=75, 2=50, 3=25, and 4=0.; Higher scores indicated better health-related quality of life. Scale Scores are calculated as the sum of the items over the number of items answered.; Psychosocial Health Summary Score is calculated as the sum of the items over the number of items answered in the Emotional, Social, and School Functioning Scales.; Physical Health Summary Score is the same as the Physical Functioning Scale Score.	Baseline and 12 weeks
Secondary	Change in Depression	The adolescent/young adult will complete the 20-item Center for Epidemiologic Studies Depression Scale (CES-D).; Each item is rated on a 0 to 3 scale (positive items are reverse scored). Minimum score is 0 and maximum is 60. Higher scores indicate more depressive symptoms. Total score is calculated by summing each of the 20 individual items scores.	Baseline and 12 weeks
Secondary	Participant Satisfaction: questionnaire	The participating family will be asked to complete a satisfaction questionnaire that will assess reasons for participation, experience during study visits, satisfaction with the effect of the study drug, ease of communication with study staff, and study burden.	At 12 weeks