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NCT01577823 Clinical Trial

Utility of Indwelling Catheter in Orthopaedic Patients Receiving Spinal Anesthesia

Total Joint Arthroplasty Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01577823
Other study ID # RIJPARU2011
Secondary ID
Status Completed
Phase N/A
First received December 8, 2011
Last updated April 8, 2013

Study information
Verified date April 2013
Source Rothman Institute Orthopaedics
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

A study measuring utility of indwelling bladder catheter placement in orthopaedic surgical patients receiving spinal anesthesia. Study will track clinical outcomes, patient satisfaction and cost efficacy. Absence of indwelling bladder catheter may decrease urinary tract infection (UTI) incidence, increase patient satisfaction, and decrease cost burden without increasing postoperative urinary retention (POUR) incidence.

Recruitment information / eligibility
Status Completed
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

Elective orthopaedic surgical patients of all ages undergoing lower extremity adult reconstructive surgery with spinal anesthesia will be interviewed.

Exclusion Criteria:

Patients are excluded from the study preoperatively with a history of prostate or urological surgery, renal failure, previous documented POUR, current indwelling catheter, or acute UTI.

Study Design

N/A

Related Conditions & MeSH terms

Intervention

Device:
• Foley Catheter

Locations
Country Name City State
United States Rothman Institute Philadelphia Pennsylvania

Sponsors (1)
Lead Sponsor Collaborator
Rothman Institute Orthopaedics

Country where clinical trial is conducted

United States, 

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