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Fractional CO2 Vaginal LASER Therapy for Recurrent Urinary Tract Infection

Primary Purpose

Urinary Tract Infections

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Mona Lisa Touch
Conjugated estrogen
Estradiol
Sponsored by
Mayo Clinic
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Urinary Tract Infections

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Female patient >18 years old
  • Postmenopausal status, documented by prior bilateral salpingo-oophorectomy, or absence of menses >12 months
  • Recurrent urinary tract infections as defined by 3 culture positive urine cultures in the last 12 months, or 2 positive urine cultures in the last 6 months.(Positive urine cultures defined by >100K colony forming units of 1 or 2 bacterial species on clean catch sample, or >1000 colony forming units of 1 or 2 bacterial species on sample via straight catheterization).
  • Patients on vaginal estrogen must undergo a 1 month washout period prior to initiation of the trial.

Exclusion Criteria:

  • Hematuria without appropriate workup
  • Pelvic organ prolapse at or beyond the hymen
  • Clinically relevant urinary retention
  • Pelvic reconstructive surgery within 6 months
  • Prior synthetic mesh procedure for pelvic organ prolapse or urinary incontinence
  • Clinically relevant nephrolithiasis
  • History of breast cancer
  • Contraindication to topical estrogen therapy
  • Anticoagulation therapy
  • Prior pelvic or vaginal radiation therapy
  • Prior gynecologic malignancy
  • Undiagnosed genital bleeding

Sites / Locations

  • Mayo Clinic in Arizona

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Vaginal Estrogen Therapy Group

Laser Therapy Group

Arm Description

Women randomized to vaginal estrogen therapy will be offered vaginal cream conjugated estrogen (Premarin) 0.5 gm per vaginal twice weekly or estradiol (Estrace): 1gm per vaginal twice weekly

Women randomized to the laser therapy group will undergo 3 treatments, 6 weeks apart.

Outcomes

Primary Outcome Measures

Improvement in recurrence of culture positive urinary tract infections
Number of culture positive, symptomatic urinary tract infections in women

Secondary Outcome Measures

Full Information

First Posted
March 6, 2020
Last Updated
May 30, 2023
Sponsor
Mayo Clinic
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1. Study Identification

Unique Protocol Identification Number
NCT04301934
Brief Title
Fractional CO2 Vaginal LASER Therapy for Recurrent Urinary Tract Infection
Official Title
Fractional CO2 Vaginal LASER Therapy for Recurrent Urinary Tract Infection
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Completed
Study Start Date
June 1, 2020 (Actual)
Primary Completion Date
April 30, 2023 (Actual)
Study Completion Date
April 30, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Mayo Clinic

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Data Monitoring Committee
No

5. Study Description

Brief Summary
Randomized controlled trial to determine clinical and microbiome difference between fractional CO2 Laser and vaginal estrogen in treating patients with recurrent urinary tract infection (UTI).
Detailed Description
Recurrent urinary tract infection (rUTI) is common in postmenopausal women and can lead to significant bothersome symptoms. This clinical scenario is a difficult and common clinical problem seen by the urologist and urogynecologist with limited options for treatment. Overuse of antibiotics has led to significant resistant microorganisms and can have adverse side effects such as C. Dificile colitis. Current treatments include topical vaginal estrogen and prophylactic antibiotics. Other supplements such as cranberry pills, methenamine and D-mannose have varying levels of evidence and efficacy. Fractional CO2 LASER vaginal therapy has recently been studied for the treatment of GSM. LASER therapy is currently commercially available and has FDA clearance for use in gynecology. Current evidence shows that with treatment, histologic changes of the vaginal epithelium have shown regeneration to a premenopausal state, along with subjective improvement in GSM symptoms and sexual function. Recent literature has shown improvements in thickening of vaginal epithelium, decreased vaginal pH and improvement in the vaginal microbiome. Based on this, the investigators propose fractional CO2 laser may have a positive impact on women with rUTI. The investigators therefore hypothesize that fractional CO2 LASER vaginal therapy is non-inferior to topical vaginal estrogen therapy for the treatment of rUTI. a. Primary Outcome: Improvement in recurrence of culture positive UTI The investigators also hypothesize that LASER therapy will improve the urinary and vaginal microbiome, decreasing the uropathogenic presence and increasing Lactobacillus. Measurement 1: The number of UTI with UPEC isolated from patients Measurement 2: The pH of the vagina as a proxy for presence of Lactobacillus sp. Measurement 3: Categorize vaginal and urinary microbial communities The investigators hypothesize that LASER therapy will improve symptoms of GSM and be associated with regenerative change in vaginal histology. Measurement 1: MESA and DIVA surveys of symptoms Measurement 2: Observations of vaginal biopsy between. Menopausal women will be recruited if subjects have recurrent UTI defined as 3 culture positive UTIs in 1 year or 2 culture positive UTIs in 6 months. Subjects will be randomized to standard of care with topical vaginal estrogen or 3 treatments of fractional CO2 LASER of the vagina. Samples will be collected to show microbiome and histologic changes with treatment. Samples include: Vaginal culture Urine culture vaginal biopsy (optional). Validated questionnaires and clinical recurrence of UTI will also be gathered over 6 months.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Urinary Tract Infections

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
12 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Vaginal Estrogen Therapy Group
Arm Type
Active Comparator
Arm Description
Women randomized to vaginal estrogen therapy will be offered vaginal cream conjugated estrogen (Premarin) 0.5 gm per vaginal twice weekly or estradiol (Estrace): 1gm per vaginal twice weekly
Arm Title
Laser Therapy Group
Arm Type
Experimental
Arm Description
Women randomized to the laser therapy group will undergo 3 treatments, 6 weeks apart.
Intervention Type
Device
Intervention Name(s)
Mona Lisa Touch
Intervention Description
Fractional CO2 LASER
Intervention Type
Drug
Intervention Name(s)
Conjugated estrogen
Other Intervention Name(s)
Premarin
Intervention Description
Current standard treatment for recurrent UTIs in postmenopausal women
Intervention Type
Drug
Intervention Name(s)
Estradiol
Other Intervention Name(s)
Estrace
Intervention Description
Current standard treatment for recurrent UTIs in postmenopausal women
Primary Outcome Measure Information:
Title
Improvement in recurrence of culture positive urinary tract infections
Description
Number of culture positive, symptomatic urinary tract infections in women
Time Frame
6 months

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Female patient >18 years old Postmenopausal status, documented by prior bilateral salpingo-oophorectomy, or absence of menses >12 months Recurrent urinary tract infections as defined by 3 culture positive urine cultures in the last 12 months, or 2 positive urine cultures in the last 6 months.(Positive urine cultures defined by >100K colony forming units of 1 or 2 bacterial species on clean catch sample, or >1000 colony forming units of 1 or 2 bacterial species on sample via straight catheterization). Patients on vaginal estrogen must undergo a 1 month washout period prior to initiation of the trial. Exclusion Criteria: Hematuria without appropriate workup Pelvic organ prolapse at or beyond the hymen Clinically relevant urinary retention Pelvic reconstructive surgery within 6 months Prior synthetic mesh procedure for pelvic organ prolapse or urinary incontinence Clinically relevant nephrolithiasis History of breast cancer Contraindication to topical estrogen therapy Anticoagulation therapy Prior pelvic or vaginal radiation therapy Prior gynecologic malignancy Undiagnosed genital bleeding
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Johnny Yi, MD
Organizational Affiliation
Mayo Clinic
Official's Role
Principal Investigator
Facility Information:
Facility Name
Mayo Clinic in Arizona
City
Phoenix
State/Province
Arizona
ZIP/Postal Code
85054
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Links:
URL
https://www.mayo.edu/research/clinical-trials
Description
Mayo Clinic Clinical Trials

Learn more about this trial

Fractional CO2 Vaginal LASER Therapy for Recurrent Urinary Tract Infection

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