Adverse Events in Dry Needling
Completed
Conditions studied: Muscle Soreness, Headache, Knee Osteoarthritis, Back Pain, Neck Pain, Needle Stick, Shoulder Pain, Hip Osteoarthritis
In brief
The purpose of this prospective cohort survey study is to further explore the incidence of adverse events with dry needling by physical therapists - as well as any differences or similarities between patient-reported vs therapist-reported incidence of AEs.
Key facts
- Study ID
- NCT03612843
- Run by
- Elizabeth Lane
- People needed
- 250
- Starts
- 2018-08-01
- Expected to finish
- 2018-12-30
- Last updated by the study team
- 2019-04-18
Who can join
Age: 18 and older, up to 100. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Any patient that receives dry needling as a part of their care by a physical therapist and consents to provide information
You may not qualify if…
- Does not receive dry needling or does not consent to provide information
Where it is running
- Benchmark Physical Therapy — Acworth, Georgia, United States
- Benchmark Physical Therapy — Cartersville, Georgia, United States
- Benchmark Physical Therapy — Fort Oglethorpe, Georgia, United States
- Benchmark Physical Therapy — Marietta, Georgia, United States
- Benchmark Physical Therapy — Roswell, Georgia, United States
- Benchmark Physical Therapy — Athens, Tennessee, United States
- Benchmark Physical Therapy — Hixson, Tennessee, United States
- Benchmark Physical Therapy — Kingsport, Tennessee, United States
Full record on ClinicalTrials.gov
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