- Trials with a EudraCT protocol (36)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (2)
36 result(s) found for: Lobectomy.
Displaying page 1 of 2.
EudraCT Number: 2004-002380-24 | Sponsor Protocol Number: TC-021-IM | Start Date*: 2005-12-29 | |||||||||||
Sponsor Name:Nycomed Danmark ApS, International Medical Affairs | |||||||||||||
Full Title: An open randomised, prospective, multi-centre, parallel-group trial to compare efficacy and safety of TachoSil versus standard surgical treatment in patients undergoing pulmonary lobectomy for lung... | |||||||||||||
Medical condition: Management of pulmonary air leakage following lobectomy in subjects with lung malignancies including metastases. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) HU (Completed) DE (Completed) DK (Completed) SE (Completed) BE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-005583-27 | Sponsor Protocol Number: KB 041 | Start Date*: 2008-05-19 | |||||||||||
Sponsor Name:KEDRION | |||||||||||||
Full Title: A multi-center, randomized, prospective, controlled open-label Phase II/III study to assess the safety and sealing efficacy of Kedrion Fibrin Sealant in patients eligible for anatomical pulmonary r... | |||||||||||||
Medical condition: Primary or secondry lung cancer, or other parenchymal disease for which pulmonary resection surgery is indicated 3. Patients eligible for anatomical or atypical pulmonary resection lobe resectio... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-006001-16 | Sponsor Protocol Number: HVF-001-2008 | Start Date*: 2008-12-10 | |||||||||||
Sponsor Name:AZIENDA UNITA` SANITARIA LOCALE LECCE | |||||||||||||
Full Title: Efficacy of TachoSil on air leakage in chest surgery | |||||||||||||
Medical condition: Patient undergone lobectomy or segmentectomy (anatomical segmentectomy) for lung carcinoma and that during intraoperative phase after first suture with stapler show air leakage with grade 1-2 accor... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000397-30 | Sponsor Protocol Number: PLASMAFIST-2011 | Start Date*: 2013-02-07 | |||||||||||
Sponsor Name:FUNDACIÓN CANARIA DE INVESTIGACIÓN Y SALUD (FUNCIS) | |||||||||||||
Full Title: CLINICAL ASSESSMENT OF THE EFFECTS OF AUTOLOGOUS PLATELET-POOR PLASMA ON PREVENTION OF BRONCHOPLEURAL FISTULA AND LUNG DAMAGE IN PATIENTS UNDERGOING LUNG RESECTION SURGERY | |||||||||||||
Medical condition: Bronchopleural fistula | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-000760-18 | Sponsor Protocol Number: 13.034 | Start Date*: 2014-11-24 |
Sponsor Name:Prof. Peter Licht | ||
Full Title: Supplementary Epidural Analgesia in Video-Assisted Thoracic Surgery (VATS) - The SEAVATS Study. | ||
Medical condition: Cancer pulmones | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2006-004713-18 | Sponsor Protocol Number: 01061 | Start Date*: 2006-11-23 | |||||||||||
Sponsor Name:European Lung Cancer Working Party | |||||||||||||
Full Title: A phase II study assessing the curative effect of the combination of lobectomy followed by mediastinal concomitant radiochemotherapy in patients with locally advanced unresectable stage III non-sma... | |||||||||||||
Medical condition: This phase II study aim to determine if radical radiochemotherapy on the mediastinum after lobectomy can be associated with significant long term survival in patients with initially unresectable st... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-000575-27 | Sponsor Protocol Number: MK-3475-091-05 | Start Date*: 2015-09-17 | |||||||||||
Sponsor Name:Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc. | |||||||||||||
Full Title: A randomized, phase 3 trial with anti-PD-1 monoclonal antibody pembrolizumab (MK-3475) versus placebo for patients with early stage NSCLC after resection and completion of standard adjuvant therapy... | |||||||||||||
Medical condition: Stage IB (T ≥ 4 cm), II and IIIA NSCLC | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Trial now transitioned) SI (Trial now transitioned) GB (GB - no longer in EU/EEA) DE (Trial now transitioned) ES (Ongoing) EE (Trial now transitioned) HU (Trial now transitioned) PT (Trial now transitioned) BE (Trial now transitioned) AT (Trial now transitioned) NL (Trial now transitioned) DK (Trial now transitioned) GR (Trial now transitioned) LV (Trial now transitioned) CZ (Trial now transitioned) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-017768-18 | Sponsor Protocol Number: 0908127 | Start Date*: 2010-03-19 | ||||||||||||||||
Sponsor Name:CHU Saint-Etienne | ||||||||||||||||||
Full Title: Analgésie par bloc continu du plan transverse de l’abdomen en chirurgie d’exérèse hépatique : efficacité et influence sur la réhabilitation précoce. | ||||||||||||||||||
Medical condition: hepatectomy or segmentectomy | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-002818-11 | Sponsor Protocol Number: 2003AN004 | Start Date*: 2004-12-08 |
Sponsor Name:Heart of England NHS Foundation Trust | ||
Full Title: Magnesium Sulphate for the Prevention of Super Ventricular Dysrrhythmias following Non-Cardiac Thoracic Surgery | ||
Medical condition: Post Thoracotomy Super Ventricular Dysrhythmias | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2012-002844-25 | Sponsor Protocol Number: 12.006 | Start Date*: 2012-08-13 | ||||||||||||||||
Sponsor Name:Palle Toft | ||||||||||||||||||
