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Light Emitting Diode for theTreatment of Genitourinary Syndrome of Menopause Associated With Breast Cancer Treatment (LEDCA)

Primary Purpose

Atrophy;Vaginal, Breast Cancer

Status
Recruiting
Phase
Not Applicable
Locations
Brazil
Study Type
Interventional
Intervention
Experimental: LED group
Sham Comparator: Control
Sponsored by
Centro de Atenção ao Assoalho Pélvico
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Atrophy;Vaginal focused on measuring Vaginal Atrophy, Breast Cancer, Hormonal Therapy, Photodynamic Therapy, Light Emitting Diode

Eligibility Criteria

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

Inclusion Criteria:

  • 18-65 anos
  • Pathological proven Breast Cancer diagnosis
  • Stage 0-III by American Joint Committee on Cancer (AJCC) and International Union Against Cancer (UICC) of Classification of Malignant Tumours, TNM (Acronym for Tumor-Node-Metastasis) 8ª edition
  • Genitourinary Syndrome of Menopause confirmed through patient-reported symptoms and gynecological examination (of external structures, introitus, and vaginal mucosa)
  • Vaginal pH >5,0

Exclusion Criteria:

  • Hormone replacement less than 6 months
  • Diagnosis of vaginal infection
  • Difficulty in understanding the proposed instruments
  • Patients with chronic neurological degenerative diseases that preclude to be on position
  • Metastatic disease
  • Any vaginal photodynamic treatment less than 3 months

Sites / Locations

  • Centro de Atenção ao Assoalho PelvicoRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Sham Comparator

Arm Label

LED group

Control group

Arm Description

Participants who will submitted to active procedure with LED. Both groups will be submitted to kinesiotherapy.

Participants who will submitted to sham procedure with heated gel. Both groups will be submitted to kinesiotherapy.

Outcomes

Primary Outcome Measures

Vaginal maturation index
Cytological vaginal will be collected at 1/3 lower lateral vaginal wall and quantified superficial, intermediate and basal cells to calculate vaginal maturation index
Female Sexual Function Index (FSFI) - Female Version (QS-F)
Measure of quality of sex life. Full Scale Score Range 2-36

Secondary Outcome Measures

Vaginal pH
pH indicator tape
Quality of life by FACT B
Functional Assessment of Chronic Therapy- Breast (FACT B) Questionary validated to Portuguese to measure quality of life in breast cancer patients (Total score and Subscale). Graduated 0-128 (lower values means worse quality of life). Physical Wellbeing (PWB) 0-28; Social/Family Wellbeing (SWB) 0-28; Emotional Wellbeing (EWB) 0-24; Funtional Wellbeing (FWB) 0-28; Breast Cancer Subscale (BCS) 0-40. Total Score do not include Arm Subscale (ARM) 0-20
Urinary symptoms
International Consultation on Incontinence Questionnaire - Short Form (ICIQ Questionary Short Form)-Scoring scale: 0-21 (lower values means better quality of life)
Visual analog scale
Stratification between 0 and 10 (few symptoms to severe symptoms)
Female Genital Self-Image Scale - 7 (FGSIS-7)
Measure of quality of sex life. Scores between 7-28 (higher scores indicate better self-image)
Likert scale
Satisfaction with the treatment measured between 1 and 5 ( not at all happy with the treatment -very happy with the treatment)
Sexual Quotients Female Version (QS-F)
Female sex life domain. Scores between 0-100 (higher scores indicate better sex life) Scores between 82-100 score: excellent, 62-80 score: regular, 42-60 score: unfavorable, 22-40 score: regular, 0-20 score: bad
SF-36
Short Form health survey 36 questionnaire, (0-100) - lower values means worse quality of life

Full Information

First Posted
December 16, 2018
Last Updated
June 21, 2023
Sponsor
Centro de Atenção ao Assoalho Pélvico
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1. Study Identification

Unique Protocol Identification Number
NCT03833726
Brief Title
Light Emitting Diode for theTreatment of Genitourinary Syndrome of Menopause Associated With Breast Cancer Treatment
Acronym
LEDCA
Official Title
Light Emitting Diode for the Treatment of Genitourinary Syndrome of Menopause Associated With Hormonal Therapy for Treating Breast Cancer: Randomized Controlled Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
June 2023
Overall Recruitment Status
Recruiting
Study Start Date
January 30, 2019 (Actual)
Primary Completion Date
August 2023 (Anticipated)
Study Completion Date
September 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Centro de Atenção ao Assoalho Pélvico

