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Comparative Study: Vaginal Promestriene Use, Fractional CO2 LASER and Radiofrequency in the Vaginal Atrophy Treatment

Primary Purpose

Vaginal Atrophy

Status
Completed
Phase
Not Applicable
Locations
Brazil
Study Type
Interventional
Intervention
Promestriene Vaginal
Fractional CO2 LASER
Microablative Fractional radiofrequency
Sponsored by
University of Sao Paulo General Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Vaginal Atrophy focused on measuring genital atrophy, fractional CO2 laser, microablative fractional radiofrequency, quality of life, sexuality, promestriene, Menopause genitourinary syndrome

Eligibility Criteria

40 Years - 65 Years (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

Age equal or superior to 40 years and under 65 years

  • Clinical menopause - last menstrual period from 1 to 5 years from the date of recruitment
  • FSH measurement> 25 IU / ml, estrogen <20 æg / ml
  • Patients with vaginal atrophy and clinical and / or sexual symptoms
  • Patients without hormonal treatment for at least five years

Exclusion Criteria:

  • Whole Hymen

    • Altered oncology cytology of the cervix and / or vagina
    • Vaginal infections
    • Connective tissue diseases
    • Immunosuppression
    • Coagulation change
    • Diabetes Mellitus
    • Thyroid diseases
    • Use of systemic or local feminine hormones
    • Use of other substances with estrogenic properties

Sites / Locations

  • Disciplina de ginecologia - departamento de ginecologia e obstetrícia - faculdade de medicina da USP

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

Active Comparator

Arm Label

Fractional CO2 LASER

Microablative fractional radiofrequency

Promestriene Vaginal

Arm Description

Vaginal fractional CO2 LASER 3 sessions applications

Vaginal Microablative fractional radiofrequency 3 sessions application

Promestriene vaginal use during 3 months

Outcomes

Primary Outcome Measures

Life's quality questionnaire
It was acessed at the beginnig and in the end of the treatment. We used the Short Form Health Survey 36 questionnaire for this parameter. It contains 36 items measuring eight dimensions, that vary the pontuation between 1-5 to 1-6. All but one of the 36 items are used to score the SF-36 eight domains that are aggregated in two summary measures, Physical and Mental components. Among the eight domains, three scales (Physical Functioning, Role-Physical, and Bodily Pain) contributes mostly to the Physical Component Summary (PCS) and three (Mental Health, Role-Emotional, and Social Functioning) contributes to the Mental Component Summary. The domains Vitality, General Health, and Social Functioning present noteworthy correlations with both summary componentNormalized scores below 50 are interpreted as below the generals population. The better is to have a higher pontuation.

Secondary Outcome Measures

Sexuality questionnaire - Female Sexual Function Index
This questionnaire analyses 6 parameters: desire, excitation, lubrication, orgasm, satisfaction and pain. Tha maximum pontuation for each parameter is 6, and for the entire questionnaire is 36 (the best pontuation).
pH values
We used a pH tape to determine the vaginal pH. The normal measure é between 3,8 and 4,5.
score symptoms
Patients describe these symptoms dryness, itching, burnig and pain as absent (0 points); mild :1 point; moderate : 2 points and severe : 3 points, at the begging and in the end of the treatment. The best pontuation is zero and the worst is 12.

Full Information

First Posted
August 28, 2018
Last Updated
January 20, 2021
Sponsor
University of Sao Paulo General Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT04717245
Brief Title
Comparative Study: Vaginal Promestriene Use, Fractional CO2 LASER and Radiofrequency in the Vaginal Atrophy Treatment
Official Title
Comparative Study : The Effect of Vaginal Estrogen Use, Fractional CO2 LASER and Microablative Fractional Radiofrequency in the Treatment of Vaginal Atrophy: Clinical, Histological, Immunohistochemical and Molecular Biology Study
Study Type
Interventional

2. Study Status

Record Verification Date
August 2018
Overall Recruitment Status
Completed
Study Start Date
October 25, 2018 (Actual)
Primary Completion Date
March 7, 2019 (Actual)
Study Completion Date
February 18, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Sao Paulo General Hospital