Full Title: The effect of Phrenic nerve blokade on acute and chronic shoulder pain in patients for lobectomy and pneumonectomy. | ||||||||||||||||||
Medical condition: Postoperative shoulder pain, after lobectomy and pneumonectomy | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-006525-26 | Sponsor Protocol Number: UNISI-001-2007 | Start Date*: 2008-03-04 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA SENESE | |||||||||||||
Full Title: efficacy of TachoSil on air leakage in chest surgery | |||||||||||||
Medical condition: Patients undergone to lobectomy for non-small cell lung cancer (NSCLC) performed through posterolateral or anterolateral thoracotomy and that during intraoperative phase after first suture with sta... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-006445-18 | Sponsor Protocol Number: 1403/08 | Start Date*: 2010-09-23 | |||||||||||
Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | |||||||||||||
Full Title: Paravertebral block: influence of Body Mass Index on the dosage of local anaesthetic. | |||||||||||||
Medical condition: postoperative pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-001283-73 | Sponsor Protocol Number: 109493 | Start Date*: 2007-08-16 | ||||||||||||||||||||||||||
Sponsor Name:GlaxoSmithKline Biologicals | ||||||||||||||||||||||||||||
Full Title: A double-blind, randomized, placebo-controlled Phase III study to assess the efficacy of recMAGE-A3 + AS15 Antigen-Specific Cancer Immunotherapeutic as adjuvant therapy in patients with resectable ... | ||||||||||||||||||||||||||||
Medical condition: Adjuvant therapy in patients with MAGE-A3-positive Non-Small Cell Lung Cancer (NSCLC) and who have had complete surgical resection | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: BE (Prematurely Ended) DE (Prematurely Ended) IE (Prematurely Ended) FI (Prematurely Ended) ES (Prematurely Ended) SI (Prematurely Ended) FR (Completed) SE (Prematurely Ended) GR (Prematurely Ended) IT (Prematurely Ended) LV (Prematurely Ended) AT (Completed) NL (Prematurely Ended) HU (Prematurely Ended) CZ (Prematurely Ended) EE (Prematurely Ended) GB (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2006-004777-10 | Sponsor Protocol Number: 107240 | Start Date*: 2007-03-14 |
Sponsor Name:GlaxoSmithKline Biologicals | ||
Full Title: A Phase I/II study to assess the safety and immunogenicity of recMAGE-A3+AS15 cancer immunotherapeutic given as adjuvant therapy, with or without standard adjuvant chemo(-radio)therapy, to patients... | ||
Medical condition: Adult patients with pathologically proven MAGE A3-positive Non-Small Cell Lung Cancer in stage IB, II or III. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) BE (Prematurely Ended) DE (Completed) FR (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-002609-31 | Sponsor Protocol Number: ISO-44-013 | Start Date*: 2012-01-27 | |||||||||||
Sponsor Name:Guerbet | |||||||||||||
Full Title: Diagnostic contribution of XENETIX® CT PERFUSION in pre-therapeutical assessment of hepatocellular carcinoma. | |||||||||||||
Medical condition: Subjects diagnosed for HCC and planned for surgery (tumorectomy, sectionectomy, segmentectomy, lobectomy or transplantation). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-004537-16 | Sponsor Protocol Number: MO11/10085 | Start Date*: 2013-01-25 | |||||||||||
Sponsor Name:University of Leeds | |||||||||||||
Full Title: An Open Label Multi-Centre Preoperative Window of Opportunity Study of Afatinib in Stage Ia to IIb Non-Small Cell Lung Cancer | |||||||||||||
Medical condition: Non-small cell lung cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-004451-37 | Sponsor Protocol Number: VATS-SVP | Start Date*: 2012-11-27 | |||||||||||
Sponsor Name:Per F. Jensen | |||||||||||||
Full Title: Multimodal analgesia in video-assisted thoracic surgery with interostal catheter and glucocorticoid - a randomized, double-blind, placebo-controlled study. | |||||||||||||
Medical condition: Pain after thoracoscopic surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-005712-40 | Sponsor Protocol Number: 1253/08 | Start Date*: 2008-09-19 | |||||||||||
Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | |||||||||||||
Full Title: Evaluation of postoperative pain management with thoracic paravertebral block using levobupivacaine associated with sufentanil | |||||||||||||
Medical condition: postoperative pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-001343-31 | Sponsor Protocol Number: 2017/182/HP | Start Date*: 2018-11-27 | |||||||||||
Sponsor Name:CHU-Hôpitaux de Rouen | |||||||||||||
Full Title: Double regional anesthesia in video assisted thoracoscopy | |||||||||||||
Medical condition: Thoracic surgery for pulmonary anatomic resection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-003931-12 | Sponsor Protocol Number: BXU513667 | Start Date*: 2017-12-13 | |||||||||||
Sponsor Name:Baxter Healthcare Corporation | |||||||||||||
Full Title: A Randomized Controlled Non-inferiority Study to Evaluate the Efficacy and Safety of Hemopatch Compared to TachoSil in Preventing or Reducing Postoperative Air Leaks After Pulmonary Resection. | |||||||||||||
Medical condition: Postoperative air leakage. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
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