ClinicalTrials.gg
Status unknownNCT03571542SPIROKIDUpdated Jun 18, 2021

Evaluation of the Respiratory Function in Renal Transplanted Children

An interventional study of pulmonary function in Respiratory Tract Disease, Kidney Transplantation and Pediatric, sponsored by Nantes University Hospital. Status unknown at 5 sites in France. Open to participants aged 2 Years to 20 Years. Per ClinicalTrials.gov, last updated 2021-06-18.

Sponsored by Nantes University Hospital · Not applicable, Interventional, and Other

The sponsor has not verified this record recently (last verified Jun 2021), so the status shown — last known as Recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
385
Allocation
Not applicable
Ages
2 Years to 20 Years
Sex
All
01

Study summary

Objectives:

While a respiratory abnormality was found in 50% of pediatric renal transplant recipients in a study conducted in Belgium and the Netherlands in 2008, the respiratory status of transplanted children in France remains unknown. The primary objective of this study is to assess the prevalence of respiratory impairment and its characteristics in children with renal transplant. The secondary objective is to study its association with some potential risk factors such as immunosuppressive therapy or humoral immunodeficiency.

Methodology:

This interventional study aims to recruit the 385 children currently being followed by 5 French pediatric renal transplant centers between June 2018 and November 2019. A clinical and functional respiratory assessment will be carried out during the routine annual follow-up of the transplant recipient. Children with clinical signs of concern or abnormal spirometry will be referred to a respiratory specialist. Pharmacokinetic assays of immunosuppressant therapy and the exploration of humoral function will also be performed. The prevalence and type of respiratory abnormalities will be described. Logistic regression will be used to explore the association between potential risk factors and impaired respiratory function.

Expected results:

This study will be the first to evaluate the respiratory status of children with renal transplants in France. The prospective, multi- centered nature of the study, in addition to the large cohort size (which represents two thirds of children with renal transplants in France) will guarantee current, reliable, and representative data for the target population. We will provide new knowledge by precisely characterizing the type of lung injury and looking for potential risk factors. If our study confirms the high prevalence of pulmonary impairment in children with renal transplants, systematic monitoring of respiratory function may be recommended to enable early diagnosis and management. The expected individual and public health benefits would be significant by limiting the appearance of long-term, irreversible sequelae (such as non-cystic-fibrosis bronchiectasis) and improving the quality of life of these patients.

02

Conditions studied

  • Respiratory Tract Disease
  • Kidney Transplantation
  • Pediatric

Keywords

  • Children
  • transplanted
  • kidney transplantation
  • respiratory function
  • pulmonary function tests
  • respiratory disease
  • immunosuppression
03

In context

Respiratory Tract Diseases

626 studies on the registry are indexed under Respiratory Tract Diseases; 115 are open to participants now.

This study's planned enrollment of 385 is above the median of 80 across 388 interventional studies indexed under Respiratory Tract Diseases.

Browse Respiratory Tract Diseases studies →

Lead sponsor

Nantes University Hospital is the lead sponsor of 837 studies on the registry; 196 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
2 Years to 20 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Renal transplanted
  • Patients of 2 to 20 years old
  • Followed in one the five centers mentionned above (Nantes, Necker, Robert Debré, Lyon, Lille)

Exclusion criteria

Exclusion Criteria:

  • Disaggrement from the patient and/or his/her legal representant
  • Impossibility to do the pulmonary function test
  • Cystic fibrosis
  • Patient with another transplant (heart, lung, liver)
05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
385 participants (estimated)

Interventions

  • Otherpulmonary function

    The aim of this study is to assess the respiratory function thanks to pulmonary function tests in renal transplanted children in France.

06

What researchers measure

Primary outcomes

  1. Respiratory alteration

    An alteration of the pulmonary function tests (PFT) values or the presence of chronic respiratory symptoms/treatment (questionnaire)

    Time frame: at the inclusion

Secondary outcomes

  1. risk factors linked to an alteration of the respiratory function

    We will analyse the relation between several exposure variables or the potential risk factors (medical past, medication, infectious diseases,...) and the presence of an alteration of the respiratory function. Clinical datas will be gathered thanks to a questionnaire on the medical past and the respiratory state of the child. The usual biological measures will be done at the annual check up (exploring immunity, pharmacological dosages, renal function, for example).

    Time frame: at the inclusion

07

Study locations

5 of 5 sites recruiting
  • CHRU Lille
    Lille, France
    • Robert NOVO · Contact
    Recruiting
  • Hospices Civiles de Lyon
    Lyon, France
    • Anne-Laure SELLIER · Contact
    Recruiting
  • CHU de Nantes
    Nantes, France
    • Alexandra BRUEL, Dr · Contact
    Recruiting
  • Hôpital Universitaire Necker Enfants Malades
    Paris, France
    • Laurène DEHOUX · Contact
    Recruiting
  • Robert Debre Hospital
    Paris, France
    • Véronique BAUDOUIN, Dr · Contact
    Recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 18, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT03571542
Collaborators
University Hospital, Lille, Hospices Civils de Lyon, Hôpital Necker-Enfants Malades, Hopital Universitaire Robert-Debre
Responsible party
Sponsor
First posted
Jun 27, 2018
Start date
Jul 16, 2018
Primary completion
Jul 16, 2022 (estimated)
Completion
Jul 16, 2022 (estimated)
Last update
Jun 18, 2021

Study contacts

Alexandra BRUEL
Contact
alexandra.bruel@chu-nantes.fr
0240083566
Tiphaine BIHOUEE
Contact
tiphaine.bihouee@chu-nantes.fr
0240083333

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Jun 2021. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion