Association of Beta-2 Adrenergic Agonist and Corticosteroid Injection in the Treatment of Lipomas
Primary Purpose
Lipoma
Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Prednisolone synthetic cortisone and Isoproterenol together
Sponsored by
About this trial
This is an interventional treatment trial for Lipoma focused on measuring Obesity therapy, fat, drug mechanism, adipose tissue, cellular pharmacology
Eligibility Criteria
Inclusion Criteria:
- You are a man or a woman between the ages of 18-60, inclusive.
- You have a body mass index (BMI) between 20 and less than 40 kg/m2. BMI is a number calculated from your height and weight.
- You have a lipoma (a benign fatty tumor) that is 1 inch or more in diameter under the skin of your abdomen or on another area of your body that is easily accessible to study (such as the thigh).
- You have not gained or lost more than 11 pounds in the last 3 months.
- Your exercise routine has been stable for the last 3 months or you are sedentary. Sedentary means you do less than 60 minutes of exercise per week.
Exclusion Criteria:
- You have a history of heart or blood vessel disease.
- Your blood pressure is above 140/90 mmHg.
- You have type 1 diabetes.
- You have a history of kidney or liver disease.
- You have thyroid disease that has not been treated.
- You are a smoker.
- You use a Beta-2 (B2) adrenergic stimulator (a type of drug used to treat asthma), a beta adrenergic blocker (a type of drug used to treat blood pressure) or glucocorticoid medications (a type of drug used to treat immune system disease).
- You have a problem with alcoholism or other substance abuse.
- You are pregnant or breast feeding.
Sites / Locations
- Pennington Biomedical Research Center
Arms of the Study
Arm 1
Arm Type
Other
Arm Label
Prednisolone and Isoproteronol Together
Arm Description
Beta-adrenergic agonists and corticosteroid
Outcomes
Primary Outcome Measures
The Average Percent Volume Reduction in the Lipoma.
Secondary Outcome Measures
The Number of Lipoma Increased in Volume.
The Number of Subjects Elected to Have the Lipoma Removed.
Full Information
NCT ID
NCT00624416
First Posted
February 15, 2008
Last Updated
December 17, 2015
Sponsor
Pennington Biomedical Research Center
Collaborators
Lipothera
1. Study Identification
Unique Protocol Identification Number
NCT00624416
Brief Title
Association of Beta-2 Adrenergic Agonist and Corticosteroid Injection in the Treatment of Lipomas
Official Title
A Pilot Study: Association of Beta-2 Adrenergic Agonist and Corticosteroid Injection in the Treatment of Lipomas
Study Type
Interventional
2. Study Status
Record Verification Date
December 2015
Overall Recruitment Status
Completed
Study Start Date
October 2007 (undefined)
Primary Completion Date
March 2009 (Actual)
Study Completion Date
March 2009 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Pennington Biomedical Research Center
Collaborators
Lipothera
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this study is to test whether injected medications will increase the amount of fat released by a fat cell. We will compare prednisolone (a synthetic cortisone) combined with isoproterenol (a drug given for asthma) versus using isoproterenol alone. We will also test if injections of isoproterenol and prednisolone will shrink the size of lipomas, which are benign fatty tumors.
Detailed Description
Lipomas are benign, non-cancerous fatty tumors that occur under the skin and make a bump that can be easily felt and often seen. The current treatment for lipomas is surgery. Isoproterenol, a medication used for the treatment of asthma and approved for injection under the skin, is known to cause fat cells to give up their fat. The fat cells become resistant to isoproterenol with repeated use. Prednisolone, a synthetic cortisone medication used to treat immune problems like allergy and approved for injection under the skin, keeps the fat cells from becoming resistant to isoproterenol. It is not known, if the fat cells in lipomas act like other fat cells or if the combination of isoproterenol and prednisolone injections would shrink lipomas without surgery. This study is designed to test this possibility.
