ReneuRx™ for Lateral Hip Pain

This study is looking at a new device called ReneuRx™ for people with moderate to severe chronic lateral hip pain (pain on the outside of the hip). It will compare ReneuRx™ to a common treatment, a single injection of Triamcinolone acetate (a steroid) into the hip joint. ReneuRx™ will be injected around specific nerves in the hip. The study wants to see how safe ReneuRx™ is and how well it helps with pain. You might be able to join if you are between 22 and 80 years old, have significant hip pain despite current treatments, and tenderness in the hip area. The study will follow participants for about 6 to 12 months to see how they are doing. The current status of this study is unclear.

Study design
This is an interventional study with a planned enrollment of 100 participants. It compares the ReneuRx™ device to Triamcinolone acetate injections.
What's involved
You would attend study visits, complete quality of life questionnaires, and be followed for approximately 6-12 months after the study procedure.
Compensation
Not stated in the trial record.
Follow-up
Participants will be followed for approximately 6-12 months after the study procedure, with safety measured through study completion (an average of 12 months).

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT07568015

ReneuRx™ (Nerve Selective Therapy) Utilized in Lateral Hip Pain

Not Yet Recruiting
NAAges 22–80InterventionalTreatment
Brixton Biosciences, Inc.
~100 participants
Updated 2026-06-29 on ClinicalTrials.gov
What's tested:Triamcinolone acetateReneuRx

At a glance

Recruiting sites
0 of 11 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Primary Effectiveness
Measured over 3-months post treatment
+1 more outcome measured
Greater Trochanteric Pain Syndrome
Greater Trochanteric Pain Syndrome of Both Lower Limbs
Lateral Hip Pain
11 sites across 8 states
Massachusetts2
Pennsylvania2
Texas2
Arizona1
Georgia1
Louisiana1
New Jersey1
Oklahoma1

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  • Primary Effectiveness3-months post treatment

    The primary endpoint of this study is the proportion of subjects whose hip pain following activity (Timed Up and Go test) is reduced by ≥30% based on the NRS scale at 3 months post treatment

  • Primary SafetyThrough study completion, an average of 12-months

    Aggregate serious device-related adverse events through final follow-up visit