Nitrofurantoin Administration for the Prevention of Short-Term Catheter Associated Urinary Tract Infection After Pelvic Surgery (NAUTICA)
Primary Purpose
Catheter-Associated Urinary Tract Infection
Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Nitrofurantoin 100 MG
Placebo Oral Tablet
Sponsored by
About this trial
This is an interventional prevention trial for Catheter-Associated Urinary Tract Infection focused on measuring Nitrofurantoin, Prolapse, Pelvic Organ Prolapse, Anti-incontinence procedure, Urinary retention, Urinary Tract Infection, Short-term catheterization
Eligibility Criteria
Inclusion Criteria:
- Age greater than 18
- Creatinine clearance greater than 30 ml/min
- Failed postoperative hospital voiding trial
Exclusion Criteria:
- Pregnant
- History of glucose-6-phosphate dehydrogenase deficiency
- History of renal insufficiency, renal transplant, or nephropathy
- Allergy to nitrofurantoin
- History of recurrent UTI (defined as greater than two culture-proven infections in six months or three infections in one year)
- Urinary Tract Infection (UTI) within 14 days one month of surgery
- Non-English speaking
- Urinary tract infection while Foley catheter is in place
- On antibiotic therapy for other non-urological reasons
- Sustained intraoperative bladder injury requiring prolonged catheterization greater than 5 days
- Undergoing mesh excision from within the bladder, fistula repair, cystotomy repair, urethral diverticulectomy, sacral neuromodulation, urethral surgery, or any other procedure requiring prolonged catheterization and bladder decompression
- Placement of a suprapubic catheter
- Participants that request intermittent self-catheterization
- Neurologic conditions affecting urinary tract system and normal voiding mechanisms
- History of hepatic impairment due to prior nitrofurantoin use
- Inability to provide consent/decisionally impaired
- More than two in-office voiding trials
Sites / Locations
- Atrium Health
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Placebo Comparator
Arm Label
Nitrofurantoin
Placebo
Arm Description
Receives twice daily 100mg nitrofurantoin for 5 days following catheter removal
Receives twice daily matching placebo for 5 days following catheter removal
Outcomes
Primary Outcome Measures
UTI
Number of participants with a urinary tract infection in the first 30 days following pelvic reconstructive surgery
Secondary Outcome Measures
Adverse Events
Number of participants with an adverse event only related to study drug administration
Medication Compliance
Compliance assessed by use of a medication diary during treatment period
Full Information
NCT ID
NCT03287089
First Posted
September 15, 2017
Last Updated
August 5, 2022
Sponsor
Wake Forest University Health Sciences
1. Study Identification
Unique Protocol Identification Number
NCT03287089
Brief Title
Nitrofurantoin Administration for the Prevention of Short-Term Catheter Associated Urinary Tract Infection After Pelvic Surgery
Acronym
NAUTICA
Official Title
Nitrofurantoin Administration for the Prevention of Short-Term Catheter Associated Urinary Tract Infection After Pelvic Surgery (NAUTICA): A Randomized Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
May 2020
Overall Recruitment Status
Completed
Study Start Date
September 29, 2017 (Actual)
Primary Completion Date
May 30, 2019 (Actual)
Study Completion Date
June 1, 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Wake Forest University Health Sciences
4. Oversight
Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The specific aim of this randomized double-blind placebo-controlled trial is to evaluate the efficacy of administration of nitrofurantoin prophylaxis after catheter discontinuation for the prevention of catheter-associated urinary tract infections in patients with postoperative short-term catheterization following pelvic reconstructive surgery and/or urinary incontinence surgery.
Patients that undergo pelvic organ prolapse and/or urinary incontinence surgery and fail their post-operative voiding trial will be included in the study. Upon successfully passing and in-office voiding trial at the time of catheter removal, they will be randomized to either nitrofurantoin 100mg twice daily or an identical appearing placebo capsule twice daily for 5 days following catheter removal. The primary outcome will be the treatment of clinically suspected and/or culture-proven UTI within 30 days of surgery. Secondary outcomes include adverse events associated with nitrofurantoin use and medication compliance.
Primary and secondary outcomes will be evaluated with Student t test and chi squared or Fisher exact test as appropriate. Assuming a decrease in symptomatic UTIs attributable to nitrofurantoin prophylaxis from 32% to 14%, with 80% power, and a two-sided alpha of 0.05, we should recruit a total of 164 patients.
Detailed Description
Urinary tract infections (UTI) are the most common hospital-acquired infections, accounting for nearly 30% of cases of nosocomial infections and affecting nearly 1 million people per year.
Following pelvic reconstructive and urinary incontinence surgery, UTIs are one of the most common complications with a risk between 8.9%-34%. The baseline risk of UTI associated with pelvic floor surgery ranges between 5-35%, increasing greatly with catheterization.
Postoperative voiding dysfunction and incomplete bladder emptying is common following pelvic reconstructive and incontinence surgeries, with incidence ranging from 2.5 % to 31%. As a result, these women may have additional catheterization for a short period of time, which increases the risk of UTI. There is a 15-20% risk of developing a postoperative UTI with short-term catheterization, even if the catheter remains in place for merely 24 hours. The risk of UTI increases 5-10% each day the catheter is left in place.
