Understanding pregnancy outcomes in craniopharyngioma patients
Description of Pregnancies and Their Impact on the Craniopharyngioma
This study looks at how pregnancy affects people with craniopharyngioma, a rare brain tumor, by gathering experiences from those who have been diagnosed or treated for it.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 100 (estimated) |
| Ages | 18 Years and up |
| Sex | Female |
| Sponsor | Assistance Publique - Hôpitaux de Paris Academic / other |
| Locations | 1 site (Paris) |
| Trial ID | NCT06801756 on ClinicalTrials.gov |
What this trial studies
This observational study aims to explore the outcomes of pregnancy in patients with craniopharyngioma, a rare type of brain tumor. It will involve collecting data through questionnaires from individuals aged 18 and older who have been diagnosed with or treated for craniopharyngioma. The study seeks to fill the gap in existing literature regarding the impact of pregnancy on tumor progression and patient health. By analyzing the experiences of these patients, the research hopes to provide insights into the management of pregnancies in this unique population.
Who should consider this trial
Good fit: Ideal candidates for this study are women aged 18 and older who have been diagnosed with or treated for craniopharyngioma.
Not a fit: Patients who do not speak French or those without medical care insurance may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could improve the understanding of pregnancy-related risks and outcomes for patients with craniopharyngioma, leading to better management strategies.
How similar studies have performed: There is limited literature on this topic, making this study a novel exploration of pregnancy outcomes in craniopharyngioma patients.
Eligibility criteria
Show full inclusion / exclusion criteria
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
Where this trial is running
Paris
- Pitié-Salpêtrière hospital — Paris, France (Recruiting)
Study contacts
- Study coordinator: Anne BACHELOT, MD, PhD
- Email: anne.bachelot@aphp.fr
- Phone: 01 42 16 02 46
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.