Las Vegas, NVNCT05653102Now EnrollingIRB Ready

Knee Arthroplasty, Total Clinical Trial in Las Vegas, NV

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

Sponsored by Exactech

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Expert Care in Las Vegas

Access knee arthroplasty, total specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related knee arthroplasty, total treatment provided free

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Check if you qualify for this knee arthroplasty, total clinical trial in Las Vegas, NV

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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 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 Knee Arthroplasty, Total Study in Las Vegas

A Post-Market Domestic (US) and International Data Collection to Assess the Truliant® Knee System

Sponsor: Exactech

Who Can Participate

Inclusion Criteria

Cohort 1. Prospective / Subjects- Enrolled in the study pre-surgery
Subjects who agree to participate in the study that have not had surgery prior to being enrolled in the study.
Skeletally mature (18 years of age or older).
Subject is willing and able to provide written informed consent for participation in the study.
Subject is to receive a Truliant® total knee replacement for Osteoarthritis, Avascular Necrosis, Rheumatoid Arthritis, Post-Traumatic Arthritis, Polyarthritis, Primary Implantation Failure, or as a Conversion of Uni-Compartmental Knee.
The knee replacement will be performed by the investigator or a surgeon sub-investigator.
The devices will be used according to the approved indications. Cohort 2. Retrospective to Prospective / Subjects enrolled in the study post- surgery then continue to participate in the study prospectively.
Subjects who agree to participate in the study that have undergone surgery prior to enrollment in the study. Data for these subjects will collected from the subject's medical record for the time period prior to enrollment in the study containing data pertaining to the index surgery (retrospective data) and from the patient after they are enrolled in the study during the post-operative time period (prospectively).
Skeletally mature (18 years of age or older).
Subject is willing and able to provide written informed consent for participation in the study.
Subject received a Truliant® total knee replacement for Osteoarthritis, Avascular Necrosis, Rheumatoid Arthritis, Post-Traumatic Arthritis, Polyarthritis, Primary Implantation Failure, or as a Conversion of Uni-Compartmental Knee.
The knee replacement was performed by the investigator or a surgeon sub-investigator.
The devices are/were used according to the approved indications.
Special consideration should be taken to ensure that these subjects meet all inclusion criteria, none of the

Exclusion Criteria

, and have a minimum of the following pre-operative, operative, and applicable postoperative data available in the subject's medical records, related to the Truliant® knee prosthesis manufactured or distributed by Exactech Inc (Gainesville, Florida, USA). Prior to inclusion in the study, the following details must be available for data submission: Pre-Operative: o Demographic Data
Age at surgery
Height/Weight
Indication for surgery
Prior Injuries/Surgeries on index knee
Comorbidities
Date of Surgery
Type of Surgery (Primary / Revision)
All component product information, including catalogue reference numbers
Adverse Event Information, if applicable Cohort 3. Retrospective Only Subjects enrolled in the study post-study surgery with no intent to continue as prospective subjects. Note: No prospective data may be collected from a subject if they are enrolled under this cohort unless the subject is willing and able to provide written informed consent for participation in the study.
Skeletally mature at the time of the surgery (18 years of age or older).
The patient's clinical record includes a signed HIPAA waiver allowing for the use of clinical record data for the purpose of clinical research outside of the operating institution.
The patients clinical record includes a documented procedure that includes, or is related to, TKA with a Truliant® Knee system device.
The knee replacement was performed by the investigator or a surgeon sub-investigator.
The devices are/were used according to the approved indications.
Special consideration should be taken to ensure that these subjects meet all inclusion criteria, none of the exclusion criteria and have a minimum of the following pre-operative, operative, and applicable postoperative data available in the subject's medical records, related to the Truliant® knee prosthesis manufactured or distributed by Exactech Inc (Gainesville, Florida, USA). Prior to inclusion in the study, the following details must be available for submission:
Pre-Operative:
Demographic Data
Age at surgery
Height/Weight
Indication for surgery
Prior Injuries/Surgeries on index knee
Comorbidities
Date of Surgery
Type of Surgery (Primary / Revision)
All component product information, including catalogue reference numbers Adverse Event Information, if applicable Exclusion Criteria:
Patient was \<18 years of age at time of surgery
Patient does not meet indicated population for use criteria for this device
Patient is pregnant
Patient is a prisoner
Patient has a physical or mental condition that would invalidate the results
Patient is contraindicated for the surgery (e.g., metal allergy)

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 (NCT05653102) 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.

Knee Arthroplasty, Total Treatment Options in Las Vegas, NV

If you're searching for knee arthroplasty, total treatment options in Las Vegas, NV, this clinical trial (NCT05653102) 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 knee arthroplasty, total 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 knee arthroplasty, total clinical trials near you to find additional studies recruiting in your area.

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