4. Oversight

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

5. Study Description

Brief Summary
Breast Cancer treatment may cause several side effects, some long lasting. Adjuvant hormone therapy helps avoiding recurrence triggers vulvovaginal atrophy syndrome. This study evaluate a photodynamic treatment with light emitting diode to improve vaginal dryness and irritation, pruritus, pain or discomfort in intercourse.
Detailed Description
The Genitourinary Menopause Syndrome (MMS) affects up to 70% of in treatment breast cancer patients. Symptoms are due to a decrease in hormone levels or block to circulating hormones and induce functional changes in the vagina cutting in quality of life and impacting sexual function. This is a randomized, double blind trial in a sample of 74 individuals that will be performed at an specialized Pelvic Floor Care Center (CAAP) in Brazil. Will be included women age between 18 and 65 years, in adjuvant hormone therapy, with clinical signs and symptoms of vulvovaginal atrophy syndrome and cytologic evidence of atrophy, (pH <5.0 and vaginal cytology with predominance of superficial cells). Will be excluded from the study the patients in hormonal replacement for less than 6 months, diagnosis of vaginal infection, pregnant women, difficulty understanding the proposed instruments and patients with chronic neurological degenerative diseases. Three 405 nm light emitting diode (LED) sessions will be performed, with a seven days interval between them compared with sham procedure, and both groups will perform five sessions of kinesiotherapy sessions. Maturation vaginal index will be checked before and after all treatment and self- administered questionnaires will be performed before each session with Female Sexual Function Index (FSFI) - Female Version (QS-F), Female Genital Self-Image Scale - 7 (FGSIS-7), International Consultation on Incontinence Questionnaire - Short Form, (ICIQ-SF), Functional Assessment Of Cancer Therapy - Breast Cancer (FACT-B). At the end of treatment, the visual analog scale and Likert scale will be used to measure the individual's satisfaction

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Atrophy;Vaginal, Breast Cancer
Keywords
Vaginal Atrophy, Breast Cancer, Hormonal Therapy, Photodynamic Therapy, Light Emitting Diode

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
The study will be conducted women diagnosed with Genitourinary Syndrome of Menopause treated with kinesiotherapy, divided in two groups: LED treatment or LED Sham.
Masking
ParticipantCare Provider
Masking Description
The participant will be randomly divided between LED group or LED Sham procedure that will consist of turned off device and heated gel and both patients and physiotherapists of kinesiotherapy phase wont be aware with group the participant is allocated.
Allocation
Randomized
Enrollment
74 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
LED group
Arm Type
Experimental
Arm Description
Participants who will submitted to active procedure with LED. Both groups will be submitted to kinesiotherapy.
Arm Title
Control group
Arm Type
Sham Comparator
Arm Description
Participants who will submitted to sham procedure with heated gel. Both groups will be submitted to kinesiotherapy.
Intervention Type
Procedure
Intervention Name(s)
Experimental: LED group
Intervention Description
5 Sessions of 8 minute 405 nm Blue Light Emitting Diode, LED, with a power of 1.66 W / m2, 7 days apart.
Intervention Type
Procedure
Intervention Name(s)
Sham Comparator: Control
Intervention Description
5 Sessions of 8 minute with device off and heated gel, 7 days apart.
Primary Outcome Measure Information:
Title
Vaginal maturation index
Description
Cytological vaginal will be collected at 1/3 lower lateral vaginal wall and quantified superficial, intermediate and basal cells to calculate vaginal maturation index
Time Frame
Change from baseline at 3 months
Title
Female Sexual Function Index (FSFI) - Female Version (QS-F)
Description
Measure of quality of sex life. Full Scale Score Range 2-36
Time Frame
Change from baseline at 3 months
Secondary Outcome Measure Information:
Title
Vaginal pH
Description
pH indicator tape
Time Frame
Change from baseline at 3 months
Title
Quality of life by FACT B
Description
Functional Assessment of Chronic Therapy- Breast (FACT B) Questionary validated to Portuguese to measure quality of life in breast cancer patients (Total score and Subscale). Graduated 0-128 (lower values means worse quality of life). Physical Wellbeing (PWB) 0-28; Social/Family Wellbeing (SWB) 0-28; Emotional Wellbeing (EWB) 0-24; Funtional Wellbeing (FWB) 0-28; Breast Cancer Subscale (BCS) 0-40. Total Score do not include Arm Subscale (ARM) 0-20
Time Frame
Change from baseline at 3 months
Title
Urinary symptoms
Description
International Consultation on Incontinence Questionnaire - Short Form (ICIQ Questionary Short Form)-Scoring scale: 0-21 (lower values means better quality of life)
Time Frame
Change from baseline at 3 months
Title
Visual analog scale
Description
Stratification between 0 and 10 (few symptoms to severe symptoms)
Time Frame
Change from baseline at 3 months
Title
Female Genital Self-Image Scale - 7 (FGSIS-7)
Description
Measure of quality of sex life. Scores between 7-28 (higher scores indicate better self-image)
Time Frame
Change from baseline at 3 months
Title
Likert scale
Description
Satisfaction with the treatment measured between 1 and 5 ( not at all happy with the treatment -very happy with the treatment)
Time Frame
Change from finished treatment and 3 months after
Title
Sexual Quotients Female Version (QS-F)
Description
Female sex life domain. Scores between 0-100 (higher scores indicate better sex life) Scores between 82-100 score: excellent, 62-80 score: regular, 42-60 score: unfavorable, 22-40 score: regular, 0-20 score: bad
Time Frame
Change from baseline at 3 months
Title
SF-36
Description
Short Form health survey 36 questionnaire, (0-100) - lower values means worse quality of life
Time Frame
Change from baseline at 3 months

