Destin, FLNCT04779918Now EnrollingIRB Ready

Hernia, Ventral Clinical Trial in Destin, FL

Access cutting-edge hernia, ventral treatment through this clinical trial at a research site in Destin. Study-provided care at no cost to qualified participants.

Sponsored by Tela Bio Inc

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Expert Care in Destin

Access hernia, ventral specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related hernia, ventral treatment provided free

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Check if you qualify for this hernia, ventral clinical trial in Destin, FL

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

Why Participate?

  • No-Cost Study Care

  • Local to Destin

    Convenient for FL 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 Destin site if eligible
  4. 4Begin participation

About This Hernia, Ventral Study in Destin

This study is designed to evaluate the post-operative complications and hernia recurrence following the use of OviTex in subjects with ventral or inguinal hernias. Up to 160 subjects will participate in the study from up to 20 investigator sites.

Sponsor: Tela Bio Inc

Who Can Participate

Inclusion Criteria

Subject suffers from a ventral or inguinal hernia that requires surgical repair with the use of an implant to reinforce or replace weakened or missing tissue.
The patient is scheduled for an elective robotic approach with the use of OviTex LPR, OviTex Core Permanent, OviTex 1S Permanent, or OviTex IHR.
The size of the implant needed for repair is expected to be less than or equal to 15 x 25 cm for OviTex LPR and 25 x 40 cm for OviTex Core Permanent and OviTex 1S Permanent, with no size limitation for OviTex IHR.
Subject meets CDC/SSI Wound Classification Class I (Clean), Class II (Clean-Contaminated) or Class III (Contaminated) criteria.
Subject is willing and able to sign an informed consent for the study and has signed the IRB approved Informed Consent form for this study.
Subject is able to complete Quality of Life (QoL) and pain questionnaires.
Subject is at least 21 years old.
Subject is willing to comply and able to participate fully in, and for the full duration of, the study including follow-up requirements.

Exclusion Criteria

at Baseline:
Subject has a BMI of \> 40
Subject meets CDC/SSI Wound Classification Class IV (Dirty-Infected) criteria
Subject is female and is pregnant or plans to become pregnant during the course of the study.
Subject has a life expectancy of \< 2 years making it unlikely that the subject will successfully achieve two-year follow-up.
Subject has recent history of drug or alcohol abuse (in last 3 years).
Subject has an allergy to ovine-derived products.
Subject has participated in another clinical trial within the past 30 days or is currently involved in another clinical trial.
Subject has a strangulated hernia. Exclusion Criteria Intraoperative:
Subject requires implant that cannot be introduced into the surgical site during the procedure via port or an existing incision.
Subject unable to receive OviTex LPR, OviTex Core Permanent, OviTex 1S Permanent, or OviTex IHR at time of surgery.

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 Destin?

Yes, this clinical trial (NCT04779918) has an active research site in Destin, FL 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.

Hernia, Ventral Treatment Options in Destin, FL

If you're searching for hernia, ventral treatment options in Destin, FL, this clinical trial (NCT04779918) 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 Destin research site is actively enrolling participants for this clinical trial. You'll receive care from experienced hernia, ventral 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 hernia, ventral clinical trials near you to find additional studies recruiting in your area.

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Secure · Expert Care · Destin, FL