Vaginal Elasticity Assessment Before and After Brachytherapy/Pelvic Radiation
NCT ID: NCT03667859
Last Updated: 2020-09-16
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
25 participants
OBSERVATIONAL
2018-11-01
2020-08-31
Brief Summary
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Detailed Description
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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.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Women undergoing Brachytherapy
Women with either uterine or cervical malignancy treated primarily by brachytherapy.
Vaginal Tactile Imaging
Vaginal elasticity measurements using the Vaginal Tactile Imaging system.
Women undergoing Pelvic Radiation
Women with either uterine or cervical malignancy treated primarily by pelvic radiation.
Vaginal Tactile Imaging
Vaginal elasticity measurements using the Vaginal Tactile Imaging system.
Interventions
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Vaginal Tactile Imaging
Vaginal elasticity measurements using the Vaginal Tactile Imaging system.
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* Women with massive vaginal bleeding.
* Women after pelvic exenteration.
18 Years
75 Years
FEMALE
No
Sponsors
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Rambam Health Care Campus
OTHER
Responsible Party
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ROY LAUTERBACH MD
Principal Investigator
Principal Investigators
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Roy Lauterbach, MD
Role: PRINCIPAL_INVESTIGATOR
Rambam Health Care Campus
Locations
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Rambam health care campus
Haifa, , Israel
Countries
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Other Identifiers
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0398-18-RMB
Identifier Type: -
Identifier Source: org_study_id
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