Study of the Prevalence of Sexual Dysfunction in Women After Rectal Cancer Surgery and Analysis of the Impact of a Sexologist Intervention

ConditionsRectal Tumor Women Sexuality Life Quality

Trial statusRecruiting

Trial phaseNot applicable

Trial typeInterventional

Biological sexFemale

Age18+

SponsorUniversity Hospital, Limoges

About this trial

RectSexQoL is a study aiming at determining the prevalence of female sexual dysfunction after rectal cancer surgery. It has the goal as well to analyse the impact of an intervention given by a sexologist to such patients.

Eligibility criteria

Qualifiers

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

Disqualifiers

Current pregnancy

Significant cognitive/psychiatric disorders

Guardianship

Trial design

Treatments tested in this trial

sexologist consult
standart of care

Treatment groups

144 Participants

are divided into 2 treatment groups

Sponsors and collaborators

University Hospital, Limoges

Lead sponsor

Source ClinicalTrials.gov