Symptomatic Therapy of Uncomplicated Lower Urinary Tract Infections in the Ambulatory Setting.
Primary Purpose
Urinary Tract Infections
Status
Terminated
Phase
Phase 4
Locations
Switzerland
Study Type
Interventional
Intervention
Diclofenac
Norfloxacin
Sponsored by
About this trial
This is an interventional treatment trial for Urinary Tract Infections focused on measuring Urinary tract infections, Anti-bacterial agents
Eligibility Criteria
Inclusion Criteria:
- Female
- Age between 18 and 70 years
- Written informed consent
- At least one typical symptom of acute, lower urinary tract infection out of dysuria, frequency, macrohaematuria, cloudy or smelly urine or self-diagnosed cystitis
- A urine dipstick test should be indicative of UTI by positive nitrite or leucocyturia
Exclusion Criteria
- Duration of UTI symptoms for more than 7 days before physician's visit
- Clinical signs of invasiveness such as fever (axillary body temperature >38 degrees Celsius), costovertebral pain or tenderness, rigors, nausea or vomiting
- Known or suspicion of anatomical or functional abnormality of the urinary tract
- Vaginal symptoms: discharge, irritation
- Diabetes mellitus
- Immunosuppression (e.g. prednisone equivalent >10mg per day for >14 days, chemotherapy, radiotherapy, immunomodulators, HIV infection, neutropenia)
- Any other serious comorbidity as judged by the treating physician
- Bladder catheter in situ or during the past 30 days
- Pregnancy
- Recurrent urinary tract infection (more than 3 infections during the last 12 months)
- Antibiotic treatment during the last 4 weeks
- Hypersensitivity to one of the study medications
- Psychiatric illness or dementia
- Unable to communicate in German or French language
- Documented coagulopathy (including therapy with coumarine derivatives) or documented history of gastric or duodenal ulcer disease
- Documented renal insufficiency grade III or higher (calculated GFR <60) or known congestive heart failure (NYHA III or higher)
Sites / Locations
- Institute for Infectious Diseases, University of Berne
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
antibiotic
symptomatic
Arm Description
Norfloxacin for three days, followed by fosfomycin on day 4 if deemed necessary
Diclofenac retard for three days, followed by fosfomycin on day 4 if deemed necessary
Outcomes
Primary Outcome Measures
The proportion of patients with resolution of symptoms on day 4
Secondary Outcome Measures
The proportion of patients ever on antibiotics between randomization at day 1 and follow-up at day 30
The proportion of patients using single dose fosfomycin on day 4
The proportion of patients with re-consultations because of UTI within 30 days
The mean composite symptom scores on days 4, 7 and 30
The proportion of patients with resolution of symptoms on day 7
The proportion of patients with complete resolution of symptoms on days 4 and 7
The time until resolution of symptoms
The proportion of patients with adverse events
Mean overall patient stratification
Health-related quality of life on day 4
Number of working days lost
Full Information
NCT ID
NCT01039545
First Posted
December 24, 2009
Last Updated
July 8, 2015
Sponsor
Insel Gruppe AG, University Hospital Bern
Collaborators
University of Bern, Clinic for Infectious Diseases, University Hospital Bern, Switzerland
1. Study Identification
Unique Protocol Identification Number
NCT01039545
Brief Title
Symptomatic Therapy of Uncomplicated Lower Urinary Tract Infections in the Ambulatory Setting.
Official Title
Symptomatic Therapy of Uncomplicated Lower Urinary Tract Infections in the Ambulatory Setting. A Randomized, Double Blind Trial
Study Type
Interventional
2. Study Status
Record Verification Date
July 2015
Overall Recruitment Status
Terminated
Why Stopped
New power calculation (reduction of necessary patient number)
Study Start Date
February 2012 (undefined)
Primary Completion Date
December 2014 (Actual)
Study Completion Date
January 2015 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Insel Gruppe AG, University Hospital Bern
Collaborators
University of Bern, Clinic for Infectious Diseases, University Hospital Bern, Switzerland
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
We propose to perform a randomized controlled patient and assessor blind trial in women between the ages of 18 to 70 years with acute uncomplicated UTI to evaluate initial symptomatic treatment for 3 days with the non-steroidal anti-inflammatory drug diclofenac (experimental intervention) against immediate antibiotic treatment with norfloxacin for 3 days (control intervention). Both interventions are followed by optional delayed antibiotic treatment with single dose fosfomycin if deemed necessary by the patients. The primary objective is to determine whether initial symptomatic treatment followed by optional delayed antibiotic treatment (experimental intervention) is non-inferior to immediate antibiotic treatment (control intervention) in terms of symptom resolution.
Detailed Description
Background
Urinary tract infection (UTI) is the most frequent bacterial infection diagnosed and treated by general practitioners and accounts for about 15% of antibiotic prescriptions in ambulatory medicine. World-wide raise of antibiotic resistance among uropathogens, most commonly Escherichia coli, threatens treatment of UTI. Uncomplicated UTI, the most frequent manifestation of UTI, is a benign, self-limited disease and the primary goal of treatment is symptom relief not cure. Antibiotic treatment reduces the duration of symptoms by 1-2 days from 5-6 days to 3-4 days. Symptoms of cystitis are the result of an inflammation evoked by bacterial products which stimulate the production of prostaglandins by a cyclooxygenase dependent mechanism. Therefore, we propose that symptom control with a non-steroidal anti-inflammatory drug (NSAID), an inhibitor of cyclooxygenase 1 and 2, may be equally effective for symptom control as standard antibiotic therapy in non-complicated UTI and may therefore help to reduce antibiotic consumption.
