Establishing a national cohort for juvenile recurrent respiratory papillomatosis in France
Official title: Juvenile Recurrent Respiratory Papillomatosis: Establishment of a French National Cohort (PRR : National Cohort " REPA ")
Run by Imagine Institute · NCT06000527 · Data updated 2026-11-12
This study aims to gather information about juvenile recurrent respiratory papillomatosis in children in France to understand the disease better and improve treatment options.
Quick facts
| Study type | Observational |
|---|---|
| Sex | All |
| Enrollment | 200 (estimated) |
| Sponsor | Imagine Institute Academic / other |
| Locations | 1 site (Paris) |
| Status | Recruiting |
| Started | October 1, 2022 |
| Main results expected | September 30, 2032 |
| Study ends | September 30, 2032 |
| Registry record updated | August 21, 2023 |
| Trial ID | NCT06000527 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are patients diagnosed with juvenile recurrent respiratory papillomatosis who are under 18 years of age.
✕Probably not a fit
Patients who object to the collection of their personal data will 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 observational study aims to establish the epidemiology of juvenile recurrent respiratory papillomatosis (RRP), the most common benign laryngeal tumor in children, in France. It will collect data from reference centers to better understand the disease's epidemiology, risk factors, genetic susceptibility, and clinical manifestations. The study will also evaluate the efficacy of existing therapies and preventive measures to create standardized treatment guidelines. By gathering this data, the study seeks to fill the gap in the current lack of epidemiological information on RRP in France.
Why it matters
Potential benefit: If successful, this study could lead to improved understanding and management of juvenile recurrent respiratory papillomatosis, ultimately enhancing patient care.
How similar studies have gone: While this study is focused on establishing a national cohort, similar studies in other countries have successfully gathered epidemiological data on RRP, indicating potential for success.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients with juvenile PRR (disease onset before age 18) * Followed in the : * The MALO CRMR * One of the MALO network's CCMRs * One of the main correspondent centers Exclusion Criteria: * Patients objecting to the collection of their personal data * Parents of minor patients objecting to the collection of their child's personal data
Where it's running
-
hôpital Necker Enfants malades
Paris, France Recruiting
Study contacts
- Study coordinator: Nicolas LEBOULANGER, MD
- Email: nicolas.leboulanger@aphp.fr
- Phone: 0144494682
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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Autologous dendritic cell vaccine for recurrent respiratory papillomatosis
This test tries a vaccine made from your own dendritic cells loaded with HPV6 peptides to see if it is safe and stimulates the immune system in people with HPV6-positive recurrent respiratory papillomatosis.
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Treatment of Recurrent Respiratory Papillomatosis with PRGN-2012
This study is testing a new treatment called PRGN-2012 in adults with recurrent respiratory papillomatosis to see if it helps reduce their symptoms after multiple surgeries.
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Understanding the biology of Pulmonary Recurrent Respiratory Papillomatosis
This study is collecting tissue samples from patients with Pulmonary Recurrent Respiratory Papillomatosis to better understand the disease and find new treatments.
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Pembrolizumab plus lenvatinib for HPV-related recurrent respiratory papillomatosis with lung involvement
This research will try pembrolizumab together with lenvatinib in adults who have HPV-associated recurrent respiratory papillomatosis that involves the lungs.
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Registry for patients with rare diseases
This study is creating a central registry for people with rare diseases to help connect them with researchers and improve treatments.
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.