Numerous studies have been conducted to evaluate different prophylactic antibiotic regimens to help decrease the rate of postoperative catheter-associated UTIs. Many of these studies have shown precedent for the use of antibiotic prophylaxis.
Nitrofurantoin has been evaluated as a prophylactic regimen for use during short-term catheterization. These studies had favorable results, decreasing the incidence of UTI postoperatively.
Although there are a few studies showing favorable results for the use of prophylactic nitrofurantoin during catheterization after pelvic surgery, the optimal timing of antibiotic administration and length of dosing regimen is not well defined. The American Urological Association (AUA) recommends empiric antibiotic treatment at the time of external urinary catheter removal in patients with risk factors, such as tobacco use, advanced age, and anatomic abnormalities of the urinary tract. The AUA Panel does cite that bacteriuria in the setting of noninfectious urinary tract disease is a risk factor for bacteremia, and, thus, prophylactic antibiotic treatment at time the of catheter removal may be indicated. The AUA does recommend empiric antibiotic treatment at the removal of an external urinary catheter in patients with risk factors. However, there is no standardization concerning the type of antibiotic to be used or treatment duration.
Although there are a few studies showing favorable results for use of nitrofurantoin during catheterization after pelvic surgery, there are no clearly defined recommendations regarding its use for urinary tract infection prevention after catheter removal. Therefore, the objective of our study is to examine the effects of administration of nitrofurantoin therapy at the time of Foley catheter removal for the prevention of catheter-associated UTI in patients undergoing POP and/or urinary incontinence surgery.
Primary Objective:
To evaluate the efficacy of administration of nitrofurantoin prophylaxis after catheter discontinuation for the prevention of catheter-associated urinary tract infections in patients with postoperative short-term catheterization following pelvic reconstructive surgery. The primary outcome will be the treatment of clinically suspected and/or culture-proven UTI within 30 days of surgery.
Secondary Objective:
To evaluate adverse outcomes related to study medications in each group and to evaluate medication compliance
Null Hypothesis:
The null hypothesis is that the administration of nitrofurantoin will not reduce the rate of UTI compared with placebo.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Catheter-Associated Urinary Tract Infection
Keywords
Nitrofurantoin, Prolapse, Pelvic Organ Prolapse, Anti-incontinence procedure, Urinary retention, Urinary Tract Infection, Short-term catheterization
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
164 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Nitrofurantoin
Arm Type
Active Comparator
Arm Description
Receives twice daily 100mg nitrofurantoin for 5 days following catheter removal
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Receives twice daily matching placebo for 5 days following catheter removal
Intervention Type
Drug
Intervention Name(s)
Nitrofurantoin 100 MG
Intervention Description
Patients will receive nitrofurantoin 100mg twice daily by mouth for 5 days
Intervention Type
Drug
Intervention Name(s)
Placebo Oral Tablet
Intervention Description
Matching placebo
Primary Outcome Measure Information:
Title
UTI
Description
Number of participants with a urinary tract infection in the first 30 days following pelvic reconstructive surgery
Time Frame
within 30 days of surgery
Secondary Outcome Measure Information:
Title
Adverse Events
Description
Number of participants with an adverse event only related to study drug administration
Time Frame
within 30 days of surgery
Title
Medication Compliance
Description
Compliance assessed by use of a medication diary during treatment period
Time Frame
within 30 days of surgery
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age greater than 18
Creatinine clearance greater than 30 ml/min
Failed postoperative hospital voiding trial
Exclusion Criteria:
Pregnant
History of glucose-6-phosphate dehydrogenase deficiency
History of renal insufficiency, renal transplant, or nephropathy
Allergy to nitrofurantoin
History of recurrent UTI (defined as greater than two culture-proven infections in six months or three infections in one year)
Urinary Tract Infection (UTI) within 14 days one month of surgery
Non-English speaking
Urinary tract infection while Foley catheter is in place
On antibiotic therapy for other non-urological reasons
Sustained intraoperative bladder injury requiring prolonged catheterization greater than 5 days
Undergoing mesh excision from within the bladder, fistula repair, cystotomy repair, urethral diverticulectomy, sacral neuromodulation, urethral surgery, or any other procedure requiring prolonged catheterization and bladder decompression
Placement of a suprapubic catheter
Participants that request intermittent self-catheterization
Neurologic conditions affecting urinary tract system and normal voiding mechanisms
History of hepatic impairment due to prior nitrofurantoin use
Inability to provide consent/decisionally impaired
More than two in-office voiding trials
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dina Bastawros, MD
Organizational Affiliation
Wake Forest University Health Sciences
Official's Role
Principal Investigator
Facility Information:
Facility Name
Atrium Health
City
Charlotte
State/Province
North Carolina
ZIP/Postal Code
28207
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
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Nitrofurantoin Administration for the Prevention of Short-Term Catheter Associated Urinary Tract Infection After Pelvic Surgery
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