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Recruiting Observational

Craniopharyngioma and Pregnancies

NCT06801756 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2025-03-24
Last updated
2025-04-02

Condition(s) studied

Craniopharyngioma

Investigational drug(s) / intervention(s)

Questionnaire

Questionnaire: The patients will respond to a questionnaire about their parental project, the occurence or not of complications during the pregnancy, and the impact of pregnancy on craniopharyngioma.

Study summary

Craniopharyngiomas (CP) are rare hypothalamic-pituitary tumors found in young children, adolescents and adults. The management of PC remains complex, as their aggressive nature, invasive behavior and propensity to recur require sequential and balanced therapeutic attitudes, as well as follow-up in an expert center. Although patient survival rates are high, the consequences of the tumor and its treatment can lead to serious comorbidities and impaired quality of life, particularly in patients whose tumors extend to the hypothalamus. There is very little literature describing the outcome of pregnancy in craniopharyngioma patients and its impact on the craniopharyngioma. The largest study describes 6 women, mean age 24, who had a craniopharyngioma in childhood. Half of them had induced pregnancies; there is a succinct description of pregnancy complications and outcomes, as well as tumor progression.

In the endocrinology department of Pitié Salpêtrière hospital, the investigators regularly follow over a hundred patients of all ages who have presented with a craniopharyngioma in childhood or adulthood. They are also unique in having a medically assisted reproduction unit, which helps couples to realize their parental project. This dual specialization will enable to describe pregnancies and their impact on the behavior of craniopharyngiomas.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patients aged at least 18 years old * Patients with or having had a craniopharyngioma * Patients informed and not opposed to participation in research Exclusion Criteria: * Patients who don't speak french * Patients without medical care insurance * Patients under legal protection

Primary outcome measure(s)

  • Describe how pregnancies are obtained: spontaneous or induced (and by which assisted reproduction technique). — 12 months
    Information on how the pregnancy was obtained will be collected from the medical record and will be completed on the day of inclusion by a telephone questionnaire with the patient.

Trial sites (1)

FacilityCityRegionStatus
Pitié-Salpêtrière hospital Paris France Recruiting

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06801756 on ClinicalTrials.gov ↗ ← All trials in France