4. Oversight

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

5. Study Description

Brief Summary
Postmenopausal hypoestrogenism may determine genital atrophy, which may be accompanied by a non-specific inflammatory process and may hinder or even prevent sexual intercourse. In more severe cases, the patient may have local pain that interferes with their daily activities. The best treatment for increasing genital trophism is still estrogen. However, there are women who can not use this therapy or do not want it. Therefore, there is a need for alternatives, such as ablation techniques: use of CO2 LASER and fractional radiofrequency. The study was carried out at the outpatient clinic of Lower Genital Tract ambulatory of the Discipline of Gynecology, Department of Obstetrics and Gynecology, Clinical Hospital, Faculty of Medicine, University of São Paulo, involving 75 women who were divided after randomization in three groups: Group 1 - treatment with topical vaginal promestriene (n = 25 patients); Group 2 - treatment with fractional CO2 LASER (n = 25 patients); Group 3 - fractional microablative radiofrequency treatment (n = 25 patients). An evaluation of the complaints were be performed through questionnaires on sexuality, quality of life and urinary incontinence, as well as biopsies of the vaginal wall for histomorphometric, immunohistochemical and molecular biology study before and after six months of treatment. The duration of the study were fifteen months.
Detailed Description
After completing the eligibility criteria, patients signed the consent inform. Division of groups: Were included in the study 75 patients, divided into three groups: Group 1 - Treatment with topical vaginal promestriene - 25 patients in this group were included patients free of systemic or topical hormonal treatment for at 3 months Group 2 - Treatment with CO2 LASER - 25 patients, in this group were included patients free of systemic or topical hormonal treatment for at 3 months. Group 3 - Treatment with microablative fractionated radiofrequency - 25 patients in this group were included patients free of systemic or topical hormonal treatment for at least 3 months. The present study was open and randomized. The randomization was be performed through the software "Test Generator Software Standard Edition" At the first visit, all patients responded to the clinical questionnaire of female sex quotient (QS-F), the quality of life questionnaire (SF-36) and the urinary incontinence questionnaire. All patients were submitted to specular gynecological examination to collect cervical-vaginal cytology, biopsy of 1/3 proximal vaginal wall for histological analysis and immunohistochemistry. After the results of the examinations and possible treatments required, the patients were referred for the proposed treatments according to their randomized group. Sampling Cytology :Cervical and vaginal oncology cytology were collected through a smear on a slide with fixative. The histological expression of the following immunohistochemical parameters will be evaluated: Presence and density of estrogen receptors Vascular density Thickness of the epithelium Density of collagen fibers Vaginal microbiota Vaginal pH In this study, it will be done a Morphological Analysis, a Histomorphometric analysis and e Immunohistochemical analysis.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Vaginal Atrophy
Keywords
genital atrophy, fractional CO2 laser, microablative fractional radiofrequency, quality of life, sexuality, promestriene, Menopause genitourinary syndrome

