Actively Recruiting
Description of Pregnancies and Their Impact on Craniopharyngioma in Women
Led by Assistance Publique - Hôpitaux de Paris · Updated on 2025-04-02
100
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Craniopharyngiomas are rare, benign tumors that develop near the pituitary gland and mostly affect children, adolescents, and adults. These tumors can cause serious health issues due to their invasive nature and tendency to recur, impacting quality of life through hormonal, vision, and cognitive problems. There is limited information about pregnancy outcomes and effects on craniopharyngiomas in women who have had these tumors, which this study aims to explore. This research involves patients who have or had craniopharyngiomas and focuses on describing pregnancies and their impact on tumor behavior. Participants will complete questionnaires about their parental projects, pregnancy complications, and the tumor's response during and after pregnancy. The study is observational and conducted at a specialized center with expertise in endocrine and reproductive health. Participants will provide information through questionnaires supplemented by medical records. Researchers will assess how pregnancies were achieved, hormonal treatment adjustments, tumor changes, visual and neurocognitive effects, and weight changes during pregnancy. The study will last about one year, with each participant's involvement around thirty minutes. Outcomes will help understand pregnancy's role in craniopharyngioma management and patient care.
CONDITIONS
Brief Title
Craniopharyngioma and Pregnancies
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients aged at least 18 years old
- Patients with or having had a craniopharyngioma
- Patients informed and not opposed to participation in research
You will not qualify if you...
- Patients who don't speak French
- Patients without medical care insurance
- Patients under legal protection
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person or remote)
Duration - Up to 12 months
Participants complete questionnaires about their pregnancy history, complications, and the impact of pregnancy on craniopharyngioma. Medical records are reviewed to supplement questionnaire data.
1 telephone contact to complete questionnaire
Trial Site Locations
Total: 1 location
1
Pitié-Salpêtrière hospital
Paris, France, 75013
Actively Recruiting
Research Team
A
Anne BACHELOT, MD, PhD
Z
Zeina Chakhtoura, MD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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