CompletedNot Applicable

Adverse Events in Dry Needling

United States250 participantsStarted 2018-08-01

Plain-language summary

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.

Who can participate

Age range18 Years – 100 Years

SexALL

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Inclusion Criteria: * Any patient that receives dry needling as a part of their care by a physical therapist and consents to provide information Exclusion Criteria: * Does not receive dry needling or does not consent to provide information

What they're measuring

Adverse event

Timeframe: 1 week

Trial details

NCT IDNCT03612843

SponsorElizabeth Lane

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2018-12-30

View on ClinicalTrials.gov More Muscle Soreness trials