HPV-Positive pelvic cancer: study probes hidden toll on sex life
NCT ID NCT07523152
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study follows 42 women with HPV-positive pelvic cancer (cervix, vagina, vulva, or anus) to understand how radiotherapy, with or without surgery, affects their sexual quality of life. Participants complete questionnaires about sexual function and emotional distress over time. The goal is to better describe these effects and guide future support strategies.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 42 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Apr 2026
An estimate. Start dates often move.
- Expected to finish
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Oct 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Female participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Women aged 18 or over. 2. Sexually active patients, i.e. those who have been sexually active in the year prior to their cancer diagnosis. 3. Patients being treated at the Montpellier Cancer Institute (ICM). 4. Patient with pelvic squamous cell carcinoma (cervix, vagina, vulva or anus) and human papillomavirus (HPV+) infection 5. Patient aware of her HPV status and how it is transmitted. 6. Indicated for external radiotherapy 7. Patient who has not received any oncological treatment prior to inclusion. 8. Patient who has given verbal consent. Exclusion Criteria: 1. Patients receiving radiotherapy treatment outside the Montpellier Cancer Institute (ICM). 2. Patients who are unwilling or unable to complete the study questionnaires. 3. Patients under guardianship, curatorship or court protection, 4. Patients for whom regular follow-up is impossible for psychological reasons, 5. Patients who do not speak French.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
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