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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT02807571
Other study ID # 2015-263
Secondary ID
Status Withdrawn
Phase
First received
Last updated
Start date February 10, 2017
Est. completion date October 3, 2017

Study information

Verified date September 2023
Source Spectrum Health Hospitals
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study is aimed at determining if office based surgery is an effective way of cutting health care cost while maintaining patient safety and satisfaction.


Description:

The study is a retrospective chart review with prospective patient satisfaction and functional outcome surveys. Patients that have had office based procedures that otherwise could be performed in the outpatient surgical setting from January 1, 2015 to December 4, 2015 will be contacted for study enrollment. Patient satisfaction and functional outcome surveys will be administered to those patients that consent to the research study. The data to be collected will include but is not limited to: age gender limb dominance, complications and co-morbidities.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date October 3, 2017
Est. primary completion date October 3, 2017
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Patients seen for office based procedures that otherwise would be performed in the outpatient surgical setting from January 1, 2015 to December 4, 2015 Exclusion Criteria: - K-wire hardware removal - Closed reductions - Patients receiving antibiotics at the time of the procedure

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Wide Awake Local Anesthesia No Tourniquet
Wide Awake Local Anesthesia No Tourniquet for office based hand surgery.

Locations

Country Name City State
United States Spectrum Health Grand Rapids Michigan

Sponsors (1)

Lead Sponsor Collaborator
Spectrum Health Hospitals

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Complication Rates Collect the incidence of complications. 2 months
Secondary Cost savings Compare the costs of the WALANT procedure with similar procedures done at an ASC or as an outpatient. 2 months
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