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Battlefield Acupuncture With Sodium Hyaluronate Injections

Brooke Army Medical Center logo

Brooke Army Medical Center

Status

Unknown

Conditions

Knee Osteoarthritis

Treatments

Other: Battlefield Acupuncture

Study type

Interventional

Funder types

Other U.S. Federal agency

Identifiers

NCT03456011
OrthoDSC

Details and patient eligibility

About

The study evaluates pain relief and subsequent range of motion changes combining battlefield acupuncture with sodium hyaluronate vs local anesthetic and sodium hyaluronate

Full description

Sodium hyaluronate is FDA approved for knee osteoarthritis. It is a widely used treatment for this condition. This does provide immediate pain relief and is often used in conjunction with lidocaine and ropivacaine to both improve pain relief and treatment tolerance.

battlefield acupuncture has been showing promise as an adjunct pain relief treatment option. If used during intra articular visco supplementation knee injections, this may provide pain relief and positive changes in range of motion without the need of local anesthetic being injected into the joint space.

Enrollment

60 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Patients of the BAMC Orthopaedic clinic
  • Active duty, dependent and civilians
  • Ages 18-65
  • Diagnosed with knee osteoarthritis by their Orthopaedic provider
  • Determined to be eligible for Sodium Hyaluronate injections by their Orthopaedic provider

Exclusion criteria

  • Patient without knee osteoarthritis diagnosis
  • Patient requiring immediate surgery for their knee complaints
  • Patients younger than 18 or older than 65
  • Pregnant patients
  • Patients without active pain
  • Patients with history of knee arthroplasty
  • Patients with auricular deformity which would affect BFA
  • Patient with history of vasovagal secondary to needles or injections
  • Patients with active infection at BFA treatment sites

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

60 participants in 2 patient groups

BFA with Eufflexa injections
Other group
Description:
BFA treatment before Sodium Hyaluronate injections. Intervention: BFA
Treatment:
Other: Battlefield Acupuncture
Anesthetic with Eufflexa injections
No Intervention group
Description:
Receiving Standard of care determined by their provider No interventions

Trial contacts and locations

1

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Central trial contact

Christopher Gomez, MPAS

Data sourced from clinicaltrials.gov

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