Boston, MANCT07059065Now EnrollingIRB Ready

Degenerative Spine Disease Clinical Trial in Boston, MA

Access cutting-edge degenerative spine disease treatment through this clinical trial at a research site in Boston. Study-provided care at no cost to qualified participants.

Sponsored by DePuy Synthes Products, Inc.

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Expert Care in Boston

Access degenerative spine disease specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related degenerative spine disease treatment provided free

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Check if you qualify for this degenerative spine disease clinical trial in Boston, MA

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Why Participate?

  • No-Cost Study Care

  • Local to Boston

    Convenient for MA 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 Boston site if eligible
  4. 4Begin participation

About This Degenerative Spine Disease Study in Boston

This is a post-market, prospective, controlled, multicenter clinical study to evaluate radiographic fusion and clinical outcomes of FIBERGRAFT™ Aeridyan Matrix bone graft substitute in subjects who undergo a 1-3 level instrumented lumbar posterolateral fusion surgery. This clinical study will be conducted at up to 10 clinical sites within the United States.

Sponsor: DePuy Synthes Products, Inc.

Who Can Participate

Inclusion Criteria

Subjects who require a 1-3 level instrumented PLF fusion in the lumbar spine in conjunction with a 1 to 2 consecutive level posterior lumbar interbody fusion procedure between L1-S1.
Skeletally mature subjects at least 18 years of age at the time of consenting.
Willing to provide voluntary written informed consent prior to participation in the clinical study.

Exclusion Criteria

Subjects who had previous fusion surgery at the index level(s).
Requiring a Posterolateral Fusion in the lumbar spine at more than three levels and/or an interbody fusion at more than two levels
Subjects who have demonstrated allergy or foreign body sensitivity to the implant or graft material.
Pregnant subjects or planning to become pregnant within the next 24 months.
Subjects diagnosed with severe osteoporosis which may prevent adequate fixation and thus preclude the use of these or any other orthopedic implant.
Subjects diagnosed with severe instabilities, vertebral fractures, spinal tumors.
Subjects who have an uncontrolled systemic or metabolic disease which, in the Investigator's opinion, would compromise their health, safety, or ability to participate or follow-up in this clinical study.
Subjects requiring use of an implantable bone graft stimulator or external bone graft stimulator.
Subjects that have infection or osteomyelitis at the graft site. Any medical or surgical condition that precludes the potential benefit of spinal surgery, in the opinion of the Investigator.
Any medical or surgical condition that precludes the potential benefit of spinal surgery, in the opinion of the Investigator.
Dependency on pharmaceutical drugs, drug abuse, or alcoholism resulting in a lack of subject cooperation.
Subjects unable to comply, and/or in the Investigator's opinion unable to comply, with the requirements of participation in the clinical study.
Enhanced Demineralized Bone Matrix product for the grafting control used within the posterolateral spine
Use of Bone Morphogenetic Protein (BMP) grafting material within the interbody cage(s).
Body Mass Index (BMI) ≥ 45
Unilateral posterior instrumentation
Subject is currently involved in a workers' compensation claim.
Subject has participated in an interventional clinical trial within the last 6 months or plans to participate in an interventional clinical trial within the next 24 months.

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 Boston?

Yes, this clinical trial (NCT07059065) has an active research site in Boston, MA 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.

Degenerative Spine Disease Treatment Options in Boston, MA

If you're searching for degenerative spine disease treatment options in Boston, MA, this clinical trial (NCT07059065) 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 Boston research site is actively enrolling participants for this clinical trial. You'll receive care from experienced degenerative spine disease 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 degenerative spine disease clinical trials near you to find additional studies recruiting in your area.

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