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Clinical Trials in France / NCT06860919
Recruiting Observational

Prospective Evaluation of the Results of Multidisciplinary Follow-up After a Transitional Consultation for Esophageal Atresia

NCT06860919 · tracked via the Priya Life Science France tracker
Sponsor
Assistance Publique - Hôpitaux de Paris
Phase
Observational
Started
2024-12-19
Last updated
2025-03-06

Condition(s) studied

Esophageal Atresia

Investigational drug(s) / intervention(s)

Follow-up of the patients during 3 years

Follow-up of the patients during 3 years: Evaluation of PTSD prevalence, anxiety-depressive state, quality of life, look for a correlation between their clinical history and PTSD. Analysis of the nutritional, gastrointestinal and respiratory status.

Study summary

A transition consultation for adult patients with esophageal atresia, involving medical and paramedical stakeholders, was set up at Hôpital Saint-Louis in 2020. The aim of this initiative is to: 1. initiate adult medical, psychological and social follow-up; 2. empower these adults in their future care; 3. establish a personalized follow-up schedule. This project is the first to focus on post-traumatic stress disorder (PTSD) in young adults with esophageal atresia. A 3-year analysis of the somatic and psychosocial variables analyzed will confirm the validity of this initiative, and define its optimal contours for improving these patients' quality of life as adults.

Eligibility

Sex
ALL
Min age
18 Years
Max age
30 Years
Healthy volunteers
No
Inclusion Criteria: * Patients with esophageal atresia * Aged 18 to 30 * Followed at Hôpital Saint Louis * Informed and not opposed to the study * Patients affiliated to a social security scheme Exclusion Criteria: * Inability to answer questionnaires * Patients under guardianship * Patients under AME (Aide Médicale d'Etat in France)

Primary outcome measure(s)

  • Prevalence of Post Traumatic Stress Disorder — At day 0

Trial sites (1)

FacilityCityRegionStatus
Hopital Saint Louis Paris France Recruiting

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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 NCT06860919 on ClinicalTrials.gov ↗ ← All trials in France