Examining sexual dysfunction in women after rectal cancer surgery and the effects of sexologist intervention
Official title: Study of the Prevalence of Sexual Dysfunction in Women After Rectal Cancer Surgery and Analysis of the Impact of a Sexologist Intervention
Run by University Hospital, Limoges · NCT05933122 · Data updated 2026-11-12
This study looks at how many women have sexual problems after rectal cancer surgery and whether talking to a sex expert can help them feel better compared to standard care.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | Women only |
| Enrollment | 144 (estimated) |
| Sponsor | University Hospital, Limoges Academic / other |
| Drugs / interventions | chemotherapy |
| Locations | 6 sites (Brive-la-Gaillarde and 5 other locations) |
| Status | Recruiting |
| Started | April 3, 2024 |
| Main results expected | May 2027 |
| Study ends | October 2027 |
| Registry record updated | December 2, 2024 |
| Trial ID | NCT05933122 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are women over 18 diagnosed with stage I-III rectal adenocarcinoma who have undergone surgical management.
✕Probably not a fit
Patients who are currently pregnant or have significant cognitive or psychiatric disorders may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study aims to determine how common sexual dysfunction is among women who have undergone surgery for rectal cancer. It will assess the prevalence of these issues before treatment and analyze the impact of consultations with a sexologist on improving sexual well-being. The study will compare outcomes between women receiving sexology consultations and those receiving standard care. By focusing on female patients, it seeks to fill a gap in existing research that has primarily addressed male sexual dysfunction post-cancer treatment.
Why it matters
Potential benefit: If successful, this study could lead to improved sexual health and quality of life for women recovering from rectal cancer surgery.
How similar studies have gone: While there is limited research specifically addressing female sexual dysfunction post-rectal cancer surgery, studies on male patients have shown varying success, indicating a need for more focused investigations like this one.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Women * Diagnosis of stage I-III rectal adenocarcinoma or rectosigmoid junction with anastomosis less than 15 cm from the anal margin * Surgical management, preceded or not by Radio-chemotherapy, with restoration of continuity * Age : over 18 * Proficiency in French or English Exclusion Criteria: * Current pregnancy * Significant cognitive/psychiatric disorders * Guardianship
Where it's running
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Brive Hospital
Brive-la-Gaillarde, France Recruiting -
Les cedres Clinical
Brive-la-Gaillarde, France Recruiting -
Gueret Hospital
Guéret, France Recruiting -
Limoges University Hospital
Limoges, France Recruiting -
Saint Junien Hospital
Saint-Junien, France Recruiting -
Chenieux clinical
Limoges, France Not yet recruiting
Study contacts
- Study coordinator: Niki Christou, MD
- Email: christou.niki19@gmail.com
- Phone: +335 55 05 67 30
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.