RECRUITING

Radio- KO Radiotherapy for Knee Osteoarthritis Clinical Trial

Description

The primary aim of this study is to investigate whether low-dose radiotherapy is an effective treatment to reduce the pain of knee osteoarthritis. A secondary aim is to determine whether patients experience any more measurable side effects than those receiving sham treatments.

Study Overview

Study Details

Study overview

The primary aim of this study is to investigate whether low-dose radiotherapy is an effective treatment to reduce the pain of knee osteoarthritis. A secondary aim is to determine whether patients experience any more measurable side effects than those receiving sham treatments.

The Randomized Clinical Trial of Low-Dose Radiotherapy for Knee Osteoarthritis

Radio- KO Radiotherapy for Knee Osteoarthritis Clinical Trial

Condition
Osteoarthritis, Knee
Intervention / Treatment

-

Contacts and Locations

Rochester

Mayo Clinic, Rochester, Minnesota, United States, 55905

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * age 50-85 years
  • * ICOAP pain scale A1 at least moderate intensity or B6 at least moderate intensity
  • * diagnosed with primary knee OA ICD-10 codes M17.x
  • * history of morning stiffness in knees that lasts less than 30 minutes
  • * history of crepitus without a history of warmth, redness or sudden onset of swelling
  • * physical exam findings of medial or lateral joint line tenderness on palpation that is in the same location as the knee pain for which their primary care provider has ordered an intraarticular steroid injection into the same knee.
  • * absence of primary knee pain in the pes anserine or hamstring or gastrocnemius tendons
  • * radiographic Kellgren-Lawrence grade 2-3 on 4-view knee x-rays taken within the last year
  • * ability to complete surveys in English
  • * Kellgren-Lawrence grade 1 or 4
  • * pregnancy or women 54 years and younger with potential for pregnancy (if they or their partner have not had tubal ligation, hysterectomy, or vasectomy)
  • * history of ipsilateral intraarticular knee surgery
  • * use of injected corticosteroids within 3 months or hyaluronans within 6 months or within 1 month if there was no sustained improvement post-injection of either corticosteroid or hyaluronan.
  • * history of trauma to this knee in the last year that clearly caused the pain now present
  • * history of RA, gout, pseudogout, hemarthroses (eg, hemophilic arthropathy) or other inflammatory arthritis involving this knee
  • * history of symptomatic hip OA
  • * history of psychosis, personality disorder, uncontrolled affective disorder
  • * history of fibromyalgia
  • * malignancy requiring active treatment
  • * current regular use of opiate analgesics, PRP, or acupuncture for the knees

Ages Eligible for Study

50 Years to 85 Years

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Mayo Clinic,

Stephen P. Merry, M.D., PRINCIPAL_INVESTIGATOR, Mayo Clinic

Paul D. Brown, M.D., PRINCIPAL_INVESTIGATOR, Mayo Clinic

Study Record Dates

2026-06-29