Status:

COMPLETED

Periosteal Electrical Dry Needling for Knee Osteoarthritis

Lead Sponsor:

Alabama Physical Therapy & Acupuncture

Collaborating Sponsors:

Universidad Rey Juan Carlos

Conditions:

Knee Osteoarthritis

Eligibility:

All Genders

18+ years

Phase:

NA

Brief Summary

The purpose of this research is to treat patients with knee osteoarthritis (OA) with periosteal electric dry needling (PEDN). It is also to determine the optimal "maintenance" regiment (i.e. maintenan...

Detailed Description

Patients with knee osteoarthritis will be randomized to receive periosteal electrical dry needling 1-2 treatments per week for 6 weeks (up to 10 sessions total) followed by either: 1. no maintenance t...

Eligibility Criteria

Inclusion

  • Adult over the age of 18 years old:
  • Report of knee pain of at least 2/10 per NPRS (0---10 scale) for \>3 months
  • Report of at least 3 of the following per Altman et al. (1986) (sensitivity = 95% / specificity = 69%)
  • Over 50 Years of age
  • Less than 30 minutes of morning stiffness
  • Crepitus on active motion
  • Bony tenderness
  • Bony enlargement
  • No palpable warmth of Synovium

Exclusion

  • Report of red flags to manual physical therapy to include: hypertension, infection, diabetes, peripheral neuropathy, heart disease, stroke, chronic ischemia, edema, severe varicosities, tumor, metabolic disease, prolonged steroid use, fracture, RA, osteoporosis, severe vascular disease, malignancy, etc.
  • History of physical therapy, massage therapy, chiropractic treatment, or injections for knee pain in last 4 weeks.
  • History of a partial or total knee replacement on the painful lower extremity.
  • History of a surgical procedure on either lower extremity in last 12 months.
  • Two or more positive neurologic signs consistent with nerve root compression, including any two of the following:
  • Weakness involving a major muscle group of the lower extremity.
  • Diminished patella or achilles tendon reflex
  • Diminished or absent sensation to pinprick in lower extremity dermatome.
  • Involvement in litigation or worker's compensation regarding knee pain.
  • Any condition that might contraindicate the use of periosteal electric dry needling
  • The patient is pregnant.

Key Trial Info

Start Date :

March 1 2021

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

May 1 2024

Estimated Enrollment :

586 Patients enrolled

Trial Details

Trial ID

NCT05365061

Start Date

March 1 2021

End Date

May 1 2024

Last Update

June 12 2024

Active Locations (1)

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Team Rehabilitation

Chamblee, Georgia, United States, 30341