Is NCT07820397 recruiting in Concord, OH?

Yes, NCT07820397 is currently recruiting participants at its Concord, OH location. This liposuction clinical trial is actively enrolling qualified participants.

How do I join the liposuction clinical trial in Concord?

To join this clinical trial in Concord, complete the eligibility form on this page. A study coordinator will contact you to discuss next steps and determine if you qualify.

Is participation in this Concord clinical trial free?

Yes, all study-related care is provided at no cost to qualified participants. Many studies also offer compensation for time and travel expenses.

Liposuction Clinical Trial in Concord, OH

About This Liposuction Study in Concord

This study will evaluate and compare the quality of adipose (fat) tissue harvested using different liposuction technologies and aspiration methods. Each participant will serve as their own control, with paired fat samples collected from anatomically matched treatment areas. The study will evaluate adipocyte viability and other characteristics of the harvested tissue, including viable adipocyte density, stromal vascular fraction, metabolic activity, and fat composition. The goal of the study is to better understand how different liposuction technologies and aspiration methods affect the quality and characteristics of harvested adipose tissue.

Sponsor: Apyx Medical

Who Can Participate

Inclusion Criteria

Male or female aged 30 to 65 years, inclusive.

Planned elective liposuction/body contouring procedure involving two or more anatomical areas (e.g., arms, abdomen, flanks, thighs, and/or back) with sufficient distribution to permit collection of paired adipose tissue samples from contralateral or anatomically matched treatment areas.

Investigator determines the subject is an appropriate candidate for the planned procedure and study participation.

Adequate adipose tissue is present to permit collection of required paired fat samples without impacting the planned surgical outcome.

Able to understand and sign the informed consent form.

Willing and able to comply with study requirements.

If applicable, female subjects of childbearing potential must have a negative urine pregnancy test on the day of procedure.

Exclusion Criteria

Prior liposuction or surgical intervention in the planned treatment areas that, in the opinion of the investigator, may affect adipose tissue characteristics or study assessments.

Prior treatment of the planned treatment areas with energy-based devices (e.g., ultrasound, radiofrequency, laser) that, in the opinion of the investigator, may affect adipose tissue characteristics or study assessments.

Significant skin laxity, fibrosis, scarring, or other abnormal tissue characteristics in the planned treatment areas that could impact fat harvest quality or comparability between sites.

Current smoker or use of nicotine-containing products within 4 weeks prior to the procedure.

Known metabolic or systemic conditions that may affect adipose tissue biology or wound healing, including but not limited to:

uncontrolled diabetes mellitus

significant vascular disease

connective tissue disorders

Use of medications known to significantly affect fat metabolism, tissue healing, or inflammatory response, including:

chronic systemic corticosteroids

immunosuppressive therapies

GLP-1 receptor agonists (e.g., semaglutide, tirzepatide) within 4 weeks prior to the procedure

Active local or systemic infection at the time of the procedure.

Known coagulopathy or use of anticoagulant therapy that cannot be safely discontinued prior to surgery.

Pregnant or breastfeeding subjects.

Body mass index (BMI) outside the range of 20-35 kg/m², inclusive.

Inadequate adipose tissue volume or distribution to permit paired sample collection from contralateral or anatomically matched areas.

Participation in another interventional clinical study that, in the opinion of the investigator, could interfere with study endpoints.

Any condition that, in the opinion of the investigator, would make the subject unsuitable for participation or could confound study results.

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Concord?

Yes, this clinical trial (NCT07820397) has an active research site in Concord, OH that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Liposuction Treatment Options in Concord, OH

If you're searching for liposuction treatment options in Concord, OH, this clinical trial (NCT07820397) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Concord research site is actively enrolling participants for this clinical trial. You'll receive care from experienced liposuction specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all liposuction clinical trials near you to find additional studies recruiting in your area.

Liposuction Clinical Trial in Concord, OH

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