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Adverse Events in Dry Needling

NCT03612843 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 250

Last updated 2019-04-18

No results posted yet for this study

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.

Conditions

Interventions

OTHER

Observational dry needle

No intervention provided by the study. Observation of any adverse events that occur surrounding dry needling by a physical therapist.

Sponsors & Collaborators

  • Brenau University

    collaborator OTHER

  • Elizabeth Lane

    lead OTHER

Eligibility

Min Age
18 Years
Max Age
100 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-08-01
Primary Completion
2018-12-30
Completion
2018-12-30

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03612843 on ClinicalTrials.gov