Study identifier: NCT07727824 Synced from ClinicalTrials.gov · August 05, 2026
● Not Yet Recruiting

Endoscopic Treatment

Condition: Stenoses · Dyspnea  ·  Sponsor: University Hospital, Toulouse

PhaseNA
Planned participants96
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The placement of an endoprosthesis in the airways leads to rapid and dramatic clinical improvement in the majority of cases of central airway obstruction. However, the limited diversity of device shapes available on the market is a major limitation, as these devices are poorly adapted, or not adapted at all, to the patient's anatomy. The main consequences of this lack of congruity are stent migration and granulomatous inflammatory reactions. The investigators hypothesized that personalized endoprostheses could significantly reduce the complication rate and improve tolerability. In this randomized controlled trial, the investigators propose to evaluate whether personalized endoprostheses allow for better management of non-malignant central airway stenoses by comparing this new approach to standard care.

This description comes directly from the study's public registry record.

Talk to the study team

Audrey TOMASIK  ·  +33 (0) 5 61 77 85 97  ·  tomasik.a@chu-toulouse.fr

Always discuss trial participation with your own doctor first.

Locations (6)

Hôpital Marie Lannelongue / Institut Gustave RoussyLe Plessis-Robinson, France
Institut Cœur Poumon - CHU LilleLille, France
CHU LimogesLimoges, France
CHRU StrasbourgStrasbourg, France
Hôpital FochSuresnes, France
Larrey HospitalToulouse, France

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