Stricture and atresia of vagina
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Women with a confirmed diagnosis of cervical cancer; patients with an indication for oncological treatment (surgery, radiotherapy, chemotherapy, or brachytherapy); age 18 years or older; ability to understand and sign the Informed Consent Form (ICF)
Exclusion criteria
Exclusion criteria: Patients with metastatic tumors with exclusive indication for palliative treatment; women unable to undergo functional clinical examination (digital palpation); presence of cognitive conditions that prevent the understanding of questionnaires; refusal to participate in any stage of data collection
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To evaluate pelvic floor muscle function, verified by digital palpation, by observing a reduction in strength and endurance levels comparing baseline with post-treatment moments (3 and 6 months) (Oxford Modified Scale);To evaluate female sexual function, verified by the (FSFI - Female Sexual Function Index) questionnaire, by observing variations in total and specific domain scores during follow-up assessments | — |
Secondary
| Measure | Time frame |
|---|---|
| To evaluate the presence and grade of vaginal stenosis, verified by the LENT-SOMA scale, based on the observation of changes in vaginal depth and diameter graded from 1 to 4 according to the severity of sequelae observed at 3 and 6 months post-treatment | — |
Countries
BR
Contacts
Faculdade de Medicina de Ribeirão Preto da Universidade de São Paulo FMRP/USP