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临床试验/NCT03572075
NCT03572075Unknown不适用

Evaluation of the Efficacy of Pelvic Floor Physiotherapy in Symptomatic Patients Affected by Deep Infiltrating Endometriosis

IRCCS Azienda Ospedaliero-Universitaria di Bologna2 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2018年6月15日最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
80
试验地点
2
主要终点
Evaluation of the impact of pelvic floor physiotherapy on urinary function

研究概览

简要总结

The aim of our study is to evaluate the impact of pelvic floor physiotherapy in symptomatic patients affected by deep infiltrating endometriosis, using 3D/4D transperineal ultrasound for evaluation of pelvic floor morphometry, NRS (Numerical Rating Scale) for evaluation of symptoms and validated questionnaires investigating intestinal, sexual and urinary functions.

These results will be compared with those obtained from symptomatic patients affected by deep infiltrating endometriosis following the standard care procedure that does not provide pelvic floor physiotherapy.

详细描述

Symptomatic, nulliparous women with deep infiltrating endometriosis are included in the study.

During the first medical examination, endometriosis related symptoms are assessed using NRS (Numerical Rating Scale); intestinal, sexual and urinary functions are evaluated with validated questionnaires (Knowles-Eccersley-Scott-Symptom Questionnaire (KESS), Female Sexual Function Index (FSFI), Bristol Female Lower Urinary Tract Symptoms (BFLUTS)); pelvic floor morphometry at rest, during pelvic floor contraction and during Valsalva manoeuvre is evaluated using 3D/4D transperineal ultrasound through the assessment of the levator hiatus area (LHA). Gynaecological examination, transvaginal and transabdominal ultrasound are performed.

After the first medical examination, enrolled patients are randomized into two groups: patients in Group A receive standard care procedure and pelvic floor physiotherapy; patients in Group B receive standard care procedure only. Pelvic floor physiotherapy protocol consists of six sessions (weeks 1, 3, 5, 8, 11 from the randomization). After four months from the first medical examination, endometriosis related symptoms, intestinal, sexual and urinary functions and pelvic floor morphometry are reassessed for all patients, using the same procedures, comparing the two groups and evaluating the impact of pelvic floor physiotherapy.

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
None

入排标准

年龄范围
18 Years 至 50 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Patients with clinical and ultrasound diagnosis of deep endometriosis with related symptoms (chronic pelvic pain, dysmenorrhea, dyschezia, dyspareunia, dysuria)
  • Nulliparity
  • Obtaining Informed Consent

排除标准

  • Patients with an oncological disease or needing surgery for malignant pathologies
  • Urogenital prolapse
  • History of surgery for deep infiltrating endometriosis
  • Congenital or acquired malformations of pelvis and pelvic floor
  • History of diseases characterised by chronic pelvic pain (interstitial cystitis, irritable bowel disease, chronic vulvodynia).

研究组 & 干预措施

Group A

Experimental

assessment of symptoms at the first medical examination; standard care protocol; pelvic floor physiotherapy; assessment of symptoms after four months

干预措施: assessment of symptoms at the first medical examination (Diagnostic Test)

Group A

Experimental

assessment of symptoms at the first medical examination; standard care protocol; pelvic floor physiotherapy; assessment of symptoms after four months

干预措施: pelvic floor physiotherapy (Procedure)

Group A

Experimental

assessment of symptoms at the first medical examination; standard care protocol; pelvic floor physiotherapy; assessment of symptoms after four months

干预措施: standard care protocol (Procedure)

Group A

Experimental

assessment of symptoms at the first medical examination; standard care protocol; pelvic floor physiotherapy; assessment of symptoms after four months

干预措施: assessment of symptoms after four months (Diagnostic Test)

Group B

Experimental

assessment of symptoms at the first medical examination; standard care protocol; assessment of symptoms after four months

干预措施: assessment of symptoms after four months (Diagnostic Test)

Group B

Experimental

assessment of symptoms at the first medical examination; standard care protocol; assessment of symptoms after four months

干预措施: assessment of symptoms at the first medical examination (Diagnostic Test)

Group B

Experimental

assessment of symptoms at the first medical examination; standard care protocol; assessment of symptoms after four months

干预措施: standard care protocol (Procedure)

结局指标

主要结局

Evaluation of the impact of pelvic floor physiotherapy on urinary function

时间窗: After four months from the randomization

Evaluation of the impact of pelvic floor physiotherapy on symptomatic patients, using a validated questionnaire (Bristol Female Lower Urinary Tract Symptoms (BFLUTS)).

Evaluation of the impact of pelvic floor physiotherapy on pelvic floor muscles contraction

时间窗: After four months from the randomization

Evaluation of the impact of pelvic floor physiotherapy on pelvic floor muscles contraction and pain using a gynecological examination and ultrasounds. All scans are obtained using a Voluson E6 system (GE Healthcare, Zipf, Austria) with RAB 8-4-MHz volume transducer for all acquisitions. Measurements were evaluated using a dedicated software (4DView 14.4; GE Healthcare, Zipf, Austria).

Evaluation of the impact of pelvic floor physiotherapy on intestinal function

时间窗: After four months from the randomization

Evaluation of the impact of pelvic floor physiotherapy on symptomatic patients, using a validated questionnaire (Knowles-Eccersley-Scott-Symptom Questionnaire (KESS).

Evaluation of the impact of pelvic floor physiotherapy on sexual function

时间窗: After four months from the randomization

Evaluation of the impact of pelvic floor physiotherapy on symptomatic patients, using a validated questionnaire (Female Sexual Function Index (FSFI)).

次要结局

  • Evaluation of the 3D-4D transperineal ultrasound as a bio-feedback tool(After 1, 3, 5, 8, 11 weeks from the randomization)
  • Evaluation of uro-genital hiatus using 3D-4D transperineal ultrasound(At randomization and after four months from the randomization)

研究者

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

Mohamed Mabrouk

Principal investigator

IRCCS Azienda Ospedaliero-Universitaria di Bologna

研究点 (2)

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