Airway Intervention Registry (AIR): Recurrent Respiratory Papillomatosis (RRP) (AIR:RRP)
Airway Intervention Registry (AIR) Extension: Recurrent Respiratory Papillomatosis
Sponsor: Alder Hey Children's NHS Foundation Trust
A observational or N/A phase clinical study on Human Papilloma Virus and Recurrent Respiratory Papillomatosis, this trial is ongoing. The trial is conducted by Alder Hey Children's NHS Foundation Trust and has accumulated 26 data snapshots since 2018. Longitudinal tracking of this trial contributes to a broader understanding of treatment development timelines.
Study Description(click to expand)Primary aim: The overall goal is to improve the care of patients with Recurrent Respiratory Papillomatosis (RRP) - and the investigators aim to do this by determining the most effective and safe RRP treatments currently being used in patients in National Health Service (NHS) hospitals within the United Kingdom (UK) (information which is currently lacking). By determining the most effective treatments of RRP, the investigators will be able to increase the time interval between surgical interventions to maintain symptomatic control, reduce overall number of RRP interventions, severity and spread of papillomas in the airway, hospital visits, medications and ultimately improve quality of life in those suffering from RRP. By also capturing peri- and post-procedural details the investigators will be able to determine the relative safety of treatments and identify those which slow the progression of disease. From the data collected the investigators intend to identify patient subgroups (based on patient characteristics such as age, gender, human papillomavirus (HPV) type, location of papillomas, RRP severity and spread, comorbidities) who respond better to specific treatments, and also identify patient risk factors which contribute to the complication outcomes (such as tracheostomy). Secondary aims: * build an evidence base of the different RRP treatments...
Primary aim:
The overall goal is to improve the care of patients with Recurrent Respiratory Papillomatosis (RRP) - and the investigators aim to do this by determining the most effective and safe RRP treatments currently being used in patients in National Health Service (NHS) hospitals within the United Kingdom (UK) (information which is currently lacking).
By determining the most effective treatments of RRP, the investigators will be able to increase the time interval between surgical interventions to maintain symptomatic control, reduce overall number of RRP interventions, severity and spread of papillomas in the airway, hospital visits, medications and ultimately improve quality of life in those suffering from RRP. By also capturing peri- and post-procedural details the investigators will be able to determine the relative safety of treatments and identify those which slow the progression of disease.
From the data collected the investigators intend to identify patient subgroups (based on patient characteristics such as age, gender, human papillomavirus (HPV) type, location of papillomas, RRP severity and spread, comorbidities) who respond better to specific treatments, and also identify patient risk factors which contribute to the complication outcomes (such as tracheostomy).
Secondary aims:
* build an evidence base of the different RRP treatments used across the UK which will help to formulate hypotheses for future research in RRP and improve quality of life for RRP patients; * inform National Institute for Health and Care Excellence (NICE) interventional procedure guidance on radiofrequency cold ablation (IPG434,2012), which is currently under special arrangements due to lack of safety and efficacy evidence; * identify common symptoms or signs associated with RRP disease profile, to aid future diagnosis of RRP; * determine the geographical spread of RRP patients across the UK, to inform effective use of future NHS resources and inform the Department of Health strategy in its quadrivalent HPV vaccination programme (protecting against four types of HPV including types 6 and 11 commonly associated with RRP) currently offered to 12-13 year old girls within the NHS childhood vaccination programme; * inform future development of national clinical guidance on management of RRP to ensure that everyone receives the best care based on best available current knowledge; * determine impact of COVID on RRP patients including changes to RRP management, RRP symptoms.
Objectives:
The investigators will make use of an existing secure online database platform (the Airway Intervention Registry, AIR - developed and hosted by The Newcastle upon Tyne Hospitals NHS Foundation Trust, NUTH) and its associated infrastructure and develop it to capture additional observational outcomes from standard clinical practice and quality of life questionnaires from RRP patients. All RRP patients (any age) receiving treatment in any UK NHS hospital will be eligible for inclusion. Data collection will be open for 53 months with no minimum follow-up required for patients. Due to its recurrent nature (requiring regular hospital visits to maintain an open airway), following this patient population will allow the investigators to determine both the short- and long-term relative safety and efficacy of RRP treatments used in the UK. Consent will be required (from patients/parent/guardian) before data are entered into the online database.
Status Flow
Change History
26 versions recorded-
Sep 2025 — Present [monthly]
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Sep 2024 — Sep 2025 [monthly]
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Jul 2024 — Sep 2024 [monthly]
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Status: Unknown Status → Unknown
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Feb 2024 — Jul 2024 [monthly]
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Status: Recruiting → Unknown Status
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Feb 2022 — Feb 2024 [monthly]
Recruiting
▶ Show 21 earlier versions
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Sep 2021 — Feb 2022 [monthly]
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Jan 2021 — Sep 2021 [monthly]
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Oct 2020 — Jan 2021 [monthly]
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Dec 2018 — Jan 2019 [monthly]
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Nov 2018 — Dec 2018 [monthly]
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Oct 2018 — Nov 2018 [monthly]
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Jul 2018 — Aug 2018 [monthly]
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May 2018 — Jun 2018 [monthly]
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Status: Not Yet Recruiting → Recruiting
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Apr 2018 — May 2018 [monthly]
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Phase: NA → None
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Mar 2018 — Apr 2018 [monthly]
Not Yet Recruiting NA
First recorded
Eligibility Summary
No eligibility information available.
Contact Information
- Alder Hey Children's NHS Foundation Trust
- National Institute for Health Research, United Kingdom
- Newcastle-upon-Tyne Hospitals NHS Trust
For direct contact, visit the study record on ClinicalTrials.gov .