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NCT Number: NCT06124820

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

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.

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This study is active but is not currently recruiting participants.

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Key information

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

King's College Hospital

London, SE5 9RS, United Kingdom

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Deka SmartXide Touch C60 (MonaLisa Touch)

Device

Intravaginal micro-ablative fractional CO2 laser technology Deka SmartXide Touch C60 (MonaLisa Touch)

SHAM

Device

Participants receiving sham treatment will have the probes advanced in the same manner without the use of a laser energy device.

Primary outcomes

  1. 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

  1. UTI history diary

    Time frame: 18 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.

  2. Vaginal Health Index Score (VHIS)

    Time frame: 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.

  3. King's Health Questionnaire (KHQ)

    Time frame: 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).

  4. International Consultation on Incontinence Questionnaire - Female Lower Urinary Tract Symptoms (ICIQ-FLUTS)

    Time frame: 18 months

    A 12 item questionnaire for evaluating female lower urinary tract symptoms

  5. International Consultation on Incontinence Questionnaire - Vaginal Symptoms (ICIQ-VS)

    Time frame: 18 months

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

  6. 10 cm Visual Analogue Scale for Symptoms (VAS)

    Time frame: 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

  7. Urinary Tract Infection Symptom Assessment Questionnaire (UTISA)

    Time frame: 18 months

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

  8. Female Sexual Function Index Scoring (FSFI)

    Time frame: 18 months

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

  9. Health Service Utilisation Questionnaire (HSU-Q)

    Time frame: 18 months

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

  10. Treatment satisfaction questionnaire for laser (TSQ-L)

    Time frame: 18 months

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

  11. Vulvoscopic Genital Tissue Appearance Scale (VGTA)

    Time frame: 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

  12. Adverse event recording

    Time frame: 18 months

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

  13. Dipstick urine analysis

    Time frame: 18 months

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

  14. Standard urine culture

    Time frame: 18 months

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

  15. Expanded Quantitative Urine Culture (EQUC)

    Time frame: 18 months

    • EQUC uses larger urine volume, longer incubation times, multiple growth media and atmospheric conditions and enables species-level identification
  16. 16S rRNA rapid Next-generation Gene Sequencing

    Time frame: 18 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

  17. Shotgun metagenomic sequencing

    Time frame: 18 months

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

Sponsors and collaborators

Lead sponsor

King's College Hospital NHS Trust

Other

Registry information

Official study title

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

Acronym: UTIEXTERMINATE

Important dates

Study start
2023
Primary completion
2026
Study completion
2026
First posted
Nov 9, 2023
Registry last updated
Mar 10, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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