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Completed

NCT Number: NCT03833726

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

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.

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Key information

Age range

18 year–65 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Centro de Atenção ao Assoalho Pelvico

Salvador, Estado de Bahia, 40.290-000, Brazil

About this study

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

Who can participate

Healthy volunteers accepted: No

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

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

Treatment and study plan

Experimental: LED group

Procedure

5 Sessions of 8 minute 405 nm Blue Light Emitting Diode, LED, with a power of 1.66 W / m2, 7 days apart.

Sham Comparator: Control

Procedure

5 Sessions of 8 minute with device off and heated gel, 7 days apart.

Primary outcomes

  1. Vaginal maturation index

    Time frame: Change from baseline at 3 months

    Cytological vaginal will be collected at 1/3 lower lateral vaginal wall and quantified superficial, intermediate and basal cells to calculate vaginal maturation index

  2. Female Sexual Function Index (FSFI) - Female Version (QS-F)

    Time frame: Change from baseline at 3 months

    Measure of quality of sex life. Full Scale Score Range 2-36

Secondary outcomes

  1. Vaginal pH

    Time frame: Change from baseline at 3 months

    pH indicator tape

  2. Quality of life by FACT B

    Time frame: Change from baseline at 3 months

    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

  3. Urinary symptoms

    Time frame: Change from baseline at 3 months

    International Consultation on Incontinence Questionnaire - Short Form (ICIQ Questionary Short Form)-Scoring scale: 0-21 (lower values means better quality of life)

  4. Visual analog scale

    Time frame: Change from baseline at 3 months

    Stratification between 0 and 10 (few symptoms to severe symptoms)

  5. Female Genital Self-Image Scale - 7 (FGSIS-7)

    Time frame: Change from baseline at 3 months

    Measure of quality of sex life. Scores between 7-28 (higher scores indicate better self-image)

  6. Likert scale

    Time frame: Change from finished treatment and 3 months after

    Satisfaction with the treatment measured between 1 and 5 ( not at all happy with the treatment -very happy with the treatment)

  7. Sexual Quotients Female Version (QS-F)

    Time frame: Change from baseline at 3 months

    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

  8. SF-36

    Time frame: Change from baseline at 3 months

    Short Form health survey 36 questionnaire, (0-100) - lower values means worse quality of life

Sponsors and collaborators

Lead sponsor

Centro de Atenção ao Assoalho Pélvico

Other

Registry information

Official study title

Light Emitting Diode for the Treatment of Genitourinary Syndrome of Menopause Associated With Hormonal Therapy for Treating Breast Cancer: Randomized Controlled Clinical Trial

Acronym: LEDCA

Important dates

Study start
2019
Primary completion
2023
Study completion
2023
First posted
Feb 7, 2019
Registry last updated
Dec 5, 2023

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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