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Anti-mullerian Hormone in Acute Lymphoblastic Leukemia

Anti-mullerian Hormone in Pediatric Patients Treated for Acute Lymphoblastic Leukemia

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05793463
Enrollment
10
Registered
2023-03-31
Start date
2018-02-15
Completion date
2024-03-15
Last updated
2023-03-31

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

Conditions

Acute Lymphoblastic Leukemia

Keywords

Acute Lymphoblastic Leukemia, Fertility preservation, Anti-Mullerian hormone

Brief summary

Acute lymphoblastic leukemia (ALL) is the most common childhood malignancy, with current survival rates exceeding 90%. As cure rates improve, increasing attention is focused on survivor quality of life, including fertility. It is generally accepted that cancer treatments in childhood may interfere with gonadal function, reducing the pool of primordial follicles and consequently causing premature menopause in women. Anti-Mullerian hormone (AMH) levels is a valuable quantitative indicator of ovarian reserve, being directly related to the number of antral follicles. The evaluation of this hormone makes it possible to identify women at risk of early menopause and to propose them interventions for monitoring and preservation of oocytes, allowing girls to be able to have children once they reach adulthood. The objective of this study is to determine ovarian reserve in girls with ALL before and after treatment by means of the evaluation of the AMH assay.

Interventions

None listed

Sponsors

IRCCS Burlo Garofolo
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
1 Months to 18 Years
Healthy volunteers
No

Inclusion criteria

* Female less than 18 years of age * Diagnosis of acute lymphoblastic leukemia * enrollment within the first month after diagnosis

Exclusion criteria

* Previous treatments with cytostatics drugs * ALL as a second malignancy * Syndromic patient or primary hypogonadism

Design outcomes

Primary

MeasureTime frameDescription
Evaluation of blood AMH levels before ALL treatmentWithin one months from ALL diagnosisAMH levels will be evaluated in peripheral blood
Evaluation of blood AMH levels after ALL treatment24 months after ALL diagnosisAMH levels will be evaluated in peripheral blood

Countries

Italy

Contacts

Primary ContactNagua Giurici, MD
nagua.giurici@burlo.trieste.it+390403785342

Outcome results

None listed

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