Objective
The primary objective is to determine whether initial symptomatic treatment followed by optional delayed antibiotic treatment (experimental intervention) is non-inferior to immediate antibiotic treatment followed by optional delayed antibiotic treatment (control intervention) in terms of symptom resolution.
The secondary objective is to determine whether the experimental intervention is superior to control in reducing the proportion of patients undergoing antibiotic treatment.
Methods
Randomized controlled patient and assessor blind trial performed in general practices. Study population are women between the ages of 18 to 70 years with acute uncomplicated UTI. The experimental intervention will consist of symptomatic treatment with diclofenac 75mg twice daily, followed by optional, delayed antibiotic treatment with single dose of 3g fosfomycin if deemed necessary by the patient. The control intervention will consist of immediate antibiotic treatment with norfloxacin 400mg twice daily for three days, followed by optional, delayed antibiotic treatment with single dose of 3g fosfomycin if deemed necessary by the patient. Patients will use a diary to describe symptoms for 10 days. A follow-up telephone interview will be performed on day 10 and 30.
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, Anti-bacterial agents
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
253 (Actual)
8. Arms, Groups, and Interventions
Arm Title
antibiotic
Arm Type
Active Comparator
Arm Description
Norfloxacin for three days, followed by fosfomycin on day 4 if deemed necessary
Arm Title
symptomatic
Arm Type
Experimental
Arm Description
Diclofenac retard for three days, followed by fosfomycin on day 4 if deemed necessary
Intervention Type
Drug
Intervention Name(s)
Diclofenac
Intervention Description
Diclofenac retard 75mg twice daily for 3 days, followed by fosfomycin 3g single dose on day 4 if deemed necessary
Intervention Type
Drug
Intervention Name(s)
Norfloxacin
Intervention Description
Norfloxacin 400mg twice daily for 3 days, followed by fosfomycin 3g single dose on day 4 if deemed necessary
Primary Outcome Measure Information:
Title
The proportion of patients with resolution of symptoms on day 4
Time Frame
one month
Secondary Outcome Measure Information:
Title
The proportion of patients ever on antibiotics between randomization at day 1 and follow-up at day 30
Time Frame
one month
Title
The proportion of patients using single dose fosfomycin on day 4
Time Frame
one month
Title
The proportion of patients with re-consultations because of UTI within 30 days
Time Frame
one month
Title
The mean composite symptom scores on days 4, 7 and 30
Time Frame
one month
Title
The proportion of patients with resolution of symptoms on day 7
Time Frame
one month
Title
The proportion of patients with complete resolution of symptoms on days 4 and 7
Time Frame
one month
Title
The time until resolution of symptoms
Time Frame
one month
Title
The proportion of patients with adverse events
Time Frame
one month
Title
Mean overall patient stratification
Time Frame
one month
Title
Health-related quality of life on day 4
Time Frame
one month
Title
Number of working days lost
Time Frame
one month
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Female
Age between 18 and 70 years
Written informed consent
At least one typical symptom of acute, lower urinary tract infection out of dysuria, frequency, macrohaematuria, cloudy or smelly urine or self-diagnosed cystitis
A urine dipstick test should be indicative of UTI by positive nitrite or leucocyturia
Exclusion Criteria
Duration of UTI symptoms for more than 7 days before physician's visit
Clinical signs of invasiveness such as fever (axillary body temperature >38 degrees Celsius), costovertebral pain or tenderness, rigors, nausea or vomiting
Known or suspicion of anatomical or functional abnormality of the urinary tract
Vaginal symptoms: discharge, irritation
Diabetes mellitus
Immunosuppression (e.g. prednisone equivalent >10mg per day for >14 days, chemotherapy, radiotherapy, immunomodulators, HIV infection, neutropenia)
Any other serious comorbidity as judged by the treating physician
Bladder catheter in situ or during the past 30 days
Pregnancy
Recurrent urinary tract infection (more than 3 infections during the last 12 months)
Antibiotic treatment during the last 4 weeks
Hypersensitivity to one of the study medications
Psychiatric illness or dementia
Unable to communicate in German or French language
Documented coagulopathy (including therapy with coumarine derivatives) or documented history of gastric or duodenal ulcer disease
Documented renal insufficiency grade III or higher (calculated GFR <60) or known congestive heart failure (NYHA III or higher)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Andreas Kronenberg
Organizational Affiliation
University of Bern
Official's Role
Principal Investigator
Facility Information:
Facility Name
Institute for Infectious Diseases, University of Berne
City
Berne
ZIP/Postal Code
3010
Country
Switzerland
12. IPD Sharing Statement
Citations:
PubMed Identifier
29113968
Citation
Kronenberg A, Butikofer L, Odutayo A, Muhlemann K, da Costa BR, Battaglia M, Meli DN, Frey P, Limacher A, Reichenbach S, Juni P. Symptomatic treatment of uncomplicated lower urinary tract infections in the ambulatory setting: randomised, double blind trial. BMJ. 2017 Nov 7;359:j4784. doi: 10.1136/bmj.j4784. Erratum In: BMJ. 2017 Nov 13;359:j5268.
Results Reference
derived
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Symptomatic Therapy of Uncomplicated Lower Urinary Tract Infections in the Ambulatory Setting.
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