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 18-65 anos Pathological proven Breast Cancer diagnosis Stage 0-III by American Joint Committee on Cancer (AJCC) and International Union Against Cancer (UICC) of Classification of Malignant Tumours, TNM (Acronym for Tumor-Node-Metastasis) 8ª edition Genitourinary Syndrome of Menopause confirmed through patient-reported symptoms and gynecological examination (of external structures, introitus, and vaginal mucosa) Vaginal pH >5,0 Exclusion Criteria: Hormone replacement less than 6 months Diagnosis of vaginal infection Difficulty in understanding the proposed instruments Patients with chronic neurological degenerative diseases that preclude to be on position Metastatic disease Any vaginal photodynamic treatment less than 3 months
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Patrícia V Lordêlo, PhD
Phone
+5571988592400
Email
pvslordelo@hotmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Daniela B de Oliveira, MD
Phone
+55 71 988469597
Email
danielagbarros@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Patríca V Lordelo, PhD
Organizational Affiliation
Centro de Atenção Pélvica- CAAP
Official's Role
Study Chair
Facility Information:
Facility Name
Centro de Atenção ao Assoalho Pelvico
City
Salvador
State/Province
Ba
ZIP/Postal Code
40.290-000
Country
Brazil
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Patricia V Lordelo, Phd
Phone
+5571988592400
Email
pvslordelo@hotmail.com

12. IPD Sharing Statement

Citations:
PubMed Identifier
25815692
Citation
Lester J, Pahouja G, Andersen B, Lustberg M. Atrophic vaginitis in breast cancer survivors: a difficult survivorship issue. J Pers Med. 2015 Mar 25;5(2):50-66. doi: 10.3390/jpm5020050.
Results Reference
background
PubMed Identifier
23805799
Citation
Kyvernitakis I, Ziller V, Hars O, Bauer M, Kalder M, Hadji P. Prevalence of menopausal symptoms and their influence on adherence in women with breast cancer. Climacteric. 2014 Jun;17(3):252-9. doi: 10.3109/13697137.2013.819327. Epub 2013 Aug 25.
Results Reference
background
PubMed Identifier
25179577
Citation
Portman DJ, Gass ML; Vulvovaginal Atrophy Terminology Consensus Conference Panel. Genitourinary syndrome of menopause: new terminology for vulvovaginal atrophy from the International Society for the Study of Women's Sexual Health and the North American Menopause Society. Maturitas. 2014 Nov;79(3):349-54. doi: 10.1016/j.maturitas.2014.07.013. Epub 2014 Aug 19.
Results Reference
background
PubMed Identifier
7731384
Citation
Nilsson K, Risberg B, Heimer G. The vaginal epithelium in the postmenopause--cytology, histology and pH as methods of assessment. Maturitas. 1995 Jan;21(1):51-6. doi: 10.1016/0378-5122(94)00863-3.
Results Reference
background
PubMed Identifier
30289755
Citation
Moreno AC, Sikka SK, Thacker HL. Genitourinary syndrome of menopause in breast cancer survivors:Treatments are available. Cleve Clin J Med. 2018 Oct;85(10):760-766. doi: 10.3949/ccjm.85a.17108. Erratum In: Cleve Clin J Med. 2018 Nov;85(11):860.
Results Reference
background
PubMed Identifier
28154914
Citation
Arunkalaivanan A, Kaur H, Onuma O. Laser therapy as a treatment modality for genitourinary syndrome of menopause: a critical appraisal of evidence. Int Urogynecol J. 2017 May;28(5):681-685. doi: 10.1007/s00192-017-3282-y. Epub 2017 Feb 2.
Results Reference
background
PubMed Identifier
26617271
Citation
Yaralizadeh M, Abedi P, Najar S, Namjoyan F, Saki A. Effect of Foeniculum vulgare (fennel) vaginal cream on vaginal atrophy in postmenopausal women: A double-blind randomized placebo-controlled trial. Maturitas. 2016 Feb;84:75-80. doi: 10.1016/j.maturitas.2015.11.005. Epub 2015 Nov 12.
Results Reference
background
Links:
URL
http://evs.nci.nih.gov/ftp1/CTCAE
Description
NCI Toxicity Scale

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Light Emitting Diode for theTreatment of Genitourinary Syndrome of Menopause Associated With Breast Cancer Treatment

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