Recurrent urinary tract infection in women MedDRA version: 18.1 Level: PT Classification code 10064736 Term: Antibiotic prophylaxis System Organ Class: 10042613 - Surgical and medical procedures
Conditions
Interventions
Trade Name: Hiprex
Product Name: methenamine hippurate
Pharmaceutical Form: Tablet
INN or Proposed INN: Methenamine Hippurate
CAS Number: 5714-73-8
Concentration unit: g gram(s)
Concentration type: eq
Sponsors
The Newcastle upon Tyne Hospitals NHS Foundation Trust
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: • Women aged 18 years and over. • Women with rUTI who, in consultation with a clinician, have decided that prophylaxis is an appropriate option (to include women who have suffered at least three episodes of symptomatic UTI within the preceding 12 months or two episodes in the last 6 months or a single severe infection requiring hospitalisation). • Able to take a once daily oral dose of at least one of nitrofurantoin, or trimethoprim, or cephalexin. • Able to take Methenamine hippurate. • Women who agree to take part in the trial but who are already taking Methenamine or antibiotic prophylaxis will be consented for participation and will stop their preventative therapy for a 3-month washout period. They will then be reassessed and if still eligible undergo baseline assessment and randomisation. • Able to give informed consent for participation in trial. • Able and willing to adhere to an 18-month study period. Are the trial subjects under 18? no Number of subjects for this age range: 0 F.1.2 Adults (18-64 years) yes F.1.2.1 Number of subjects for this age range 200 F.1.3 Elderly (>=65 years) yes F.1.3.1 Number of subjects for this age range 40
Exclusion criteria
Exclusion criteria: • Women unable to take Methenamine hippurate e.g. known allergy to Methenamine hippurate, severe hepatic impairment (Childs –Pugh class C, score of 10 or more, see appendix 4), gout, eGFR < 10 ml/min, Proteus sp. as consistent proven causative organism for rUTIs. • Women who are unable to take nitrofurantoin and trimethoprim and cephalexin. • Women with correctable urinary tract abnormalities that are considered to be contributory to the occurrence of rUTI. • Presence of symptomatic UTI – this will be treated and symptoms resolved prior to randomisation. • Pregnancy or intended pregnancy in next 12 months. • Women who are breast feeding. • Women already taking methenamine or antibiotic prophylaxis and declining a 3-month washout period.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Main Objective: Our principal research questions are: Is a twice daily dose of Methenamine Hippurate at least as effective as low dose prophylactic antibiotics in offering symptomatic relief to women with recurrent Urinary Tract Infection (rUTI)? This is reported by comparing the number of symptomatic episodes of rUTI by women in each trial group over a 12 month treatment period. We are also trying to determine whether the use of Methanamine Hippurate is no worse in terms of value for money to the NHS than the use of prophylactic antibiotics over the 12 months.;Secondary Objective: To determine the number of symptomatic antibiotic-treated UTI self-reported by patients during the 6 month period after completion of allocated treatment. To determine the total number of days spent on urinary specific antibiotics (prophylactic or treatment) during 12 month active study period and six month follow up. To determine if there is any ecological change in bacteria and their resistance patterns in samples taken from participant’s i) urine and ii) faecal reservoir during the 12 month treatment period and in the 6 months following completion of treatment. To determine the number of microbiologically proven urinary tract infections during the 12 month treatment and 6 month follow-up periods. To determine the incidence of asymptomatic bacteriuria (ABU) during the study period. To determine the rate of hospitalization due to urinary tract infections during the study period. To determine overall patients satisfaction with antibiotic versus antiseptic treatment. ;Primary end point(s): The Primary clinical outcome is the incidence of symptomatic antibiotic-treated UTI self-reported by participants over the 12-month treatment period. This will be defined as the presence of at least one patient-reported or clinician-recorded symptom from a predefined list encompassing the recommendations of the British Infection Association (BIA) together with taking a discrete treatment course of | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary end point(s): The number of symptomatic antibiotic-treated UTI self-reported by participants in the 6 months follow up period after completing the allocated preventative therapy. Total antibiotic use during the study period, reported by patients and verified where necessary from medical records. Phenotype and genotype of Escherichia coli (E. coli) isolated from urine and perineal swabs sent by participants directly to the central reference laboratory. The number of microbiologically confirmed urinary tract infections occurring during both the 12 months of treatment and the subsequent 6 months of follow-up . A positive culture will be classified according to standard Public Health England (PHE) definitions; the laboratory report of two isolates at = 105 cfu/mL or a single isolate at = 104 cfu/mL. Presence of asymptomatic bacteriuria (ABU) identified by urine culture performed at patient visits for study follow-up. ABU is defined as the presence of bacteria in the urine in the absence of symptoms suggestive of urinary tract infection. For the purposes of this study, a positive culture was defined in line with the routine PHE definitions above. The rate of hospitalisation due to urinary tract infections during the treatment and follow-up phases of the study. Overall satisfaction with treatment measured by Treatment Questionnaire on Satisfaction with Medication (TQSM) administered at both the end of treatment (12 months) and then again at the end of follow-up (18 months). Qualitative analysis of patients and clinicians views regarding trial processes and participation. QALYs based on responses to the EQ-5D -5L at 3, 6, 9, 12, 15 and 18 months and after a UTI episode. Treatment costs for drug and healthcare services from a standard NHS source such as British Formulary (BNF) and published tariffs from NHS reference costs. Health resource utilisation questionnaire at 3,6, 9, 12,15 and 18 months. Incremental cost per quality-adjusted life year (QALY) | — |
Countries
United Kingdom
Contacts
Public ContactChris Harding
Freeman Hospital
Outcome results
None listed