Clinical Trials Logo

Thoracotomy clinical trials

View clinical trials related to Thoracotomy.

Filter by:

NCT ID: NCT00867412 Completed - Clinical trials for Non-Small Cell Lung Cancer

Randomized Study of Positron Emission Tomography - Computed Tomography (PET/CT) in Pre-Operative Staging of Lung Cancer

Start date: January 2002
Phase: N/A
Study type: Observational

Patients with possible operable non-small cell lung cancer are randomised to conventional staging, or conventional staging and PET/CT. According to, patients with operable tumor will be referred to surgery, and the number of thoracotomies and futile thoracotomies wil be compared with the two groups in order to asses the possible benefit of PET/CT.

NCT ID: NCT00834769 Completed - Chronic Pain Clinical Trials

Chronic Pain After Thoracotomy, an Incidence Study in a Single Surgical Center

Start date: December 2008
Phase: N/A
Study type: Observational

Investigation of chronic pain frequency after thoracotomy for lung cancer. Risk factors for development of chronic pain are investigated. Questionnaire survey.

NCT ID: NCT00746213 Completed - Chronic Pain Clinical Trials

Chronic Pain After Thoracotomy, an Incidence Study

Start date: July 2008
Phase: N/A
Study type: Observational

This is an investigation on the frequency of chronic pain after thoracotomy for lung cancer. Factors relating to the development of chronic pain are investigated. Questionnaire survey.

NCT ID: NCT00598000 Completed - Lung Cancer Clinical Trials

Quality of Life and Pain Outcomes Following Video-Assisted Thoracic Surgery (VATS) Anatomic Lung Resection Versus Thoracotomy and Anatomic Lung Resection

Start date: February 2005
Phase: N/A
Study type: Observational

The purpose of this study is to see if different types of surgery for lung cancer have different effects on quality of life and pain. What we learn from this study may help us find new ways to improve the quality of life of lung cancer patients who have surgery.

NCT ID: NCT00498251 Completed - Anesthesia Clinical Trials

Prevention of Lung Edema After Thoracic Surgery

Start date: September 2004
Phase: N/A
Study type: Interventional

Background : Acute lung injury (ALI) occasionally occurs after pulmonary resection and carries a bad prognosis with a high mortality rate ranging from 20 to 100%. Objectives : 1. to evaluate pre-, intra- and postoperative changes in hemodynamics, oxygenation indices as well as intra- and extravascular lung water using simple thermodilution technique and continuous arterial pressure analysis 2. to test the efficacy of inhaled beta2 -adrenergic agonist versus anticholinergic agents to reduce lung edema in patients undergoing thoracic surgery and in pigs subjected to lipolysacharide-induced ALI. Design of the research protocol: - Prospective controlled trial including surgical patients with high risk factors for ALI (n=60) allocated to receive inhaled drugs (randomised, double-blind, cross-over mode). - Main measurements: Intra-thoracic blood volume, intra- and extra-vascular lung water, hemodynamic parameters (CO, systolic arterial pressure/flow variations, dPmax, MAP, CVP), oxygenation indices (PaO2/FIO2), ventilatory parameters, clinical outcome data, histochemical and pathological data. Glossary CO = cardiac output; dPmax = maximal arterial pressure slope; SAP-V = systolic arterial pressure variations; Flow–V = Flow variations; MAP = mean arterial pressure; CVP = central venous pressure; PaO2=arterial oxygen pressure; FIO2= oxygen inspiratory fraction

NCT ID: NCT00460668 Completed - Lung Cancer Clinical Trials

The Effect of Post-thoracotomy Pulmonary Rehabilitation on Quality of Life

Start date: April 2007
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the effects of an integrated multidisciplinary rehabilitation program on health related quality of life in the 12 months postoperative period in patients with an elective thoracotomy and to evaluate the effects of the program on general quality of life (SF-36), acute/chronic post-thoracotomy pain, impairment (changes in pulmonary function), disability (exercise capacity) and start to complete recovery (ECOG score of 0 or 1) 12 months postoperatively in patients with an elective thoracotomy.

NCT ID: NCT00224588 Completed - Pain Clinical Trials

KETOR: Effects of Peri Operative Administration of Ketamine on Long Term Post Thoracotomy Pain

Start date: January 2003
Phase: Phase 3
Study type: Interventional

We assessed the effects of the N Methyl aspartate receptor antagonist Ketamine on long-term post thoracotomy pain. We hypothesized that ketamine could prevent supersensitization of the central nervous system involved in this chronic neuropathic pain.