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临床试验/NCT04228679
NCT04228679已完成不适用

The Affect of Erbium Laser Treatments on Vaginal Looseness and Sexual Dysfunction in Pre-menopausal Female Individuals.

Rambam Health Care Campus1 个研究点 分布在 1 个国家目标入组 106 人开始时间: 2020年4月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
106
试验地点
1
主要终点
Female sexual function index.

研究概览

简要总结

Patients with a primary complaint of vaginal looseness and sexual dysfunction, visiting a sexual dysfunction clinic at a tertiary medical center will undergo randomization to either a series of 3 laser treatments or 3 sham treatments, and the effect of these treatments will be measured by several validated questionaires and by means of gynecological examination.

详细描述

Patients suffering from vaginal looseness and sexual dysfunction, as a primary sexual dysfunction complaint will be recruited, sign an informed consent and will receive a thorough explanation regarding the side effects and possible beneficial affects the laser treatments may bestow.

Patients will undergo randomization to either a series of 3 laser treatments or 3 sham treatments, and the effect of these treatments will be measured by several validated questionaires and by means of gynecological examination.

Follow up after treatment cessation will be for 12 months post-treatment.

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
Single (Participant)

入排标准

年龄范围
30 Years 至 55 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Premenopausal women.
  • Women with vaginal looseness and sexual dysfunction as a primary complaint.

排除标准

  • Vaginal bleeding of unknown source.
  • Repeated vaginal infections.
  • Known or suspected cervical pre-malignant neoplasia.
  • Previous treatment with vaginal laser or other forms of energy-based treatment modalities.
  • Pregnancy.
  • Current pelvic inflammatory disease or urinary tract infection.
  • Vaginal surgery during the year preceding study participation.
  • Treatment with systemic or vaginal hormone replacement therapy.
  • Current pelvic floor physiotherapy.

结局指标

主要结局

Female sexual function index.

时间窗: From recruitment up to 15 months.

Female sexual function index scores pre- and post-treatment. Minimal score is 2, maximal score is 36. Thee higher the score, the improved the sexual function is.

次要结局

  • Vaginal health index(From recruitment up to 15 months.)
  • Pelvic floor disability index.(From recruitment up to 15 months.)
  • Monthly sexual intercourse rate(From recruitment up to 15 months.)
  • Vaginal laxity questionnaire.(From recruitment up to 15 months.)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

ROY LAUTERBACH MD

Principal investigator

Rambam Health Care Campus

研究点 (1)

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