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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01611519
Other study ID # 11-006618
Secondary ID
Status Completed
Phase N/A
First received June 1, 2012
Last updated September 12, 2016
Start date December 2011
Est. completion date October 2014

Study information

Verified date September 2016
Source Mayo Clinic
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

Is the early removal of Foley catheter safe in patients undergoing general thoracic surgery with an epidural catheter in place?


Description:

We hypothesis that removing the foley catheter within 48 hours after a thoracotomy in patients that have an epidural catheter will result in an increase in the rate of urinary infections and the need for reinsertion of the foley. We have designed a randomized trial to test this hypothesis.


Recruitment information / eligibility

Status Completed
Enrollment 375
Est. completion date October 2014
Est. primary completion date October 2014
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- epidural catheter after thoracic surgery

- foley in place

Exclusion Criteria:

- < 18 years of age

- death in hospital within 30 days of the operation

- length of hospital stay is less than 48 hours

- epidural catheter is removed before the 3rd postoperative day

- patients who have a suprapubic catheter or no bladder

- patients who require a urologist or a urologic technician to insert the Foley catheter at the time of surgery

- patients who were being intermittently catheterized before surgery

- patients with a known urinary tract infection preoperatively

- patients required to keep Foley in since they required close monitoring of urinary output

Study Design

Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
United States Mayo Clinic in Rochester Rochester Minnesota

Sponsors (1)

Lead Sponsor Collaborator
Mayo Clinic

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Need for insertion of catheter after Foley removed. participants will be followed for the duration of hospital stay, an expected average of 5 weeks No
Secondary Development of urinary tract infection participants will be followed for the duration of hospital stay, an expected average of 5 weeks No
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