Las Vegas, NVNCT06578650Now EnrollingIRB Ready

Surgical Wound Clinical Trial in Las Vegas, NV

Access cutting-edge surgical wound treatment through this clinical trial at a research site in Las Vegas. Study-provided care at no cost to qualified participants.

Sponsored by Acera Surgical, Inc.

Quick Self-Assessment

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Preparing your pre-screening questions…

Expert Care in Las Vegas

Access surgical wound specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related surgical wound treatment provided free

Apply for This Las Vegas Location

Check if you qualify for this surgical wound clinical trial in Las Vegas, NV

Secure & Confidential

Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to Las Vegas

    Convenient for NV residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Las Vegas site if eligible
  4. 4Begin participation

About This Surgical Wound Study in Las Vegas

The goal of this observational prospective study is to evaluate wound healing outcomes in resection wounds resulting from surgical removal of cutaneous malignancies treated with a synthetic electrospun fiber matrix. This study intends to quantify the time from initial resection and product application to time of complete granulation of the wound bed in weeks.

Sponsor: Acera Surgical, Inc.

Who Can Participate

Inclusion Criteria

Patient is at least 18 years old
Patient plans to undergo surgical resection of a cutaneous neoplasm
Patient is willing and capable of complying with all protocol requirements
Patient or legally authorized representative (LAR) is willing to provide written informed consent prior to participation in study
Post-resection surgical wound with a surface area of ≥4 cm2 and ≤ 36cm2

Exclusion Criteria

Inability to give informed consent or to complete the procedures required for study completion
Patient has been previously enrolled into this study, or is currently participating in another drug or device study that has not reached its primary endpoint
Patient is pregnant, breast feeding or planning to become pregnant
Patient has a known allergy to resorbable suture materials, e.g. Polyglactin 910 (PGLA), Polydioxanone (PDS)
Patients receiving any immunotherapy, radiation, or chemotherapy within the past four weeks prior to resection surgery.
Patient has a life expectancy less than six months as assessed by the investigator
Patient has an additional non-study related wound within 3 cm of the study wound
Study wound is located on the hands or feet
Patient has been diagnosed with osteomalacia
Resection defect from a squamous cell carcinoma arising from a chronic wound
Patient has an uncontrolled thyroid disorder
Hgb A1c \> 12% within 3 months prior to enrollment in patients with a known history of diabetes
Patient has a BMI \> 34.9
Patient has used any tobacco product within the past 30 days prior to surgery
Patients with chronic kidney disease on peritoneal or hemodialysis, or with an estimated glomerular filtration rate less than 15mL/min
Patients with severe liver disease with active cirrhosis defined as a gross ascites upon clinical exam or a Model for End-stage Liver Disease (MELD)-Na score greater than 15
Patient not in reasonable metabolic control in the judgement of the investigator
Patient has a known history of poor compliance with medical treatment
Patient has a history of radiotherapy to wound bed of interest
Patient has been diagnosed with at least one of the following autoimmune connective tissue diseases: lupus, vasculitis, sickle cell, or uncontrolled rheumatoid arthritis
Active infection, undrained abscess, or critical colonization of the wound with bacteria in the judgement of the investigator

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 Las Vegas?

Yes, this clinical trial (NCT06578650) has an active research site in Las Vegas, NV 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.

Surgical Wound Treatment Options in Las Vegas, NV

If you're searching for surgical wound treatment options in Las Vegas, NV, this clinical trial (NCT06578650) 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 Las Vegas research site is actively enrolling participants for this clinical trial. You'll receive care from experienced surgical wound 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 surgical wound clinical trials near you to find additional studies recruiting in your area.

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