Subjects will have a screening visit, 2 microdialysis visits a week apart, 20 treatment visits 5 days per week for 4 weeks, and up to 12 follow-up visits a year after treatment visits. During screening, subjects will have a history, physical exam, blood testing, electrocardiogram and a pregnancy testing if female with reproductive capacity. The first microdialysis visit will consist of placing two microdialysis catheters under the skin after the area is numbed. One microdialysis catheter will be in the lipoma and the other under the skin 2 inches away. The microdialysis catheter will connect to a pump, isoproterenol will be infused and the amount of fat breakdown measured. One week later prednisolone will be injected into the lipoma and under the skin 2 inches away. The microdialysis visit will be repeated 24 hours later.
Treatment will consist of injecting the lipoma 5 days a week with a mixture of isoproterenol and prednisolone in the Pennington clinic as a diabetic would inject insulin. Each week the blood pressure, pulse and lipoma will be measured and subjects will be asked how they feel. At the end of the treatment period the physical examination, blood test and electrocardiogram will be repeated.
The insertion of the microdialysis probes under the skin into the fat tissue could be uncomfortable, but numbing medication will be injected first to prevent this problem. At higher doses, isoproterenol could lower blood pressure and increase pulse rate. This should not happen at the doses used, but blood pressure and pulse will be monitored throughout the study. Prednisolone, at higher doses, could decrease the body's production of cortisone. This should not happen at the doses being used, but cortisone in the body will be measured during the trial. Blood tests involve the discomfort of a needle going through the skin of the arm, possible bruising and rarely fainting or infection. Trained technicians and sterile needles will minimize these risks.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Lipoma
Keywords
Obesity therapy, fat, drug mechanism, adipose tissue, cellular pharmacology
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
10 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Prednisolone and Isoproteronol Together
Arm Type
Other
Arm Description
Beta-adrenergic agonists and corticosteroid
Intervention Type
Drug
Intervention Name(s)
Prednisolone synthetic cortisone and Isoproterenol together
Other Intervention Name(s)
Prednisolone combined with Isoproterenol
Intervention Description
Approximately 0.2 to 0.4cc of isoproterenol-prednisolone solution (0.04 - 0.08 mg isoproterenol and 0.07 - 0.14 mg prednisolone) in one or more sites in the lipoma depending on its size, 5 days a week for 4 weeks.
Primary Outcome Measure Information:
Title
The Average Percent Volume Reduction in the Lipoma.
Time Frame
Baseline and 4 weeks
Secondary Outcome Measure Information:
Title
The Number of Lipoma Increased in Volume.
Time Frame
After four weeks of treatment up to one year.
Title
The Number of Subjects Elected to Have the Lipoma Removed.
Time Frame
After four weeks up to one year.
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
You are a man or a woman between the ages of 18-60, inclusive.
You have a body mass index (BMI) between 20 and less than 40 kg/m2. BMI is a number calculated from your height and weight.
You have a lipoma (a benign fatty tumor) that is 1 inch or more in diameter under the skin of your abdomen or on another area of your body that is easily accessible to study (such as the thigh).
You have not gained or lost more than 11 pounds in the last 3 months.
Your exercise routine has been stable for the last 3 months or you are sedentary. Sedentary means you do less than 60 minutes of exercise per week.
Exclusion Criteria:
You have a history of heart or blood vessel disease.
Your blood pressure is above 140/90 mmHg.
You have type 1 diabetes.
You have a history of kidney or liver disease.
You have thyroid disease that has not been treated.
You are a smoker.
You use a Beta-2 (B2) adrenergic stimulator (a type of drug used to treat asthma), a beta adrenergic blocker (a type of drug used to treat blood pressure) or glucocorticoid medications (a type of drug used to treat immune system disease).
You have a problem with alcoholism or other substance abuse.
You are pregnant or breast feeding.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Leanne Redman, Ph.D.
Organizational Affiliation
Pennington Biomedical Research Center
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Frank Greenway, M.D.
Organizational Affiliation
Pennington Biomedical Research Center
Official's Role
Study Director
Facility Information:
Facility Name
Pennington Biomedical Research Center
City
Baton Rouge
State/Province
Louisiana
ZIP/Postal Code
70808
Country
United States
12. IPD Sharing Statement
Learn more about this trial
Association of Beta-2 Adrenergic Agonist and Corticosteroid Injection in the Treatment of Lipomas
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