Comparison of CornerLoc SI Joint Stabilization and Steroid Injections for Sacroiliac Joint Dysfunction

NCT ID: NCT04218838

Last Updated: 2023-06-15

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: NA
• Total Enrollment: 7 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2020-08-13
• Study Completion Date: 2022-01-01

Brief Summary

This study has been designed to compare the safety and effectiveness of the CornerLoc™ SI Joint Stabilization System to intra-articular sacroiliac joint steroid injection in patients with refractory sacroiliac joint dysfunction.

Detailed Description

Randomized, multicenter, open-label, randomized design to compare CornerLoc Allograft-based Sacroiliac Joint Stabilization System to Intra-articular Sacroiliac Joint Steroid Injection. Within the initial phase, referred to as the Randomized Phase, the primary determination of efficacy and safety will be 6-months following the study procedure. The analysis will be based on the randomization assignment. In the second phase of the study, referred to as the Cross-over Phase, patients who fail to respond to the randomized treatment assignment will be permitted to receive the non-randomized treatment. The basis of the sample size and hypothesis testing for this clinical investigation will be based on the Randomization Phase.

Conditions

Sacroiliac Joint Somatic Dysfunction

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

CornerLoc SI Joint Stabilization Group

Patient will receive the CornerLoc minimally invasive SI Joint Stabilization procedure. This procedure will be performed in an outpatient surgery center under local sedation or general anesthesia, and normally takes around 45 minutes. During the procedure, the physician will make two small incisions in the patient's lower back to access the SI joint, and place four small cadaveric bone grafts into the SI joint to help stabilize the SI joint.

Group Type: ACTIVE_COMPARATOR

CornerLoc SI Joint Stabilization Procedure

Intervention Type: DEVICE

CornerLoc minimally invasive SI Joint Stabilization System

SI Joint Steroid Injections Group

Patient will receive an injection of steroid medication directly into their SI joint. The area around the SI joint will be numbed with an injection of local anesthetic and then ultrasound guidance will be used to guide the needle of steroid medication directly into the SI joint. This procedure will be performed in the physician's office or an outpatient surgery center, and normally takes around 30 minutes.

Group Type: ACTIVE_COMPARATOR

Intra-articular Sacroiliac Joint Steroid Injection

Intervention Type: DRUG

Standard of Care - Steroid injection into the sacroiliac joint

Interventions

CornerLoc SI Joint Stabilization Procedure

CornerLoc minimally invasive SI Joint Stabilization System

Intervention Type: DEVICE

Intra-articular Sacroiliac Joint Steroid Injection

Standard of Care - Steroid injection into the sacroiliac joint

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Subject must provide written informed consent prior to any clinical study-related procedure.
• Subject is at least 18 years (or the minimum age required by local law to consent for participation in a clinical investigation) or older at the time of enrollment.
• Subjects must meet criteria for sacroiliac joint dysfunction as determined below:
• History of persistent pain in the distribution of the sacroiliac joint despite adequate trial of physical therapy.
• NRS for pain ≥ 7 on a 0 -.10-point scale.
• 3 of 5 provocative tests with positive findings on physical examination (SI distraction, thigh thrust, FABER, lateral compression, Gaenslen's maneuver).
• Positive response (≥75% percent pain relief) to diagnostic sacroiliac joint injection on two occasions at least one week apart.
• Baseline pain with 30-day history and PROMIS-29

Exclusion Criteria

• Patient will not be entered into the study if they meet one of the following criteria:

• Subject is unable to provide written informed consent
• Subject is enrolled, or intends to participate, in a clinical drug and/or device study (investigational device, investigational drug, new indication for a device or drug, or additional testing beyond standard of care procedures) which could confound the results of this trial as determined by the investigator.
• Presence of other anatomic or comorbid conditions, or other medical, social, or psychological conditions that, in the investigator's opinion, could limit the subject's ability to participate in the clinical investigation or to comply with follow-up requirements, or impact the scientific soundness of the clinical investigation results.
• Subject had prior surgical fusion implanted on same side
• Subject is pregnant or nursing
• Self-reported plan to bear children
• BMI ≥ 40
• DEXA < -2.5 (if available)
• History of microfractures
• History of compression fractures
• History of diabetes, must have A1c <8
• History of chronic steroid use
• Chronic immunosuppression

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

CornerLoc

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Michael Fishman, MD

Role: PRINCIPAL_INVESTIGATOR

Center for Interventional Pain & Spine

Locations

Center for Interventional Pain and Spine

Lancaster, Pennsylvania, United States

Countries

United States

Other Identifiers

COVI-0001

Identifier Type: -

Identifier Source: org_study_id