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Evaluation of Fractional CO2 Laser Treatment Efficacy and Comparison to Vaginal Estrogen Therapy in Postmenopausal Women With Vulvovaginal Atrophy

Primary Purpose

Vulvovaginal Atrophy

Status
Completed
Phase
Phase 3
Locations
Brazil
Study Type
Interventional
Intervention
CO2 laser
Estrogen
Placebo of Estrogen
Placebo of CO2 laser
Sponsored by
Faculdade de Medicina do ABC
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Vulvovaginal Atrophy focused on measuring Vulvovaginal atrophy, Menopause, Fractional CO2 laser, Estrogen cream

Eligibility Criteria

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

Inclusion Criteria:

  • 45-65 women with amenorrhea for over 24 months.
  • Clinical vaginal atrophy diagnosis.

Exclusion Criteria:

  • BMI > 35.
  • Previous use of oral estrogen therapy in the last 6 months.
  • History or current diagnosis of cancer.
  • Altered cervical smear in the last 12 months.
  • Renal or hepatic insufficiency.
  • Drug-induced menopause.
  • Previous use of steroids.
  • Previous vaginal radiotherapy therapy.
  • Vulvovaginitis.

Sites / Locations

  • Centro de Atencao a Saude da Mulher

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Active Comparator

Sham Comparator

Arm Label

CO2 laser & Estrogen

CO2 laser & Placebo of Estrogen

Placebo of CO2 laser & Estrogen

Arm Description

Effective fractional CO2 laser therapy and effective estrogen vaginal cream

Effective fractional CO2 laser therapy and placebo of estrogen vaginal cream.

Placebo fractional CO2 laser therapy and effective estrogen vaginal cream.

Outcomes

Primary Outcome Measures

Change from Baseline in Vulvovaginal Symptom Questionnaire
Vulvovaginal Symptom Questionnaire will be used to evaluate improvement of vulvovaginal atrophy symptoms.

Secondary Outcome Measures

Vaginal Cytology Improvement
Vaginal cytology will be obtained from the middle third lateral vaginal wall in order to evaluate initial conditions of the vaginal wall and modifications after treatment. Frost Index, Karyopyknotic Index and Eosinophilic Index will be applied to each sample to measure improvement of vaginal atrophy.
Change from Baseline in Female Sex Function Index
Female Sex Function Index will be used to evaluate improvement of vulvovaginal atrophy symptoms.
Change from Baseline in The Menopause-Specific Quality of Life
The Menopause-Specific Quality of Life will be used to evaluate improvement of vulvovaginal atrophy symptoms.

Full Information

First Posted
April 6, 2015
Last Updated
June 24, 2016
Sponsor
Faculdade de Medicina do ABC
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1. Study Identification

Unique Protocol Identification Number
NCT02419729
Brief Title
Evaluation of Fractional CO2 Laser Treatment Efficacy and Comparison to Vaginal Estrogen Therapy in Postmenopausal Women With Vulvovaginal Atrophy
Official Title
Evaluation of Fractional CO2 Laser Treatment Efficacy and Comparison to Vaginal Estrogen Therapy in Postmenopausal Women With Vulvovaginal Atrophy
Study Type
Interventional

2. Study Status

Record Verification Date
June 2016
Overall Recruitment Status
Completed
Study Start Date
March 2015 (undefined)
Primary Completion Date
October 2015 (Actual)
Study Completion Date
November 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Faculdade de Medicina do ABC

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Forty-five women will be included in a double-blind randomized trial in order to compare fractional CO2 laser treatment, local estrogen therapy and the combination of both treatments for Vulvovaginal Atrophy (VVA) and determine the efficacy and possible adverse effects CO2 laser treatment.
Detailed Description
Vulvovaginal atrophy (VVA) symptoms are strongly associated with declining ovarian function and estrogen levels in postmenopausal women, having a considerable impact on women's life quality. Topical hormonal therapy and hormonal replacement are widely used to alleviate VVA symptoms. In this context, minimal invasive fractional CO2 laser emerges as an alternative non-hormonal therapy, especially in patients that present contraindications to hormonal therapy. Objective: Compare fractional CO2 laser treatment, local estrogen therapy and the combination of both treatments for VVA and determine the efficacy and possible adverse effects CO2 laser treatment. Materials and Methods: Forty-five postmenopausal women will be randomized in three double-blinded groups of treatment consisting of CO2 laser and placebo of estrogen vaginal cream, placebo of CO2 laser and estrogen vaginal cream and CO2 laser and estrogen vaginal cream. Assessment of baseline characteristics and follow-up will be obtained through self-completion questionnaires (Female Sex Function Index, International Consultation on Incontinence Questionnaire-Short Form (ICIQ-SF), Vulvovaginal Symptom Questionnaire and The Menopause-Specific Quality of Life (MENQOL)). Frost Index and Vaginal Health Index (VHI) are part of objective clinical and histologic analyses. Colposcopy, vaginal cytology and middle third lateral vaginal wall biopsy will also be performed at baseline and at week 17.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Vulvovaginal Atrophy
Keywords
Vulvovaginal atrophy, Menopause, Fractional CO2 laser, Estrogen cream

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
45 (Actual)

