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RCT Comparing Intravaginal Laser Therapy to Sham in Post-menopausal Women with Recurrent Urinary Tract Infections

Not Applicable
Active, not recruiting
Conditions
Recurrent Urinary Tract Infection
Genitourinary Syndrome of Menopause
Interventions
Device: Deka SmartXide Touch C60 (MonaLisa Touch)
Device: Sham
Registration Number
NCT06124820
Lead Sponsor
King's College Hospital NHS Trust
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.

Recruitment & Eligibility

Status
ACTIVE_NOT_RECRUITING
Sex
Female
Target Recruitment
48
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
  • Women who self-catheterise, or have an indwelling/suprapubic catheter
  • Unable to give informed consent

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Treatment ArmDeka SmartXide Touch C60 (MonaLisa Touch)Intravaginal micro-ablative fractional CO2 laser technology Deka SmartXide Touch C60 (MonaLisa Touch) will be administered intravaginally over a course of 5 cycles
Control ArmShamSham treatment -Participants receiving sham treatment will have the probes advanced in the same manner without the use of a laser energy device.
Primary Outcome Measures
NameTimeMethod
To determine and compare the incidence of symptomatic antibiotic-treated UTI during the 6-month follow-up period after completion of allocated treatment6 months

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

Secondary Outcome Measures
NameTimeMethod
Vaginal Health Index Score (VHIS)18 months

o It incorporates a clinical examination of the vagina for pH, elasticity, fluid volume, epithelial integrity, moisture. Vaginal pH will be obtained using a piece of litmus paper placed on the lateral wall of the vagina.

King's Health Questionnaire (KHQ)18 months

21 items about urinary tract symptoms yield scores in 9 domains (general health perception, incontinence impact, role limitations, physical limitations, social limitations, personal relationships, emotions, sleep/energy \& severity of symptoms).

Dipstick urine analysis18 months

Reagent strips used to detect substances in urine including nitrate, leucocytes, glucose, protein, pH, ketones and blood

16S rRNA rapid Next-generation Gene Sequencing18 months

16S rRNA NGS provide gene-level information for species. It utilises PCR amplification and NGS of essential 16S ribosomal RNA genes. It enables the evaluation of even closely related bacterial species through evolutionary polymorphisms

Vulvoscopic Genital Tissue Appearance Scale (VGTA)18 months

assesses 10 parameters of the appearance of the genital tissue including loss of labia minora/majora, decreased glans clitoris, stenosis of introitus, prominence of the urethral meatus, vestibular pallor, vestibular pallor, vesicular erythema, loss of vaginal rugae, loss of vestibular moisture and loss of prominence of the anterior vaginal wall. A score of 0 to 30 is obtained, the higher the score the worse the vulvoscopic genital tissue appearance

Expanded Quantitative Urine Culture (EQUC)18 months

- EQUC uses larger urine volume, longer incubation times, multiple growth media and atmospheric conditions and enables species-level identification

Shotgun metagenomic sequencing18 months

allows the identification and profiling of microbial species independent of reference sequences.

UTI history diary18 months

Participants will be given a UTI history diary to complete which will documents all symptomatic and treated UTI, the diary will be cross-referenced with participant history and review of medical history at each follow-up appointment.

International Consultation on Incontinence Questionnaire - Vaginal Symptoms (ICIQ-VS)18 months

A 14 item questionnaire for evaluating vaginal symptoms, associated sexual matters and impact on quality of life (QoL)

Urinary Tract Infection Symptom Assessment Questionnaire (UTISA)18 months

14-item questionnaire asking about the severity and bothersome of seven key UTI symptoms.

International Consultation on Incontinence Questionnaire - Female Lower Urinary Tract Symptoms (ICIQ-FLUTS)18 months

A 12 item questionnaire for evaluating female lower urinary tract symptoms

10 cm Visual Analogue Scale for Symptoms (VAS)18 months

Consists of a 10cm line, used to determine intensity of symptoms with two endpoints representing 0 ("no symptoms" and 10 ("symptom at the worse it could be"). Symptoms assessed: vaginal dryness, dyspareunia, itching, burning, dysuria, frequency, urgency, overall symptoms

Health Service Utilisation Questionnaire (HSU-Q)18 months

An instrument for the standardized and systematic assessment of various aspects of health care utilisation

Treatment satisfaction questionnaire for laser (TSQ-L)18 months

A modified 10-item questionnaire used to determine participant satisfaction with treatment

Adverse event recording18 months

Adverse events will be asked at each visit and participant will have contact details to reports any throughout the study period

Female Sexual Function Index Scoring (FSFI)18 months

A 19 item questionnaire designed to measure sexual functioning in women.

Standard urine culture18 months

Routine urinalysis that identify bacteria or yeast causing a urinary tract infection

Trial Locations

Locations (1)

King's College Hospital

🇬🇧

London, United Kingdom

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