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Seven vs. 14 Days Treatment for Male Urinary Tract Infection

Primary Purpose

Urinary Tract Infections

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Longer therapy duration
Shorter therapy duration
Sponsored by
VA Office of Research and Development
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Urinary Tract Infections focused on measuring Urinary Tract Infections, Urinary antiinfective agents

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)MaleDoes not accept healthy volunteers

Inclusion Criteria:

Must have all

  • Male gender
  • New-onset (within 7 days) of at least one of the following symptoms/findings: dysuria, urinary frequency, urgency, hematuria, perineal pain, supra-pubic pain, costovertebral angle tenderness, or flank pain
  • Treated as an outpatient (Primary Care Center or Emergency Department), with < 24 hours observation in the hospital or Emergency Department following the time of initial diagnosis
  • Prescribed treatment with at least 7 days, but not more than 14 days, of either ciprofloxacin or TMP-SMZ

Exclusion Criteria:

Must have none

  • Admission to the hospital (for > 24h) at the time of diagnosis
  • Documented fever at time of initial evaluation ( 38.0 Celsius)
  • Previous enrollment in the study
  • Treatment for UTI in past 14 days
  • Not able to give informed consent
  • Unwilling to return for study visit
  • Symptoms thought more likely to be caused by a non-UTI diagnosis (e.g., urinary calculus, sexually transmitted infection, etc.)
  • Other antimicrobial therapy (new or ongoing) prescribed for a non-UTI diagnosis (e.g., cellulitis, pneumonia, etc.)
  • Treatment initiated with an empiric antimicrobial to which the organism isolated in the urine culture is non-susceptible based on standard laboratory criteria
  • Treatment initiated with an empiric antimicrobial regimen that is underdosed, based on current guidelines and reviews

Sites / Locations

  • Minneapolis VA Health Care System, Minneapolis, MN
  • Michael E. DeBakey VA Medical Center, Houston, TX

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Longer (14 day) duration antimicrobial treatment

Shorter (7 day) duration antimicrobial treatment

Arm Description

14 days of ciprofloxacin or trimethoprim/sulfamethoxazole

7 days of ciprofloxacin or trimethoprim/sulfamethoxazole, followed by 7 days of placebo

Outcomes

Primary Outcome Measures

Resolution of UTI Symptoms 14 Days After Completing Active Antimicrobial Therapy
This outcome will be assessed in a binary manner. Subjects with persistent UTI symptoms or having received further antimicrobials because of UTI symptoms will be considered to have not met the primary outcome, whereas those without persistent UTI symptoms and not having received further antimicrobials will be considered to have met the primary outcome.

Secondary Outcome Measures

Recurrent UTI Within 28 Days of Completing Active Study Medication
New onset of symptomatic UTI within the 28 day follow-up period
Adverse Drug Event in the 28 Days After Completing Study Medication
The incidence of adverse drug events, including nausea, vomiting, diarrhea, dizziness, headache, drug allergy, and C. difficile infection, both individually and in aggregate, will be compared between treatment groups This outcome is number of subjects experiencing ANY adverse drug event
Intestinal Carriage of Antimicrobial-resistant Gram Negative Bacilli
Intestinal carriage of antimicrobial-resistant Gram-negative bacilli after completing study medication, as compared to a baseline sample taken early in treatment. Antimicrobial resistance for this measure was defined as newly detected resistance to either of the study drugs, ciprofloxacin or trimethoprim/sulfamethoxazole.

Full Information

First Posted
November 19, 2013
Last Updated
May 13, 2021
Sponsor
VA Office of Research and Development
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1. Study Identification

Unique Protocol Identification Number
NCT01994538
Brief Title
Seven vs. 14 Days Treatment for Male Urinary Tract Infection
Official Title
Seven Versus Fourteen Day Treatment for Male Urinary Tract Infection
Study Type
Interventional

2. Study Status

Record Verification Date
May 2021
Overall Recruitment Status
Completed
Study Start Date
April 24, 2014 (Actual)
Primary Completion Date
December 31, 2019 (Actual)
Study Completion Date
December 31, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
VA Office of Research and Development

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study will investigate the treatment of urinary tract infection in men. Specifically, the investigators are looking to see if shorter duration of antibiotics (7 days) is any worse than longer duration of antibiotics (14 days). The investigators will also study whether longer treatment leads to an increase in antibiotic resistant bacteria in the large intestine (colon), or an increase in drug side effects.
Detailed Description
The proposed study is a randomized placebo-controlled trial of treatment duration for male urinary tract infection (UTI). Specifically, 319 men with a UTI will be randomized to 7 vs. 14 days of antimicrobial treatment. The primary outcome is resolution of UTI symptoms, assessed 14 days after completing active antimicrobial treatment. Secondary outcomes include recurrent UTI in the 4 weeks after treatment, adverse drug events, and intestinal carriage of antimicrobial resistant Gram-negative bacilli. Subjects will be enrolled from the Primary Care Clinic and Emergency Department at the Minneapolis VA Medical Center (MVAMC). Currently, the optimal treatment duration for male UTI is unknown. A clinical trial of 14 vs. 28 days of treatment showed no difference in outcomes, whereas another trial of 3 vs.14 days showed an increase in recurrence with 3 days of treatment. However, current treatment recommendations are to treat men with UTI for 7 to 14 days, and no data exist to favor the shorter or longer duration. Most men with UTI in the VA are treated for more than 7 days, which is associated with a small but significant increase in Clostridium difficile infection. Additionally, other studies of non-UTI infectious diseases have shown that longer-duration treatment leads to increased antimicrobial resistance. Longer-duration treatment is also more costly and inconvenient to patients. Thus, since longer-duration treatment is associated with some adverse outcomes, in order to justify longer-duration treatment thee must be some clinically significant benefit to the extended treatment. Accordingly, the proposed randomized placebo-controlled trial of 319 men with UTI will test the hypothesis that 7 days of antimicrobial treatment is non-inferior for the resolution of UTI symptoms when compared to 14 days of treatment. This study will provide valuable information to VA patients and clinicians regarding a common and understudied clinical decision.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Urinary Tract Infections
Keywords
Urinary Tract Infections, Urinary antiinfective agents

