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Идёт набор NCT05616325

Long-term Ovarian Fertility in Patients Treated for Lymphoma.

Наблюдательное Lymphoma, Follicular

Ориентир для пациента и семьи

Простыми словами

Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.

Что изучают
Это наблюдательное исследование: исследуемое лечение участникам по протоколу не назначают.
Кому может быть актуально
Состояния в реестре: Lymphoma, Follicular. Базовые параметры: 18 лет — 45 лет · Женщины.
Что важно проверить
Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
Где проводится
Франция
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

Long-term Follow-up of Ovarian Function and Fertility in Young Lymphoma Patients Treated by Chemotherapy

Обзор

This is an observational, single-center, longitudinal cohort study. In order to evaluate the gonadotoxicity of chemotherapy, an AMH monitoring was initiated in 2006 in our fertility observatory in young patients with lymphoma before, during and after chemotherapy. This study is part of the project "She will get better and then want a child" and is supported by the ARS hauts de France (n° DOS/SDES/AR/FIR/2019/282). Our first study published in 2010 shows that AMH decreases sharply during chemotherapy, regardless of the chemotherapy protocol. At the end of chemotherapy, AMH recovery profiles differ according to the protocol received. This follow-up is therefore essential in order to adapt our practices and our preservation strategies, particularly to the type of chemotherapy. Patients are primarily concerned about their chances of subsequent pregnancy, and there is little evidence in the literature about the impact of chemotherapy on ovarian reserve and long-term fertility. The fisrt objective of our study is to evaluate, at distance from chemotherapy, the evolution of ovarian function in patients treated for lymphoma by evaluating follicular reserve parameters (AMH and antral follicle count) at 5 and 10 years after the end of chemotherapy compared with the initial workup performed before chemotherapy and the workup performed at 12 months after the end of chemotherapy.

Первичные конечные точки

  • Follicular reserve parameters (AMH and antral follicle count) [Срок оценки: at the end of chemotherapy]
Вторичные конечные точки (7)
  • Cumulative incidence of pregnancy at 5 years and 10 years from the end of treatment defined by the achievement of at least one spontaneous or induced pregnancy. [Срок оценки: at 5 and 10 years after the end of chemotherapy.]
  • Pregnancy rate obtained by ART (with or without gamete reuse) [Срок оценки: at 5 and 10 years after the end of chemotherapy.]
  • Rate of miscarriages, ectopic pregnancies, and live births (single, multiple) [Срок оценки: at 5 and 10 years after the end of chemotherapy.]
  • Scores on the Reproductive Concerns (RCACS) [Срок оценки: at 5 and 10 years after the end of chemotherapy.]
  • Scores Mood (PHQ) [Срок оценки: at 5 and 10 years after the end of chemotherapy.]
  • Quality of Life (FACT-G7) [Срок оценки: at 5 and 10 years after the end of chemotherapy.]
  • Life Satisfaction (SWLS) scales [Срок оценки: at 5 and 10 years after the end of chemotherapy.]

Критерии участия

Критерии включения

  • Patients with a history of lymphoma treated with chemotherapy
  • followed in the fertility observatory of the Jeanne de Flandre Hospital at the University Hospital of Lille (project "she will heal and then want a child"), who are at least at 5 years since the end of chemotherapy
  • Patients having been informed and having given their written consent to participate in the study.
  • Beneficiary of a social security system.

Критерии исключения

  • Patient not followed in the fertility observatory.
  • Inability of the patient to undergo the medical follow-up of the trial for geographical, social or psychological reasons.
  • Patient opposed to her participation in the study.
  • Patient under guardianship or curatorship.

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Модель наблюдения
Когортное

Центры проведения

Франция · 1 центр
  • chu de Lille — Lille

Идентификаторы

NCT: NCT05616325 · 2022_0072 · 2022-A01753-40

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