Radiotherapy Compared to Corticosteroid Injection for Treatment of Hand Osteoarthritis

Part of paid clinical trials in Rochester, Minnesota.

Sponsor
Mayo Clinic
Study ID
NCT07217405
Phase
PHASE4
Status
Recruiting

Conditions

  • Osteoarthritis Hand
  • Osteoarthritis Wrist

Eligibility Criteria

Sex
ALL
Age
50 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Corticosteroid injection (CSI) — DRUG
    A maximum of 3 joints will be treated with standard a standard combination of methylprednisolone and lidocaine: * 1st Carpometacarpal (CMC) joint - 20 mg methylprednisolone/0.5 mL 1% lidocaine\* * Radiocarpal (RC) joint - 40 mg methylprednisolone/1 mL 1% lidocaine\* * Scaphotrapeziotrapezoidal (STT) joint - 20 mg methylprednisolone/0.5 mL 1% lidocaine\* * Metacarpophalangeal (MCP) joint - 20 mg methylprednisolone/0.5 mL 1% lidocaine * Interphalangeal (IP) joint - 10 mg methylprednisolone/0.25 mL 1% lidocaine
  • Low-dose radiotherapy (LDRT) — RADIATION
    Subjects will be treated with low-dose radiotherapy of 300cGy in 6 fractions, 2-3 times per week on non-consecutive days. Non-responders to the initial LDRT treatment will receive a second treatment course of 300cGy in 6 fractions to be given 2-3 times per week on non-consecutive days.

Study Details

The purpose of this research is to compare low-dose radiotherapy to corticosteroid injection for treatment of hand/wrist osteoarthritis.

Key Dates

Start date
Dec 19, 2025
Status verified
Apr 2026
Primary completion
May 1, 2027
Completion
Oct 1, 2027

Study Design

Enrollment
165 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Experimental: Low-dose radiotherapy (LDRT)
    Subjects will receive a total of six (6) low-dose radiotherapy (LDRT) treatments for hand osteoarthritis.
  • Active Comparator: Corticosteroid injection (CSI)
    Subjects will receive standard of care corticosteroid injection (CSI) therapy for hand osteoarthritis.

Primary Outcome Measure

Change in Visual Analog Scale (VAS) score [ Time Frame: Baseline, monthly for 6 months post-intervention, 9 months post-intervention, 12 months post-intervention ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
Mayo Clinic in RochesterRochesterMinnesota55905
Tochukwu Iyke-Nzeocha
(507) 422-3201
Melissa Wang, M.A., CCRP
(507) 266-6911
Terin Sytsma, MD (PRINCIPAL_INVESTIGATOR)

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