Actively Recruiting

Age: 18Years +
All Genders
NCT06517355

Acceptability and Benefits of an Onco-sexology Program for Laryngectomy Patients and Their Partners

Led by Institut Claudius Regaud · Updated on 2025-05-23

45

Participants Needed

1

Research Sites

187 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Single-centre prospective pilot study designed to demonstrate the acceptability of onco-sexology management for laryngectomy patients and their partners in order to improve their perception of their intimate life. This is a non-interventional study (category 3 Loi Jardé), which will not result in any change in patient management. All procedures will be carried out in accordance with standard practice. Patients will be followed for 14 months.

CONDITIONS

Official Title

Acceptability and Benefits of an Onco-sexology Program for Laryngectomy Patients and Their Partners

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patient treated for ORL cancer by total (pharyngo)laryngectomy
  • Patient with WHO performance status 0, 1, or 2
  • Age 18 years or older
  • Patient has not objected to participation in the study
  • Partner (if applicable) aged 18 years or older
  • Partner (if applicable) has not objected to participation in the study
Not Eligible

You will not qualify if you...

  • Patient with another active malignant disease at the time of inclusion
  • Psychological, familial, geographical, or sociological conditions preventing compliance with study follow-up or procedures
  • Patients deprived of liberty or under legal protection (guardianship, tutorship, safeguard of justice)
  • Partners (if applicable) deprived of liberty or under legal protection (guardianship, tutorship, safeguard of justice)

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

IUCT-O

Toulouse, France

Actively Recruiting

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Research Team

J

Julienne VIDAL

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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