Skip to main content
Clinical Trials/NCT03418844
NCT03418844
Active, not recruiting
Not Applicable

Living After a Rare Cancer of the Ovary: Chronic Fatigue, Quality of Life and Late Effects of Chemotherapy

Centre Francois Baclesse19 sites in 1 country268 target enrollmentMay 7, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Germ Cell Tumor
Sponsor
Centre Francois Baclesse
Enrollment
268
Locations
19
Primary Endpoint
The quality of life by questionnaires
Status
Active, not recruiting
Last Updated
7 months ago

Overview

Brief Summary

While they are documented in patients in remission of testicular cancer, the sequelae of chemotherapy and the impact of the disease and its treatments on the living conditions and QoL of women in remission of rare ovarian cancer remain poorly explored.

The coordinator therefore propose a national 2-step case-control study to evaluate 1) chronic fatigue and QoL and 2) chemotherapy-related sequelae in adult patients in remission of surgery-treated TGMO or TSCS (conservative or not) supplemented with chemotherapy

Registry
clinicaltrials.gov
Start Date
May 7, 2018
End Date
December 1, 2025
Last Updated
7 months ago
Study Type
Interventional
Study Design
Single Group
Sex
Female

Investigators

Sponsor
Centre Francois Baclesse
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Age\> 18 years;
  • Patient with an ovarian malignant germ cell tumor (TGMO) or a stroma tumor and / or sex cords (TSCS) treated optimally;
  • Patient who has had surgery and chemotherapy (interest group) or only a surgery (control group);
  • Patient in remission more than 2 years after the end of the initial treatment;
  • Relapse authorized if remission more than 2 years after the end of the treatment;
  • Patient with no other cancers (with the exception of basal cell skin carcinomas, in situ cancers of the breast and cervix);
  • Patient having signed his consent to participate

Exclusion Criteria

  • Pregnant or breastfeeding woman;
  • Psychiatric pathology that may disrupt the course of the study or prevent the interpretation of results;
  • Person deprived of liberty;
  • Major subject to a legal protection measure or unable to express his consent.

Outcomes

Primary Outcomes

The quality of life by questionnaires

Time Frame: 2 years after surgery

The late sequelae of chemotherapy, particularly cardiovascular and pulmonary disorders, in adult patients in remission of a rare cancer of the ovary treated by surgery, supplemented or not by chemotherapy.

Time Frame: 2 years after surgery

The chronic fatigue by questionnaires

Time Frame: 2 years after surgery

Secondary Outcomes

  • The symptoms of menopause by questionnaires(2 years after surgery)
  • Theimpact of cancer and its treatments on the trajectory and professional situation by questionnaires(access to work, professional ambition, financial situation ...);(2 years after surgery)
  • The fertility monitoring by questionnaires(2 years after surgery)
  • The parental projects by age (≤ 45 years) by questionnaires(2 years after surgery)

Study Sites (19)

Loading locations...

Similar Trials