8. Arms, Groups, and Interventions

Arm Title
CO2 laser & Estrogen
Arm Type
Experimental
Arm Description
Effective fractional CO2 laser therapy and effective estrogen vaginal cream
Arm Title
CO2 laser & Placebo of Estrogen
Arm Type
Active Comparator
Arm Description
Effective fractional CO2 laser therapy and placebo of estrogen vaginal cream.
Arm Title
Placebo of CO2 laser & Estrogen
Arm Type
Sham Comparator
Arm Description
Placebo fractional CO2 laser therapy and effective estrogen vaginal cream.
Intervention Type
Device
Intervention Name(s)
CO2 laser
Other Intervention Name(s)
Fractionated CO2 laser
Intervention Description
SMARTXIDE2 V2LR (DEKA-Pulse) was used in each application using minimal parameters suggested by the laser's software ( Power of 30 W, 1000us emission time, 1000um spacing and a level of SmartStack 2)
Intervention Type
Drug
Intervention Name(s)
Estrogen
Other Intervention Name(s)
Estriol 1mg
Intervention Description
Topical estrogen cream treatment: Estriol 1mg daily.
Intervention Type
Drug
Intervention Name(s)
Placebo of Estrogen
Intervention Description
Placebo of topical estrogen cream.
Intervention Type
Device
Intervention Name(s)
Placebo of CO2 laser
Other Intervention Name(s)
SMARTXIDE2 V2LR - Monalisa Touch - Deka Laser
Intervention Description
SMARTXIDE2 V2LR (DEKA-Pulse) was used in each applications using minimal parameters suggested by the laser's software but power of 0.5 W was stipulated for the placebo intervention and other parameters remained unchanged.
Primary Outcome Measure Information:
Title
Change from Baseline in Vulvovaginal Symptom Questionnaire
Description
Vulvovaginal Symptom Questionnaire will be used to evaluate improvement of vulvovaginal atrophy symptoms.
Time Frame
Baseline, week 10 and week 17
Secondary Outcome Measure Information:
Title
Vaginal Cytology Improvement
Description
Vaginal cytology will be obtained from the middle third lateral vaginal wall in order to evaluate initial conditions of the vaginal wall and modifications after treatment. Frost Index, Karyopyknotic Index and Eosinophilic Index will be applied to each sample to measure improvement of vaginal atrophy.
Time Frame
Baseline, week 10 and week 17
Title
Change from Baseline in Female Sex Function Index
Description
Female Sex Function Index will be used to evaluate improvement of vulvovaginal atrophy symptoms.
Time Frame
Baseline, week 10 and week 17
Title
Change from Baseline in The Menopause-Specific Quality of Life
Description
The Menopause-Specific Quality of Life will be used to evaluate improvement of vulvovaginal atrophy symptoms.
Time Frame
Baseline, week 10 and week 17
Other Pre-specified Outcome Measures:
Title
Urinary Incontinence Improvement
Description
Incontinence Questionnaire-Short Form (ICIQ-SF) will be used in order to evaluate urinary incontinence improvement after treatment.
Time Frame
Baseline, week 10 and week 17
Title
Vaginal Health Index Improvement
Description
Evaluation of vaginal wall conditions such as pH, elasticity, bleeding signs, secretion type and consistency and hydration.
Time Frame
Baseline, week 10 and week 17

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
45 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 45-65 women with amenorrhea for over 24 months. Clinical vaginal atrophy diagnosis. Exclusion Criteria: BMI > 35. Previous use of oral estrogen therapy in the last 6 months. History or current diagnosis of cancer. Altered cervical smear in the last 12 months. Renal or hepatic insufficiency. Drug-induced menopause. Previous use of steroids. Previous vaginal radiotherapy therapy. Vulvovaginitis.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Vera L da Cruz, MD
Organizational Affiliation
Faculdade de Medicina do ABC
Official's Role
Principal Investigator
Facility Information:
Facility Name
Centro de Atencao a Saude da Mulher
City
Sao Bernardo
State/Province
Sao Paulo
ZIP/Postal Code
09770-210
Country
Brazil

12. IPD Sharing Statement

Citations:
PubMed Identifier
25333211
Citation
Salvatore S, Nappi RE, Parma M, Chionna R, Lagona F, Zerbinati N, Ferrero S, Origoni M, Candiani M, Leone Roberti Maggiore U. Sexual function after fractional microablative CO(2) laser in women with vulvovaginal atrophy. Climacteric. 2015 Apr;18(2):219-25. doi: 10.3109/13697137.2014.975197. Epub 2014 Dec 16.
Results Reference
result
PubMed Identifier
15779109
Citation
Society of Obstetricians and Gynaecologists of Canada. SOGC clinical practice guidelines. The detection and management of vaginal atrophy. Number 145, May 2004. Int J Gynaecol Obstet. 2005 Feb;88(2):222-8. doi: 10.1016/j.ijgo.2004.11.003.
Results Reference
result
Citation
Bachman GA. A new option for managing urogenital atrophy in post-menopausal women. Cont Obstet Gynecol 42, pp. 13-28.
Results Reference
result
PubMed Identifier
24605832
Citation
Salvatore S, Nappi RE, Zerbinati N, Calligaro A, Ferrero S, Origoni M, Candiani M, Leone Roberti Maggiore U. A 12-week treatment with fractional CO2 laser for vulvovaginal atrophy: a pilot study. Climacteric. 2014 Aug;17(4):363-9. doi: 10.3109/13697137.2014.899347. Epub 2014 Jun 5.
Results Reference
result

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Evaluation of Fractional CO2 Laser Treatment Efficacy and Comparison to Vaginal Estrogen Therapy in Postmenopausal Women With Vulvovaginal Atrophy

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