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Role of a Silicone Prosthesis to Prevent Airway Obstruction Recurrence in Lung Cancers (SPOC)

Primary Purpose

Lung Neoplasm, Carcinoma, Non-Small-Cell Lung

Status
Terminated
Phase
Phase 4
Locations
France
Study Type
Interventional
Intervention
silicone trachea-bronchial stent Dumon (Novatech)
Sponsored by
Centre Hospitalier Universitaire de Saint Etienne
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Lung Neoplasm focused on measuring tumoral obstruction of the main stem bronchus, bronchoscopy, silicone stent

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • > 18 years
  • non-small cell lung cancer,
  • inoperable and location : tracheal, carinal, main bronchus right or left, or intermediate trunk.
  • TNM stage known and oncological treatment later determined
  • central initial intrinsic bronchial obstruction > 50%.
  • resection of tumor with endoscopy, to obtain after therapeutic bronchoscopy a diameter > 50% normal diameter of bronchial segment achieved.
  • Tumoral segment fully recoverable by a stent
  • Written consent, free and informed
  • Patient affiliated or who is entitled to to a social security scheme.

Exclusion Criteria:

  • against-indication for general anesthesia.
  • Patient with one lung not working beyond the stenosis
  • Patient under guardianship
  • Pregnancy
  • 12 months follow-up impossible

Sites / Locations

  • Department of pneumology, CHU Amiens
  • Departement of pneumology, CHU Brest
  • Pneumology departement, Hôpital Percy
  • Pneumology departement, CHRU Lille
  • Pneumology departement, CHU Limoges
  • Pneumology departement, Sainte Marguerite hospital
  • Pneumology departement, CHU Nantes
  • Pneumology departement, Saint-Antoine hospital
  • Department of respiratory diseases and allergic, Thoracic Oncology, CHU Reims
  • Pneumology Clinic - Albert Calmette hospital- CHU Rouen
  • Pneumology departement CHU Saint-Etienne
  • Endoscopy unit, Thoracic surgery department, Foch Hospital
  • Departement of pneumology, CHU TOULOUSE

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

trachea-bronchial stent (Novatech)

control

Arm Description

Outcomes

Primary Outcome Measures

Death and / or symptomatic recurrence (proved on bronchoscopy with more than 50% of obstruction in the treated zone)

Secondary Outcome Measures

death
For patients who had no symptomatic recurrence of bronchial obstruction Presence of a bronchial stenosis> 50% on a systematic bronchial endoscopy months.
Complications of symptomatic trachea-bronchial prosthesis (mobility or migration, granuloma, congestion) motivating endoscopy.
Quality of life : EORTC

Full Information

First Posted
February 2, 2010
Last Updated
July 27, 2015
Sponsor
Centre Hospitalier Universitaire de Saint Etienne
Collaborators
Ministry of Health, France, Ligue contre le cancer, France
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1. Study Identification

Unique Protocol Identification Number
NCT01064050
Brief Title
Role of a Silicone Prosthesis to Prevent Airway Obstruction Recurrence in Lung Cancers
Acronym
SPOC
Official Title
Role of a Silicone Prosthesis to Prevent Airway Obstruction Recurrence After Therapeutic Bronchoscopy in Lung Cancers (SPOC Study)
Study Type
Interventional

2. Study Status

Record Verification Date
July 2015
Overall Recruitment Status
Terminated
Why Stopped
Difficulty to include patient
Study Start Date
November 2008 (undefined)
Primary Completion Date
May 2012 (Actual)
Study Completion Date
May 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Centre Hospitalier Universitaire de Saint Etienne
Collaborators
Ministry of Health, France, Ligue contre le cancer, France

