MedTrace Logo

LINQ® Procedure vs. Conventional Medical Management for Sacroiliac Dysfunction

NCT07558278 · Status: NOT_YET_RECRUITING · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 200

Last updated 2026-05-15

No results posted yet for this study

Summary

The objective of this clinical evaluation is to assess the safety and effectiveness of LINQ fusion procedure for treatment of sacroiliac joint (SIJ) dysfunction compared to Conservative Medical Management (CMM).

Conditions

  • Sacroiliac Joint Pain

Interventions

PROCEDURE

Bone Allograft

The LINQ system is intended for use in patients with SIJ disease by implantation of compatible implants to prepare the SIJ for allograft fusion.

OTHER

Conventional Medical Management (CMM)

CMM Control Arm shall receive standardized, stepwise, non-surgical management for SIJ pain.

Sponsors & Collaborators

  • PainTEQ, LLC

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
CROSSOVER

Eligibility

Min Age
21 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-07-01
Primary Completion
2027-12-01
Completion
2029-07-01

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07558278 on ClinicalTrials.gov