RecruitingNCT06132321

Quality of Life in Patients Undergone Vulvar Reconstruction After Vulvar Cancer Resection (3233)

Monocentric Prospective Observational Multiparametric Study on the Quality of Life in Patients Undergone Surgery for Vulvar Cancer and Reconstruction (3233)


Sponsor

Fondazione Policlinico Universitario Agostino Gemelli IRCCS

Enrollment

93 participants

Start Date

Jun 23, 2020

Study Type

OBSERVATIONAL

Conditions

Summary

This study aims to evaluate the patients'quality of life before and after surgery for vulvar cancer and reconstruction, employing different questionnaires and investigating different items.


Eligibility

Sex: FEMALE

Plain Language Summary

Simplified for easier understanding

This observational study examines quality of life outcomes in patients who undergo surgery for vulvar cancer and need reconstructive procedures to restore the area afterward. Researchers want to understand how reconstruction affects patients' wellbeing, body image, and daily functioning. **You may be eligible if...** - You are undergoing surgery for vulvar cancer - You are willing and able to provide informed consent **You may NOT be eligible if...** - You have significant cognitive impairment - You have a psychiatric disorder - You have a neurodegenerative disease (such as dementia or Parkinson's) Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

BEHAVIORALQuality of life questionnaires

Detecting by mean of questionnaires quality of life, urinary function, pain, sexual function and lymphedema status before and after surgery for vulvar cancer, associated or not to vulvar reconstruction


Locations(1)

Fondazione Policlinico Universitario Agostino Gemelli IRCCS

Rome, Italy

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NCT06132321


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