Body Composition Changes With Albuterol and Caffeine Versus Placebo in Adolescents

NCT ID: NCT02740660

Last Updated: 2019-10-08

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 12 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2016-04-30
• Study Completion Date: 2017-10-31

Brief Summary

The purpose of this study is to determine whether taking a combination of caffeine and albuterol three times per day will increase muscle and decrease fat in your child's body and to determine how these medications make your child feel. Albuterol is approved by the FDA for the treatment of asthma. It is not approved to increase muscle and decrease body fat in children.

Detailed Description

Previous studies done at Pennington Biomedical have demonstrated that the equivalent of oral albuterol 4mg three times a day (tid) with oral caffeine 100mg tid reduces body fat and increases lean tissue in rodents more than the addition of the effect of the two components separately. The combination of albuterol with caffeine changed body composition without changing food intake. An adult male taking albuterol 4 mg orally tid plus caffeine 100mg orally tid increased lean mass by 1.25% and decreased fat mass by 1.2% over a two month period. These effects are expected to be even greater in a growing adolescent. This pilot project will take the first step towards trying to understanding the safety and potential efficacy of this drug combination. The prospect of using inexpensive medications already approved in the pediatric population for the treatment of asthma as a novel treatment for adolescent obesity addresses a medical need that is presently unmet.

Food restriction in adolescence is not only difficult to accomplish, but it also raises concerns about growth and development. A medication approved for the treatment of obesity in the adolescent age group that improves body composition by reducing body fat and increasing lean tissue without needing to restrict food intake would be a useful tool for physicians who address the treatment of obesity in adolescents. Albuterol is a medication, approved for ages 6 and older, used for the treatment of asthma and has also been shown to increase muscle strength and lean body mass in children with spinal muscular atrophy and in healthy young men during an exercise training program. A drug approved for the treatment of adolescent obesity that increases lean tissue, decreases fat tissue and can be given in conjunction with lifestyle modifications would be welcomed by both pediatricians who treat these adolescents and by adolescents who are stigmatized by their obesity.

A provisional patent has been submitted by Pennington Biomedical Research Center to protect the combination of caffeine and albuterol in a 1:25 ratio for synergistically increasing muscle mass and decreasing fat mass as a potential treatment for obesity in adolescents.

This study will be a double-blinded, randomized, placebo-controlled, pilot study in which subjects will be randomized to receive either placebo or a combination of Albuterol 4 mg and Caffeine 100mg three times per day orally for a total of 8 weeks. Each subject will continue on the study intervention for the entire duration of treatment

Conditions

Pediatric Obesity

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: TRIPLE

Study Groups

Caffeine 100mg / Albuterol 4mg

One capsule 3 times per day orally for a total of 8 weeks and family weight management counseling for a total of 8 weeks.

Group Type: EXPERIMENTAL

Caffeine 100mg / Albuterol 4mg

Intervention Type: DRUG

Family weight management counseling

Intervention Type: BEHAVIORAL

Placebo

One capsule 3 times per day orally for a total of 8 weeks and family weight management counseling for a total of 8 weeks.

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DRUG

Family weight management counseling

Intervention Type: BEHAVIORAL

Interventions

Caffeine 100mg / Albuterol 4mg

Intervention Type: DRUG

Placebo

Intervention Type: DRUG

Family weight management counseling

Intervention Type: BEHAVIORAL

Eligibility Criteria

Inclusion Criteria

• Healthy males or females with a BMI ≥ 95th percentile
• Between 12 and 17 years of age inclusive
• Tanner Stage III and above

Exclusion Criteria

• Weigh less than 50 kg
• Have a family history of sudden death or hypertrophic cardiomyopathy
• Have a history of unexplained syncope
• Have a marked baseline prolongation of QT/QTc interval (QTc interval >450 ms), a history of additional risk factors for torsade de pointes (e.g., heart failure, hypokalemia, family history of Long QT Syndrome), or use concomitant medications that prolong the QT/QTc interval
• Have history of asthma, hypertension, thyroid disease, or significant neurologic disease such as seizure disorder
• Are pregnant, planning to become pregnant, or nursing. Females who are sexually active must be using adequate contraception.
• Take a medication known to affect weight or body composition like systemic glucocorticoids, atypical anti-psychotics, or weight loss medications
• Take beta-stimulators or beta-blockers on a regular basis
• Take stimulants for attention deficit disorder
• Take monoamine oxidase inhibitors, tricyclic antidepressants, or diuretics
• Take any chronic medication that has not had a stable dose for 1 month or longer
• Have type 1 or type 2 diabetes
• Have any significant cardiac disease (such as heart failure, arrhythmias, or valve disease), uncontrolled pulmonary disease, chronic liver disease, chronic kidney disease, or chronic infectious disease
• Have any significant psychiatric illness that is unstable or untreated such as bipolar disorder, severe depression, or severe anxiety
• Have a history of suicidal ideation
• Have an allergy or hypersensitivity to albuterol
• Are unwilling to discontinue caffeine-containing products while in the study
• Are deemed unfit to participate in the study based on evaluation by the medical investigator

• Minimum Eligible Age: 12 Years
• Maximum Eligible Age: 17 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Leverage Innovation for Technology Transfer Fund (LSU LIFT2)

UNKNOWN

Sponsor Role: collaborator

Pennington Biomedical Research Center

OTHER

Sponsor Role: lead

Responsible Party

Daniel Hsia

Assistant Professor

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Daniel Hsia, PhD

Role: PRINCIPAL_INVESTIGATOR

Pennington Biomedical Research Center

Locations

Pennington Biomedical Research Center

Baton Rouge, Louisiana, United States

Countries

United States

References

Liu AG, Arceneaux KP 3rd, Chu JT, Jacob G Jr, Schreiber AL, Tipton RC, Yu Y, Johnson WD, Greenway FL, Primeaux SD. The effect of caffeine and albuterol on body composition and metabolic rate. Obesity (Silver Spring). 2015 Sep;23(9):1830-5. doi: 10.1002/oby.21163. Epub 2015 Aug 4.

Reference Type: BACKGROUND

PMID: 26239482 (View on PubMed)

Skura CL, Fowler EG, Wetzel GT, Graves M, Spencer MJ. Albuterol increases lean body mass in ambulatory boys with Duchenne or Becker muscular dystrophy. Neurology. 2008 Jan 8;70(2):137-43. doi: 10.1212/01.WNL.0000287070.00149.a9. Epub 2007 Oct 17.

Reference Type: BACKGROUND

PMID: 17942817 (View on PubMed)

Caruso JF, Hamill JL, De Garmo N. Oral albuterol dosing during the latter stages of a resistance exercise program. J Strength Cond Res. 2005 Feb;19(1):102-7. doi: 10.1519/R-14793.1.

Reference Type: BACKGROUND

PMID: 15705021 (View on PubMed)

Provided Documents

Document Type: Study Protocol and Statistical Analysis Plan

View Document

Other Identifiers

PBRC 2015-065

Identifier Type: -

Identifier Source: org_study_id