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临床试验/NCT03833726
NCT03833726已完成不适用

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

Centro de Atenção ao Assoalho Pélvico1 个研究点 分布在 1 个国家目标入组 77 人开始时间: 2019年1月30日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
77
试验地点
1
主要终点
Female Sexual Function Index (FSFI) - Female Version (QS-F)

研究概览

简要总结

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.

详细描述

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).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Care Provider)

盲法说明

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.

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • 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

排除标准

  • 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

结局指标

主要结局

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

时间窗: Change from baseline at 3 months

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

Vaginal maturation index

时间窗: 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

次要结局

  • Vaginal pH(Change from baseline at 3 months)
  • Female Genital Self-Image Scale - 7 (FGSIS-7)(Change from baseline at 3 months)
  • Visual analog scale(Change from baseline at 3 months)
  • Quality of life by FACT B(Change from baseline at 3 months)
  • Urinary symptoms(Change from baseline at 3 months)
  • SF-36(Change from baseline at 3 months)
  • Likert scale(Change from finished treatment and 3 months after)
  • Sexual Quotients Female Version (QS-F)(Change from baseline at 3 months)

研究者

发起方
Centro de Atenção ao Assoalho Pélvico
申办方类型
Other
责任方
Sponsor

研究点 (1)

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