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Clinical Trials/NCT06124820
NCT06124820
Active, not recruiting
Not Applicable

A Single-blinded, Randomised Controlled Trial Comparing the Use of Intravaginal Laser Therapy to Sham in Post-menopausal Women with Recurrent Urinary Tract Infections (rUTI) and the Impact on the Vaginal and Urinary Microbiome

King's College Hospital NHS Trust1 site in 1 country48 target enrollmentOctober 1, 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Recurrent Urinary Tract Infection
Sponsor
King's College Hospital NHS Trust
Enrollment
48
Locations
1
Primary Endpoint
To determine and compare the incidence of symptomatic antibiotic-treated UTI during the 6-month follow-up period after completion of allocated treatment
Status
Active, not recruiting
Last Updated
last year

Overview

Brief Summary

Recurrent urinary tract infection (rUTI) is a common and difficult to treat problem with limited treatment option; postmenopausal women are disproportionately affected. The genitourinary syndrome of menopause (GSM) describes the broad spectrum of signs and symptoms caused by the loss of endogenous sex steroids. The combined effects of urogenital epithelial tissue thinning and changes to the vaginal and bladder microbiome can predispose to ascending UTIs. Recurrent UTIs is a component of GSM.

Intravaginal laser therapy has been shown to be safe and effective for the treatment of GSM, however, the role of laser for treatment of recurrent UTIs is unknown. We hypothesis that the incidence of UTI will be reduced as CO2 laser restores vaginal epithelium to a state similar to that of a pre-menopausal woman, preventing microtrauma, and increases Lactobacillus and normal flora (Athanasiou et al., 2016). Lactobacillus is considered the bacteria that helps keep the vagina healthy and infection free through its production of lactic acid which lowers vaginal pH, this more acidic environment may be protective from uropathogens.

We therefore aim to conduct a single-blinded, multi-centre, randomised controlled trial comparing the use of intravaginal CO2 laser therapy to sham in post-menopausal women with rUTIs and to determine the impact on the microbiome.

Detailed Description

Urinary tract infections (UTIs) are the most common outpatient infection with a prevalence of 20% in women over 65, compared with 11% in the overall population (Chu and Lowder, 2018). The genitourinary syndrome of menopause (GSM) is the accepted term used to describe the broad spectrum of genitourinary tract symptoms and signs caused by the loss of endogenous sex steroids that occurs at the time of and after the menopause. Global improvements in healthcare have resulted in an aging population. Today women are spending 40% of their lives in the postmenopausal state with 50-70% of postmenopausal women reporting symptomatic GSM. The combined effects of urogenital epithelial tissue thinning and changes to the vaginal and bladder microbiome can predispose to ascending UTIs. Recurrent UTIs is a component of GSM. Current interventions for recurrent urinary tract infections in women include lifestyle and behavioural advice, complimentary therapies and antibiotics. These treatment regimens are not always effective or acceptable. Intravaginal Laser therapy is an alternative non-hormonal treatment of GSM as it stimulates tissue repair and restores normal vaginal function. Currently intravaginal laser therapy has been shown to be safe and effective for the treatment of GSM, as described in a recent network analysis of 29 randomised controlled studies, incorporating 8311 patients (Li et al., 2021). Provisional results using FemTouch®, fractional CO2 laser, appear promising with 9/12 (75%) of post-menopausal women UTI free at 12 months follow-up (Yang and Foley). However, there is a scarcity of studies available looking at the impact of this novel technology for the treatment of recurrent UTIs. The investigators aim to conduct a single-blinded, randomised controlled trial comparing the use of intravaginal CO2 laser therapy to sham in post-menopausal women with rUTIs and to determine the impact on the microbiome. The investigators hypothesise that this treatment will be effective in reducing the incidence of urinary tract infection as CO2 laser through a process of thermomodulation, simulates tissue repair by restoring vaginal epithelium to a state similar to that of a pre-menopausal woman. In addition, a study assessing the effect of micro-ablative functional CO2 laser reported an increase in Lactobacillus and normal flora (Athanasiou et al., 2016). Lactobacillus is considered the bacteria that helps keep the vagina healthy and infection free through its production of lactic acid which lowers the vaginal pH, this more acidic environment may be protective from uropathogens. The role and impact of Laser on other microbial communities is still not fully understood, this study aims to expand this knowledge base. Recurrent UTIs is a common and difficult to treat problem with limited treatment options, this study endeavors to expand the knowledge pool and provide alternative non-pharmacological options using this novel technology.

Registry
clinicaltrials.gov
Start Date
October 1, 2023
End Date
October 8, 2026
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Sponsor
King's College Hospital NHS Trust
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Postmenopausal women
  • History of recurrent UTI (Defined as women who have suffered at least three episodes of symptomatic UTI within the preceding 12 months or two episodes in the last six months, or at least one episode of UTI requiring hospitalisation, or if previously prescribed prophylactic antibiotics for UTI, have completed a 3-month washout period without antibiotic prophylaxis)
  • Able to give informed consent for participation in the trial
  • Able and willing to adhere to a 17-month study period

Exclusion Criteria

  • Not willing to abstain from vaginal intercourse for 48 hours following laser-therapy
  • Use of vaginal hormonal therapy in the three months before study start
  • History of a genital fistula, a thin recto-vaginal septum as determined by the investigator or history of a fourth-degree laceration during physical screening exam (e.g., deficient perineal body)
  • Active sexually transmitted disease upon vaginal exam (as determined by the investigator) that precludes treatment or any other vaginal infection
  • History of lichen sclerosis
  • History of radiotherapy for cervical or uterine cancer
  • A medical condition that may interfere with participants' compliance with the protocol
  • Women with correctable urinary tract abnormalities that are considered to be contributory to the occurrence of rUTI
  • Women taking Methenamine Hippurate and unable to undergo a three-month washout period
  • Undiagnosed genital bleeding

Outcomes

Primary Outcomes

To determine and compare the incidence of symptomatic antibiotic-treated UTI during the 6-month follow-up period after completion of allocated treatment

Time Frame: 6 months

Determined from the UTI history diary and cross-referenced with hospital and GP records

Secondary Outcomes

  • Vaginal Health Index Score (VHIS)(18 months)
  • King's Health Questionnaire (KHQ)(18 months)
  • 16S rRNA rapid Next-generation Gene Sequencing(18 months)
  • Dipstick urine analysis(18 months)
  • Vulvoscopic Genital Tissue Appearance Scale (VGTA)(18 months)
  • Expanded Quantitative Urine Culture (EQUC)(18 months)
  • Shotgun metagenomic sequencing(18 months)
  • UTI history diary(18 months)
  • International Consultation on Incontinence Questionnaire - Vaginal Symptoms (ICIQ-VS)(18 months)
  • Urinary Tract Infection Symptom Assessment Questionnaire (UTISA)(18 months)
  • International Consultation on Incontinence Questionnaire - Female Lower Urinary Tract Symptoms (ICIQ-FLUTS)(18 months)
  • 10 cm Visual Analogue Scale for Symptoms (VAS)(18 months)
  • Health Service Utilisation Questionnaire (HSU-Q)(18 months)
  • Treatment satisfaction questionnaire for laser (TSQ-L)(18 months)
  • Adverse event recording(18 months)
  • Female Sexual Function Index Scoring (FSFI)(18 months)
  • Standard urine culture(18 months)

Study Sites (1)

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