Evaluation of follow-up care for adults with esophageal atresia
Official title: Evaluation Prospective Des résultats du Suivi Pluridisciplinaire Mis en Place au décours d'Une Consultation de Transition Pour l'atrésie de l'œsophage
Run by Assistance Publique - Hôpitaux de Paris · NCT06860919 · Data updated 2026-11-12
This study is testing a new follow-up care program for adults with esophageal atresia to see if it helps improve their overall quality of life and manage issues like PTSD.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years to 30 Years |
| Sex | All |
| Enrollment | 50 (estimated) |
| Sponsor | Assistance Publique - Hôpitaux de Paris Academic / other |
| Locations | 1 site (Paris) |
| Status | Recruiting |
| Started | December 19, 2024 |
| Main results expected | December 19, 2030 |
| Study ends | December 19, 2030 |
| Registry record updated | March 6, 2025 |
| Trial ID | NCT06860919 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are adults aged 18 to 30 who have been diagnosed with esophageal atresia and are receiving care at Hôpital Saint-Louis.
✕Probably not a fit
Patients who are unable to complete questionnaires or are under guardianship may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study evaluates the outcomes of a multidisciplinary follow-up program for adult patients with esophageal atresia initiated at Hôpital Saint-Louis. The program aims to provide comprehensive medical, psychological, and social support while empowering patients to manage their own care. Over a three-year period, the study will analyze various somatic and psychosocial factors to assess the effectiveness of this initiative in improving the quality of life for these individuals. It is the first to specifically address post-traumatic stress disorder (PTSD) in this patient population.
Why it matters
Potential benefit: If successful, this initiative could significantly enhance the quality of life and care management for adults with esophageal atresia.
How similar studies have gone: This approach is novel and has not been extensively tested in similar studies, particularly regarding PTSD in young adults with esophageal atresia.
Who can join: the full rules
Show full inclusion / exclusion criteria
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)
Where it's running
-
Hopital Saint Louis
Paris, France Recruiting
Study contacts
- Study coordinator: Pierre Cattan, MD PhD
- Email: pierre.cattan@aphp.fr
- Phone: 142499381
Similar studies
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The study will see if parents who learn about their baby's esophageal atresia before birth have different levels of post‑traumatic reactions than parents who learn after birth, focusing mainly on mothers (with fathers invited to participate) of children aged 12–24 months who had neonatal surgery.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.