Biodegradable Airway Stent Post Lung Transplant

Sponsor
University Medical Center Groningen (Other)
Overall Status
Completed
CT.gov ID
NCT05334199
Collaborator
AIDS Malignancy Consortium (Other)
20
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1
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10
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Study Details

Study Description

Brief Summary

Introduction and rationale

Benign airway stenosis or malacia is a frequent complication of lung transplantation occurring in 4-24% of patients, most often occurring two to nine months post-transplant. Initial therapeutic approach consists of conservative endobronchial treatment with recurrent balloon dilatation, radial incision, and electro cautery. For severe case of recurrent stenosis or malacia, airway stent placement can be considered. Different types of airway stent exist, for instance self-extendable metallic stent (SEMS), silicone stent and biodegradable airway stent. Conventional airway stents (SEMS, silicone) are associated with complications as granulation tissue and recurrent infections and can be difficult to remove. Newly developed biodegrabale stents are made of polydioxanone and disintegrate after a period of time are thought to have less side effects, and has been standard of care for the last few years. A sub selection of patients have been treated with conventional stent before treated with biodegradable stent.

Research question

  • To assess the efficacy and efficiency of biodegradable airway stent.

  • Compare occurrence of adverse events such as infection, dislocation, in stent granulation and difficulty of removal to conventional metallic or silicone stents.

  • Asses if biodegradable stent lead to improvement of lung function.

  • Assessment of the life span of biodegradable stents.

Condition or Disease Intervention/Treatment Phase
  • Device: Biodegradable stent
N/A

Detailed Description

  • Background Recurrent airway stenosis or malacia can be treated with airway stents. Conventional airway stents, for instance self-extendable metallic stent (SEMS) and silicone stent are associated with adverse events as recurrent infection or granulation tissue and can be difficult to remove because of in stent-granulation. Therefore they are used with restraint for benign airway problems. Biodegradable stents are made of polydioxanone and disintegrate after a period of time. They are thought to be well tolerated and associated with less adverse events compared to traditional airway stent and have been used as standard care for multiple years.

  • Main research question

  • To assess the efficacy and efficiency of biodegradable airway stent

  • Compare occurrence of adverse events such as infection, dislocation, in stent granulation and difficulty of removal to conventional metallic or silicone stents.

  • Asses if biodegradable stent lead to improvement of lung function.

  • Assessment of the life span of biodegradable stents.

  • Design (including population, confounders/outcomes) Retrospective cohort study of patients with airway stenosis or malacia treated with biodegradable airway stent from 2019 in the UMCG and Amsterdam UMC.

  • Expected results

  • Less adverse events, hospital admittance and need for bronchoscopic interventions compared to patients treated with conventional stents. No complications associated with removal of stents.

  • Life span around 4 months

Study Design

Study Type:
Interventional
Actual Enrollment :
20 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Evaluation of Treatment With Biodegradable Airway Stent for Post Lung Transplant Airway Complication
Actual Study Start Date :
Apr 2, 2019
Actual Primary Completion Date :
Mar 31, 2022
Actual Study Completion Date :
Mar 31, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Biodegradable stent treatment group

Biodegradable stent treatment group

Device: Biodegradable stent
Bronchoscopic placement of biodegradable stent in patients with airway complications after lung transplant

Outcome Measures

Primary Outcome Measures

  1. Adverse events [4 months after placement]

    Adverse events associated with airway stents

Secondary Outcome Measures

  1. Change in FEV1 [1 week post placement]

    Change in FEV1 measured by spirometry pre and post stent placement

  2. Change in FVC [1 week post placement]

    Change in FVC measured by spirometry pre and post stent placement

  3. Time to need for new stent placement [6 months after placement]

    Endurance and life span of biodegradable stent measured by time to need for new stent placement

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patients who underwent a lung transplantation and developed airway stenosis or malacia with airway stent requirement
Exclusion Criteria:
  • No

Contacts and Locations

Locations

Site City State Country Postal Code
1 AMC Amsterdam Netherlands
2 UMCG Groningen Netherlands

Sponsors and Collaborators

  • University Medical Center Groningen
  • AIDS Malignancy Consortium

Investigators

  • Principal Investigator: Dirk-Jan Slebos, MD, PhD, UMCG

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Dirk-Jan Slebos, Prof. dr., University Medical Center Groningen
ClinicalTrials.gov Identifier:
NCT05334199
Other Study ID Numbers:
  • 20220075
First Posted:
Apr 19, 2022
Last Update Posted:
Apr 27, 2022
Last Verified:
Apr 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Apr 27, 2022