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
In this study, 75 patients were included, divided into these three groups: Group 1 - Treatment with topical vaginal promestriene - 25 patients were included in this group Group 2 - Treatment with fractional CO2 LASER - 25 patients were included in this group Group 3 - Treatment with microablative fractional radiofrequency - 25 patients were included in this group
Masking
None (Open Label)
Allocation
Randomized
Enrollment
75 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Fractional CO2 LASER
Arm Type
Active Comparator
Arm Description
Vaginal fractional CO2 LASER 3 sessions applications
Arm Title
Microablative fractional radiofrequency
Arm Type
Active Comparator
Arm Description
Vaginal Microablative fractional radiofrequency 3 sessions application
Arm Title
Promestriene Vaginal
Arm Type
Active Comparator
Arm Description
Promestriene vaginal use during 3 months
Intervention Type
Drug
Intervention Name(s)
Promestriene Vaginal
Other Intervention Name(s)
Promestrieno
Intervention Description
Patients used promestriene vaginal cream for 3 months. The use was recommended to be diary fot the first 2 weeks, and then, repeat every 3 days.
Intervention Type
Other
Intervention Name(s)
Fractional CO2 LASER
Intervention Description
LASER treatment with fractional CO2 Laser was performed in 3 sessions with intervals of 4 weeks between them. Before each session, the patients underwent specular examination. Fractional CO2 LASER was applied following these parameters, fixed in all sessions: vagina wall - power40 W, dwel time 1000 mcs, spacing 1000 mcm and stack 2, vestibule - power 10W, dwel time 500mcs, spacing 300mcg and satck 1
Intervention Type
Other
Intervention Name(s)
Microablative Fractional radiofrequency
Intervention Description
Microablative fractional radiofrequency was performed with the equipment calibrated in FRAXX mode, 45W, Low Energy program 40 milliseconds in the vaginal and introitus wall. Lidocaine spray was applied to vaginal introitus before the procedure. The patient was in the gynecological position. The vaginal speculum was placed and, afterwards, the vaginal antisepsis was performed with aqueous chlorhexidine and cleaning with 0.9% saline solution. All liquid contents were wiped off before beginning the procedure. The fractured tip will be pressed lightly and as perpendicular as possible into the vulvar or vaginal surface, ensuring full contact of all points in the tissue, starting at the lateral vaginal walls and from the proximal to the distal third.
Primary Outcome Measure Information:
Title
Life's quality questionnaire
Description
It was acessed at the beginnig and in the end of the treatment. We used the Short Form Health Survey 36 questionnaire for this parameter. It contains 36 items measuring eight dimensions, that vary the pontuation between 1-5 to 1-6. All but one of the 36 items are used to score the SF-36 eight domains that are aggregated in two summary measures, Physical and Mental components. Among the eight domains, three scales (Physical Functioning, Role-Physical, and Bodily Pain) contributes mostly to the Physical Component Summary (PCS) and three (Mental Health, Role-Emotional, and Social Functioning) contributes to the Mental Component Summary. The domains Vitality, General Health, and Social Functioning present noteworthy correlations with both summary componentNormalized scores below 50 are interpreted as below the generals population. The better is to have a higher pontuation.
Time Frame
3-4 months
Secondary Outcome Measure Information:
Title
Sexuality questionnaire - Female Sexual Function Index
Description
This questionnaire analyses 6 parameters: desire, excitation, lubrication, orgasm, satisfaction and pain. Tha maximum pontuation for each parameter is 6, and for the entire questionnaire is 36 (the best pontuation).
Time Frame
3-4 months
Title
pH values
Description
We used a pH tape to determine the vaginal pH. The normal measure é between 3,8 and 4,5.
Time Frame
3-4 months
Title
score symptoms
Description
Patients describe these symptoms dryness, itching, burnig and pain as absent (0 points); mild :1 point; moderate : 2 points and severe : 3 points, at the begging and in the end of the treatment. The best pontuation is zero and the worst is 12.
Time Frame
3-4 months

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age equal or superior to 40 years and under 65 years Clinical menopause - last menstrual period from 1 to 5 years from the date of recruitment FSH measurement> 25 IU / ml, estrogen <20 æg / ml Patients with vaginal atrophy and clinical and / or sexual symptoms Patients without hormonal treatment for at least five years Exclusion Criteria: Whole Hymen Altered oncology cytology of the cervix and / or vagina Vaginal infections Connective tissue diseases Immunosuppression Coagulation change Diabetes Mellitus Thyroid diseases Use of systemic or local feminine hormones Use of other substances with estrogenic properties
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jose Maria Soares Junior, PHD
Organizational Affiliation
Universidade de São Paulo departamento de ginecologia
Official's Role
Study Director
Facility Information:
Facility Name
Disciplina de ginecologia - departamento de ginecologia e obstetrícia - faculdade de medicina da USP
City
São Paulo
ZIP/Postal Code
01246-100
Country
Brazil

12. IPD Sharing Statement

Plan to Share IPD
No

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Comparative Study: Vaginal Promestriene Use, Fractional CO2 LASER and Radiofrequency in the Vaginal Atrophy Treatment

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