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
273 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Longer (14 day) duration antimicrobial treatment
Arm Type
Active Comparator
Arm Description
14 days of ciprofloxacin or trimethoprim/sulfamethoxazole
Arm Title
Shorter (7 day) duration antimicrobial treatment
Arm Type
Placebo Comparator
Arm Description
7 days of ciprofloxacin or trimethoprim/sulfamethoxazole, followed by 7 days of placebo
Intervention Type
Other
Intervention Name(s)
Longer therapy duration
Intervention Description
14 days of antimicrobial treatment
Intervention Type
Other
Intervention Name(s)
Shorter therapy duration
Intervention Description
7 days of antimicrobial treatment
Primary Outcome Measure Information:
Title
Resolution of UTI Symptoms 14 Days After Completing Active Antimicrobial Therapy
Description
This outcome will be assessed in a binary manner. Subjects with persistent UTI symptoms or having received further antimicrobials because of UTI symptoms will be considered to have not met the primary outcome, whereas those without persistent UTI symptoms and not having received further antimicrobials will be considered to have met the primary outcome.
Time Frame
14 days
Secondary Outcome Measure Information:
Title
Recurrent UTI Within 28 Days of Completing Active Study Medication
Description
New onset of symptomatic UTI within the 28 day follow-up period
Time Frame
28 days
Title
Adverse Drug Event in the 28 Days After Completing Study Medication
Description
The incidence of adverse drug events, including nausea, vomiting, diarrhea, dizziness, headache, drug allergy, and C. difficile infection, both individually and in aggregate, will be compared between treatment groups This outcome is number of subjects experiencing ANY adverse drug event
Time Frame
28 days
Title
Intestinal Carriage of Antimicrobial-resistant Gram Negative Bacilli
Description
Intestinal carriage of antimicrobial-resistant Gram-negative bacilli after completing study medication, as compared to a baseline sample taken early in treatment. Antimicrobial resistance for this measure was defined as newly detected resistance to either of the study drugs, ciprofloxacin or trimethoprim/sulfamethoxazole.
Time Frame
7 days

10. Eligibility

Sex
Male
Gender Based
Yes
Gender Eligibility Description
Study of UTI in men
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Must have all Male gender New-onset (within 7 days) of at least one of the following symptoms/findings: dysuria, urinary frequency, urgency, hematuria, perineal pain, supra-pubic pain, costovertebral angle tenderness, or flank pain Treated as an outpatient (Primary Care Center or Emergency Department), with < 24 hours observation in the hospital or Emergency Department following the time of initial diagnosis Prescribed treatment with at least 7 days, but not more than 14 days, of either ciprofloxacin or TMP-SMZ Exclusion Criteria: Must have none Admission to the hospital (for > 24h) at the time of diagnosis Documented fever at time of initial evaluation ( 38.0 Celsius) Previous enrollment in the study Treatment for UTI in past 14 days Not able to give informed consent Unwilling to return for study visit Symptoms thought more likely to be caused by a non-UTI diagnosis (e.g., urinary calculus, sexually transmitted infection, etc.) Other antimicrobial therapy (new or ongoing) prescribed for a non-UTI diagnosis (e.g., cellulitis, pneumonia, etc.) Treatment initiated with an empiric antimicrobial to which the organism isolated in the urine culture is non-susceptible based on standard laboratory criteria Treatment initiated with an empiric antimicrobial regimen that is underdosed, based on current guidelines and reviews
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dimitri M Drekonja, MD
Organizational Affiliation
Minneapolis VA Health Care System, Minneapolis, MN
Official's Role
Principal Investigator
Facility Information:
Facility Name
Minneapolis VA Health Care System, Minneapolis, MN
City
Minneapolis
State/Province
Minnesota
ZIP/Postal Code
55417
Country
United States
Facility Name
Michael E. DeBakey VA Medical Center, Houston, TX
City
Houston
State/Province
Texas
ZIP/Postal Code
77030
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
No formal plan submitted at time of grant. Will handle such requests on a case-by-case basis with input from local privacy officer and institutional review board.
IPD Sharing Time Frame
Anticipate will share data for 2 years after publication of the primary result manuscript
IPD Sharing Access Criteria
Requests will be handled on a case-by-case basis with input from the local privacy officer and IRB.
Citations:
PubMed Identifier
34313686
Citation
Drekonja DM, Trautner B, Amundson C, Kuskowski M, Johnson JR. Effect of 7 vs 14 Days of Antibiotic Therapy on Resolution of Symptoms Among Afebrile Men With Urinary Tract Infection: A Randomized Clinical Trial. JAMA. 2021 Jul 27;326(4):324-331. doi: 10.1001/jama.2021.9899.
Results Reference
derived

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Seven vs. 14 Days Treatment for Male Urinary Tract Infection

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