LINQ® Procedure vs. Conventional Medical Management for Sacroiliac Dysfunction
ConditionSacroiliac Joint Pain
Trial statusNot yet recruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age21+
SponsorPainTEQ, LLC
About this trial
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).
Eligibility criteria
Qualifiers
Age and Body Mass Index (BMI)
Adult subjects aged ≥ 21 years at screening.
BMI ≤ 40.
Chronic SIJ-Related Pain
Disqualifiers
Pain Source Uncertainty a. Inability to confirm, in the Investigator's clinical judgment, that the subject's primary pain generator is the sacroiliac joint.
Alternative Primary Spine Pathology
Other Sacroiliac Pathology
Non-SIJ Pain Syndromes
Trial design
Treatments tested in this trial
- Bone Allograft
- Conventional Medical Management (CMM)
Treatment groups
200 Participants
are divided into 2 treatment groupsLocations
Sponsors and collaborators
Source ClinicalTrials.gov