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Clinical Trial Summary

Female patients with either uterine/cervical malignancies will be evaluated for vaginal elasticity using vaginal tactile imaging both before and after radiation treatment.


Clinical Trial Description

Patients will be recruited and sign a consent form. The patients included are patients with either uterine/cervical malignancies. Each participant undergoes radiation treatment either as primary or complementary treatment.

Assessment of vaginal elasticity via vaginal tactile imaging will be performed at 3 different points:

- Before the first treatment session (baseline).

- After the last session of laser treatment.

- 3 months post final treatment. Every patient will serve as her own control. Demographic, gynecologic and obstetric history will be obtained from patients' electronic files. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03667859
Study type Observational
Source Rambam Health Care Campus
Contact
Status Completed
Phase
Start date November 1, 2018
Completion date August 31, 2020

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