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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04202315
Other study ID # STUDY00002673
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date January 15, 2019
Est. completion date June 1, 2020

Study information

Verified date December 2019
Source University of Washington
Contact Hunter Hoffman, PhD
Phone 2067442172
Email hunthoff@uw.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Assessing the role of virtual reality in decreasing pain and improving patient satisfaction in outpatient removal of pelvic external fixator constructs.


Recruitment information / eligibility

Status Recruiting
Enrollment 20
Est. completion date June 1, 2020
Est. primary completion date June 1, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- Pelvis external fixator placed at study institution

- External fixator placed for pelvic instability

Exclusion Criteria:

- Infected pin or pins

- Loose pin or pins

- Psych history

Study Design


Related Conditions & MeSH terms

  • Hip Fractures
  • Pelvic Fracture Pubic Rami Multiple - Unstable Closed

Intervention

Other:
Virtual Reality
Utilizing Virtual Reality during external fixator removal in outpatient clinic setting.

Locations

Country Name City State
United States University of Washington/Harborview Medical Center Seattle Washington

Sponsors (1)

Lead Sponsor Collaborator
University of Washington

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pain Score Pain score during removal of external fixator During procedure
Secondary Patient Satisfaction Self reported patient satisfaction, comparing no virtual reality to virtual reality immediately after procedure