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Clinical Trials/NCT03090217
NCT03090217
Unknown
N/A

Pelvic Physiotherapy in the Prevention of Vaginal Stenosis Secondary to Radiotherapy of Gynecological Cancer: a Randomized Controlled Trial

Federal University of Health Science of Porto Alegre1 site in 1 country160 target enrollmentAugust 21, 2017

Overview

Phase
N/A
Intervention
Not specified
Conditions
Gynecologic Cancer
Sponsor
Federal University of Health Science of Porto Alegre
Enrollment
160
Locations
1
Primary Endpoint
Vaginal Stenosis
Last Updated
8 years ago

Overview

Brief Summary

Vaginal stenosis is one of the most prevalent side effects of pelvic radiation, affecting about one third of women. In this randomized controlled trial, the effect of a pelvic physiotherapy protocol on an incidence rate of vaginal stenosis in women with gynecological cancer undergoing gynecological brachytherapy. In addition, the investigators will explore an improvement in quality of life, sexuality, and contractile function of the pelvic floor muscles.

Detailed Description

Tis study will be conducing in a reference hospital to oncology treatment were mane patients with gynecologic cancer are management on radiotherapy services. The aim of this work is evaluated the effects of the pelvic physiotherapy (PP) on the more prevalent constriction pathology (vaginal stenosis) secondary to the brachytherapy. The PP will be conduced by three months after the radiotherapy starts and the incidence of the vaginal stenosis will be compared with a control group throughout six months of fallow-up.

Registry
clinicaltrials.gov
Start Date
August 21, 2017
End Date
July 31, 2018
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Sponsor
Federal University of Health Science of Porto Alegre
Responsible Party
Principal Investigator
Principal Investigator

Fabrício Edler Macagnan

Doctor

Federal University of Health Science of Porto Alegre

Eligibility Criteria

Inclusion Criteria

  • Women over 18 years old;
  • No vaginal stenosis at first evaluation;
  • Women free of previous intracavitary radiation;
  • Women diagnosed with gynecological cancer who are undergoing brachytherapy treatment during the period of research at the Santa Rita Hospital of the Santa Casa de Misericórdia in Porto Alegre;
  • Women who agree to participate in the research through the Informed Consent Form (TCLE).

Exclusion Criteria

  • Women who do not sign the ICF;
  • Women not being treated for gynecological cancer;
  • Women who have a 30% lack of physical therapy sessions (4 sessions);
  • Women who present complications that prevent the accomplishment of the protocol of pelvic physiotherapy or that do not perform all the treatment with brachytherapy.

Outcomes

Primary Outcomes

Vaginal Stenosis

Time Frame: With completion of the study, predicted 15 months after the start of the study.

Vaginal stenosis will be evaluated before the first brachytherapy and twelve months after. Considered according to the study of Kirchheiner et al., (2016) that used the Common Terminology Criteria for Adverse Events (CTCAE v3.0). Vaginal stenosis will also be considered as the narrowing of the vaginal canal that makes it impossible to introduce the number 1 acrylic gynecological speculum through the vaginal introitus.

Secondary Outcomes

  • Sexuality(With completion of the study, predicted 15 months after the start of the study.)
  • Quality of life(With completion of the study, predicted 15 months after the start of the study.)
  • Muscle activity and contractile function of the pelvic floor(With completion of the study, predicted 15 months after the start of the study.)

Study Sites (1)

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