Clinical trial Recruiting at 5 sites Interventional Ages 18 and up Women only

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 typeInterventional
Ages18 Years and up
SexWomen only
Enrollment144 (estimated)
SponsorUniversity Hospital, Limoges
Academic / other
Drugs / interventionschemotherapy
Locations6 sites (Brive-la-Gaillarde and 5 other locations)
StatusRecruiting
StartedApril 3, 2024
Main results expectedMay 2027
Study endsOctober 2027
Registry record updatedDecember 2, 2024
Trial IDNCT05933122 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

  • 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

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.