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Gonadal Toxicity in Women With Hodgkin Lymphoma

Observational Retrospective Study to Evaluate the Incidence of the Gonadal Toxicity in Women of Reproductive Age With Hodgkin Lymphoma

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01008735
Acronym
FertHD
Enrollment
150
Registered
2009-11-06
Start date
2009-07-31
Completion date
Unknown
Last updated
2009-11-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hodgkin Lymphoma

Brief summary

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.

Interventions

None listed

Sponsors

Gruppo Italiano Studio Linfomi
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 40 Years
Healthy volunteers
No

Inclusion criteria

* 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 * No other chemo-radiotherapy for other neoplasm * Written informed consent

Exclusion criteria

* none

Design outcomes

Primary

MeasureTime frame
incidence of gonadal toxicity in terms of irreversible amenorrhea and infertility, in women of reproductive age with Hodgkin lymphoma treated with chemotherapy.from end of treatment until date of last contact/visit

Secondary

MeasureTime frame
role of a prophylactic treatment with oral contraceptives and GnRH analogs in preventing gonadal damagefrom end of treatment until date of last contact/visit

Countries

Italy

Contacts

Primary ContactAntonella Montanini, BSc, PhD
amontanini@unimore.it\+39 059 4223284

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026