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
A tumoral obstruction of the main stem bronchus is frequently observed in the follow-up of lung cancers with a high impact on survival and quality of life of these patients. The endoluminal resection of these tumors through interventional bronchoscopy can remove the tumor but fails to prevent the recurrence. A stent insertion could achieve this goal but this option was never proved in a prospective protocol. The aim of this study is to analyze the impact of stent insertion on the survival without symptoms of bronchial obstruction in patients treated for their cancer with and without a first line treatment (chemo-radiotherapy or chemotherapy). The patients will be included after resection of the endoluminal symptomatic tumoral obstruction. We will test the effect of the silicone stent insertion ( from NovatechR ) by comparing a stent arm (170 patients with stent insertion) with a control arm (170 patients without stent). The inclusion period will last 3 years with one year of follow-up for each patient. The one-year survival without symptomatic recurrence (proved on bronchoscopy with more than 50% of obstruction in the treated zone) will be the main endpoint. All patients without symptomatic recurrence at one year will be controlled endoscopically. Survival and stent tolerance will be studied as secondary endpoints. All endoscopic events will be depicted on photographs or videos. Each endoscopical situation (before and after resection, recurrence or side effects of stents) will be analyzed and registered by an independent committee of 3 international experts.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Lung Neoplasm, Carcinoma, Non-Small-Cell Lung
Keywords
tumoral obstruction of the main stem bronchus, bronchoscopy, silicone stent

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
75 (Actual)

8. Arms, Groups, and Interventions

Arm Title
trachea-bronchial stent (Novatech)
Arm Type
Experimental
Arm Title
control
Arm Type
No Intervention
Intervention Type
Device
Intervention Name(s)
silicone trachea-bronchial stent Dumon (Novatech)
Intervention Description
Bronchial desobstruction under interventional bronchoscopy, for inclusion, with the insertion of silicone stent trachea-bronchial covering the entire tumor area
Primary Outcome Measure Information:
Title
Death and / or symptomatic recurrence (proved on bronchoscopy with more than 50% of obstruction in the treated zone)
Time Frame
12 months
Secondary Outcome Measure Information:
Title
death
Time Frame
12 months
Title
For patients who had no symptomatic recurrence of bronchial obstruction Presence of a bronchial stenosis> 50% on a systematic bronchial endoscopy months.
Time Frame
12 months
Title
Complications of symptomatic trachea-bronchial prosthesis (mobility or migration, granuloma, congestion) motivating endoscopy.
Time Frame
12 months
Title
Quality of life : EORTC
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: > 18 years non-small cell lung cancer, inoperable and location : tracheal, carinal, main bronchus right or left, or intermediate trunk. TNM stage known and oncological treatment later determined central initial intrinsic bronchial obstruction > 50%. resection of tumor with endoscopy, to obtain after therapeutic bronchoscopy a diameter > 50% normal diameter of bronchial segment achieved. Tumoral segment fully recoverable by a stent Written consent, free and informed Patient affiliated or who is entitled to to a social security scheme. Exclusion Criteria: against-indication for general anesthesia. Patient with one lung not working beyond the stenosis Patient under guardianship Pregnancy 12 months follow-up impossible
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jean-Michel Vergnon, MD PhD
Organizational Affiliation
CHU SAINT-ETIENNE
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of pneumology, CHU Amiens
City
Amiens
Country
France
Facility Name
Departement of pneumology, CHU Brest
City
Brest
Country
France
Facility Name
Pneumology departement, Hôpital Percy
City
Clamart
Country
France
Facility Name
Pneumology departement, CHRU Lille
City
Lille
Country
France
Facility Name
Pneumology departement, CHU Limoges
City
Limoges
Country
France
Facility Name
Pneumology departement, Sainte Marguerite hospital
City
Marseille
Country
France
Facility Name
Pneumology departement, CHU Nantes
City
Nantes
Country
France
Facility Name
Pneumology departement, Saint-Antoine hospital
City
Paris
Country
France
Facility Name
Department of respiratory diseases and allergic, Thoracic Oncology, CHU Reims
City
Reims
Country
France
Facility Name
Pneumology Clinic - Albert Calmette hospital- CHU Rouen
City
Rouen
Country
France
Facility Name
Pneumology departement CHU Saint-Etienne
City
Saint-etienne
ZIP/Postal Code
42055
Country
France
Facility Name
Endoscopy unit, Thoracic surgery department, Foch Hospital
City
Suresnes
Country
France
Facility Name
Departement of pneumology, CHU TOULOUSE
City
Toulouse
Country
France

12. IPD Sharing Statement

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Role of a Silicone Prosthesis to Prevent Airway Obstruction Recurrence in Lung Cancers

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