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Fast Track Rehabilitation Following Video-assisted Lung Segmentectomy

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01397045
First Posted: July 19, 2011
Last Update Posted: March 28, 2014
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
Nikolaos Barbetakis, Theagenio Cancer Hospital
July 14, 2011
July 19, 2011
March 28, 2014
July 2011
March 2014   (Final data collection date for primary outcome measure)
Duration of hospital stay [ Time Frame: Participants will be followed till home discharge, an average of 2 weeks ]
Same as current
Complete list of historical versions of study NCT01397045 on ClinicalTrials.gov Archive Site
postoperative morbidity [ Time Frame: Participants will be followed till home discharge, an average of 2 weeks ]
Same as current
Not Provided
Not Provided
 
Fast Track Rehabilitation Following Video-assisted Lung Segmentectomy
Not Provided
Aim of this prospective randomized study is to assess the safety and efficacy of video-assisted lung segmentectomy (Group B) comparing with mini muscle-sparing thoracotomy (group A) during diagnostic process for pulmonary nodules.
Not Provided
Interventional
Not Provided
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single (Participant)
Primary Purpose: Diagnostic
Multiple Pulmonary Nodules
  • Other: VATS
    Video-assisted lung segmentectomy
  • Procedure: Mini thoracotomy
    Mini muscle sparing thoracotomy for lung segmentectomy
  • Active Comparator: Video-assisted lung segmentectomy
    Patients undergoing VATS segmentectomy
    Intervention: Other: VATS
  • Mini thoracotomy
    Patients undergoing lung segmentectomy through a mini thoracotomy
    Intervention: Procedure: Mini thoracotomy
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
120
March 2014
March 2014   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • Patients with undiagnosed multiple pulmonary nodules

Exclusion Criteria:

  • Centrally located lesions
  • previous thoracotomy
  • extensive lung consolidation, and inability to achieve one lung ventilation
Sexes Eligible for Study: All
up to 80 Years   (Child, Adult, Senior)
No
Contact information is only displayed when the study is recruiting subjects
Greece
 
 
NCT01397045
Theagenio Thoracic Surgery 1
Not Provided
Not Provided
Not Provided
Nikolaos Barbetakis, Theagenio Cancer Hospital
Theagenio Cancer Hospital
Not Provided
Not Provided
Theagenio Cancer Hospital
March 2014

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP