Under construction – not a live service
Sign in

2025-521460-36-00RecruitingPhase 4

Prospective randomized study on sexual health and self-perceived quality of life (PROMs) in patients treated for cervical cancer

Source: EU CTIS (euclinicaltrials.eu) · Last updated 20 Aug 2026

Next steps

Brief summary (registry, in English)

To assess the improvement in sexual function and self-perceived quality of life using PROMs (Patient-Reported Outcomes) in patients treated for cervical cancer who undergo a multimodal intervention in the sexual sphere and lifestyle compared to those who undergo care within routine clinical practice.

Status (registry)
Recruiting
Phase (registry)
Phase 4
Study type
Interventional
Enrollment
120 (estimated)
First submitted
14 Mar 2025
Start date
8 May 2026
Lead sponsor
Fundacio De Recerca Clinic Barcelona-Institut D’Investigacions Biomediques August Pi I Sunyer
EU CT number
2025-521460-36-00

What you commit to

  • Study type: Interventional · Phase 4
  • Planned participants: 120
  • 7 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of EU CTIS (euclinicaltrials.eu). It describes the study design.

AI-kivonat: who the study is looking for

Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.

The trial is looking for adult women treated for cervical cancer who had a complete response and have been sexually active in the last 12 months. It tests extra support for sexual health and lifestyle.

Age
18 years or older (women of legal age)
Sex
Women only
Disease stage
Primary cervical cancer, FIGO stage I-III (initial or locally advanced), squamous, adenocarcinoma or adenosquamous type
Earlier treatment
Treated with surgery and/or radiotherapy, with or without systemic treatment, in a gynaecological oncology unit in Spain; complete response after treatment

Main reasons for not taking part

  • Pregnancy or breastfeeding
  • Partial response after treatment
  • Fertility-sparing treatment (trachelectomy or conization)
  • Palliative treatment
  • Contraindications to vaginal estrogens

Read by machine on 9 Nov 2026.

Who cannot take part

Copied verbatim from EU CTIS (euclinicaltrials.eu) and grouped by topic. Only the trial team decides who can take part.

Age

  • Patients under 18 years of age

Other

  • Pregnancy or breastfeeding.
  • Partial response after completion of oncospecific treatment.
  • Patients with premalignant pathology.
  • Diagnosis of a tumor of non-cervical origin or atypical histologies.
  • Impossibility of completing the questionnaires included in the protocol autonomously.
  • Contraindications to the use of vaginal estrogens.
  • Patients undergoing fertility-sparing treatment (trachelectomy or conization).
  • Patients undergoing palliative treatment.

Who the study is looking for

  • Women of legal age
  • Patients with primary cervical cancer stage FIGO I-III (initial or locally advanced) of squamous histology, adenocarcinoma or adenosquamous.
  • Patients treated for cancer with surgery and/or radiotherapy ± systemic treatment in the Gynaecological Oncology Units of hospitals in Spain.
  • Complete response after oncospecific treatment was obtained.
  • Signature of the informed consent (IC) by the patient or responsible family member.
  • Patients who have been sexually active within the last 12 month

Age in the registry: 18 years to - · Sex: Female · Does not accept healthy volunteers

Full criteria on EU CTIS (euclinicaltrials.eu)

Sites (7)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Hospital Clinic de BarcelonaBarcelonaSpainRecruiting
Hospital Vall d'HebronBarcelonaSpainRecruiting
Hospital Clínico San CarlosMadridSpainRecruiting
Hospital La PazMadridSpainRecruiting
Hospital Universitario 12 de OctubreMadridSpainRecruiting
Hospital Universitario de NavarraPamplonaSpainRecruiting
Hospital Universitario Y Politecnico La FeValenciaSpainRecruiting

Are you the coordinator? Confirm the details

This page is information, not medical advice. Discuss any trial with your doctor.