Gonadal Toxicity in Women With Hodgkin Lymphoma (FertHD)
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ClinicalTrials.gov Identifier: NCT01008735
Recruitment Status : Unknown
Verified November 2009 by Gruppo Italiano Studio Linfomi. Recruitment status was: Recruiting
The Gruppo Italiano Studio Linfomi has been collecting data on patients with Hodgkin Lymphoma (HL) since 1988. This archive represents a homogeneous series of consecutive patients with HL. The very long follow up and the availability of clinical and treatment data make it feasible to perform a study on the gonadal toxicity related to treatment for HL.
incidence of gonadal toxicity in terms of irreversible amenorrhea and infertility, in women of reproductive age with Hodgkin lymphoma treated with chemotherapy. [ Time Frame: from end of treatment until date of last contact/visit ]
Secondary Outcome Measures :
role of a prophylactic treatment with oral contraceptives and GnRH analogs in preventing gonadal damage [ Time Frame: from end of treatment until date of last contact/visit ]
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Layout table for eligibility information
Ages Eligible for Study:
18 Years to 40 Years (Adult)
Sexes Eligible for Study:
Accepts Healthy Volunteers:
Female patients with Hodgkin lymphoma diagnosed until 2007 in Italy will be considered eligible for this study. Cases will be identified from the archives of GISL.
Female patients in complete remission after chemotherapy for Hodgkin lymphoma
Age ≥ 18 e < 40 years
Previous regular menstrual cycle
No previous or concomitant gynecological diseases affecting reproducing function