LungSco01: Medicoeconomic Evaluation of Two Surgical Techniques for Lobectomy in the Lung Cancer

Sponsor
Centre Hospitalier Universitaire Dijon (Other)
Overall Status
Terminated
CT.gov ID
NCT02502318
Collaborator
(none)
261
15
2
17.4

Study Details

Study Description

Brief Summary

This is a national study that involves the participation of 600 lung cancer patients indicated that treatment is ablation of the pulmonary lobe. This technique is called lobectomy.

Lobectomy may be performed in two different ways:
  • Thoracotomy, which is the first reference approach and that is to make a large incision in the chest to pass between the ribs and spread the order to ablate the lobe.

  • By video-thoracoscopy, which is a new surgical approach consisting in practice several small incisions in the chest wall to allow the introduction of a camera and special instruments to ablate the lobe.

The mini-invasive nature of video-thoracoscopy has a positive impact on postoperative expectoration and ventilation. As a result, the incidence of postoperative respiratory complications including atelectasis, pneumonia and Acute Respiratory Distress Syndrome (ARDS) is reduced. These respiratory complications are responsible for prolonged stays in Intensive Care Unit (ICU) and overall hospitalisation. It also has an impact on recovery and quality of life when patients return home. The reduction in the incidence of complications should counterbalance the additional cost of video-thoracoscopy.

This study aims to evaluate the effectiveness of these two techniques in relation to the quality of life and the costs they generate.

Patients who agree to participate in the study were assigned to one or other of these groups (technical thoracotomy or video-thoracoscopy technique) by lot.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Video-thoracoscopy
  • Procedure: thoracotomy
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
261 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
Medicoeconomic Analysis of Lobectomy Using Thoracoscopy vs Thoracotomy for Lung Cancer: a Multicentric Randomized Controlled Trial.
Actual Study Start Date :
Jul 29, 2015
Actual Primary Completion Date :
Oct 8, 2021

Arms and Interventions

Arm Intervention/Treatment
Experimental: Lobectomy using video-thoracoscopy

Procedure: Video-thoracoscopy

Active Comparator: Lobectomy using thoracotomy

Procedure: thoracotomy

Outcome Measures

Primary Outcome Measures

  1. The postoperative respiratory complications [30 days after surgery]

  2. An incremental cost-utility ratio associated with the use of Video-Assisted Thoracic Surgery when compared with thoracotomy evaluated using the quality of life questionnary EQ-5D [3 months after surgery]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patients who have given their consent

  • Any patient with proven or suspected lung cancer treated by lobectomy.

  • Patients with a negative mediastinoscopy or negative " EBUS-EUS " following a PET scan showing uptake in mediastinal lymph nodes in the preoperative examination.

  • Age between 18 and 80 years

  • Patient affiliated to a social security regimen

  • Patients with a WHO performance status equal to 0 or 1.

Exclusion Criteria:
  • Adults under wardship

  • Pregnant or breast-feeding women

  • Tumours in contact with the pulmonary artery or developing in the lobar bronchi after bronchial fibroscopy.

  • Tumours in contact with the costal periosteum or invading the chest wall

  • Tumours invading the mediastinal pleura or structures of the mediastinium (superior vena cava, trachea, the main-stem bronchi, aorta, oesophagus, vertebrae)

  • Tumours invading the diaphragm

  • Tumours invading the neurovascular structures of the apex (brachial plexus, subclavicular artery, subclavicular vein) causing Pancoast-Tobias syndrome

  • Patients with histologically-proven contralateral or supraclavicular lymph node (N3) involvement whatever the harvesting method.

  • Patients with a positive mediastinoscopy or positive "EBUS-EUS" following a "PET scan" with uptake in one or more mediastinal lymph nodes.

  • Patients with metastasis (brain, bone, liver, adrenal glands, contralateral lung, pleura).

  • Patients who have undergone neo-adjuvant chemotherapy and/or radiotherapy.

  • Patients included in a neo-adjuvant chemotherapy and/or radiotherapy protocol.

  • Patients who have already undergone thoracotomy.

  • Patients with decompensated heart failure or with a systolic ejection fraction below 30%.

  • Patients with severe pulmonary artery hypertension.

  • Patients with untreated valve disease.

  • Patients with unstable angina despite appropriate treatment.

  • Patients with untreated carotid stenosis greater than 70%.

  • Patients with histologically proven cirrhosis with various decompensations or who have presented haemoptysis because of oesophageal varicose veins.

  • Patients with severe neurological sequellae (hemiplegia, paraplegia, tetraplegia).

  • Patients presenting severe psychiatric disorders (dementia, psychosis).

Contacts and Locations

Locations

Site City State Country Postal Code
1 CHU Amiens Amiens France 80000
2 CH Victor Dupouy Argenteuil France
3 CH Avignon Avignon France
4 Centre Jean Perrin - Clermont-Ferrand Clermont-Ferrand France 63000
5 CHU Dijon Dijon France 21079
6 HCL - Louis Pradel Lyon France
7 APHM Hôpital Nord Marseille France 13015
8 CHU de Montpellier Montpellier France 34295
9 CHU de Nice - Hôpital Pasteur Nice France 06000
10 APHP Hôpital Cochin Paris France 75014
11 APHP Hôpital de Tenon Paris France 75020
12 CHU de Poitiers Poitiers France 86021
13 CHU de Rennes - Hôpital de Pontchaillou Rennes France 35000
14 CHU de Rouen Rouen France 76031
15 HUS Strasbourg - Nouvel Hôpital Civil Strasbourg France 67000

Sponsors and Collaborators

  • Centre Hospitalier Universitaire Dijon

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Centre Hospitalier Universitaire Dijon
ClinicalTrials.gov Identifier:
NCT02502318
Other Study ID Numbers:
  • BERNARD PRME 2014
First Posted:
Jul 20, 2015
Last Update Posted:
Jan 20, 2022
Last Verified:
Jan 1, 2022
Keywords provided by Centre Hospitalier Universitaire Dijon
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 20, 2022