- Trials with a EudraCT protocol (49)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
49 result(s) found for: Thoracotomy.
Displaying page 1 of 3.
EudraCT Number: 2007-002769-11 | Sponsor Protocol Number: Gabapentin02 | Start Date*: 2010-01-25 | ||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Department of Cardiothoracic and Vascular Surgery | ||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: THE EFFECT OF GABAPENTIN ON THORACIC EPIDURAL ANALGESIA FOLLOWING THORACOTOMY – A RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED TRIAL | ||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: The purpose of this trial is to investigate the effect of gabapentin on thoracic epidural analgesia following thoracotomy, including assessment of both analgesia, pain intensity, pain quality and w... | ||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-001033-24 | Sponsor Protocol Number: 1234 | Start Date*: 2016-01-25 | |||||||||||
Sponsor Name:AOU CITTA' DELLA SALUTE E DELLA SCIENZA DI TORINO | |||||||||||||
Full Title: The management of post-operative pain nia patients undergoing cardiac surgery mini - invasive minithoracotomy : Randomized trial | |||||||||||||
Medical condition: The management of postoperative pain in patients undergoing cardiac surgery minimally invasive minithoracotomy : randomized | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-000506-21 | Sponsor Protocol Number: Chumbley1 | Start Date*: 2011-06-21 |
Sponsor Name:Imperial College Healthcare NHS Trust | ||
Full Title: A double-blind, randomised placebo-controlled trial to determine whether low-dose intravenous ketamine peri-operatively can prevent chronic post-surgical pain, in patients undergoing thoracotomy or... | ||
Medical condition: Chronic post-surgical pain | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-016951-23 | Sponsor Protocol Number: Levo-Fa | Start Date*: 2009-12-02 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA MAGGIORE DELLA CARITA` DI NOVARA | |||||||||||||
Full Title: Thoracic epidural L-Bupivacaine and onset of symptomatic supraventricular tachy-arrhythmias after thoracotomy. | |||||||||||||
Medical condition: patients submitted to a thoracotomy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-003275-19 | Sponsor Protocol Number: 402-C-322 | Start Date*: 2013-01-29 | |||||||||||
Sponsor Name:Pacira Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Phase 3, Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study to Assess the Efficacy and Safety of Intercostal Nerve Block with Liposome Bupivacaine in Subjects Undergo... | |||||||||||||
Medical condition: Intercostal Nerve Block for Posterolateral Thoracotomy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) PL (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-001285-40 | Sponsor Protocol Number: AGO/ANE/04/01 | Start Date*: 2004-10-25 |
Sponsor Name:University Hospital Ghent | ||
Full Title: Wat is de ideale concentratie van Ropivacaine bij Sufenta 0,75 microgram/ml voor Thoracale Epidurale? | ||
Medical condition: Thoracotomy for lung resection | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2007-005544-24 | Sponsor Protocol Number: Sufentanil/Fentanyl in toracotomia | Start Date*: 2007-06-20 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA DI PADOVA | |||||||||||||
Full Title: Sperimental, controlled, randomized single blind study. Sufentanil vs fentanyl in patientes with thoracotomy for pulmonary resection and videolaparoscopic surgery. | |||||||||||||
Medical condition: Patientes with thoracotomy for pulmonary resection and videolaparoscopic surgery. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-016337-10 | Sponsor Protocol Number: KF10004/08 | Start Date*: 2010-04-26 | ||||||||||||||||
Sponsor Name:Grünenthal GmbH | ||||||||||||||||||
Full Title: Lidocaine 5% medicated plaster for the topical treatment of localized chronic postoperative neuropathic pain after total knee replacement or thoracotomy | ||||||||||||||||||
Medical condition: localized chronic post-operative neuropathic pain (PoNP) after total knee replacement or thoracotomy (including drainage, excluding subjects with neoplasia-related thoracotomy) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-001769-14 | Sponsor Protocol Number: LACO15 | Start Date*: 2017-02-13 |
Sponsor Name:Javier E. Morales Sarabia | ||
Full Title: Analgesic efficacy of intravenous lacosamide administered perioperatively for thoracic surgery with thoracotomy approach. | ||
Medical condition: Acute postoperative pain | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2010-021534-55 | Sponsor Protocol Number: 72311424 | Start Date*: 2010-12-16 | |||||||||||
Sponsor Name:Luis Carlos Imaz Navarro | |||||||||||||
Full Title: Comparación analgésica de bupivacaína, a diferentes dosis por catéter paravertebral torácico, y su implicación en la función pulmonar en pacientes intervenidos de toracotomía para cirugía de resecc... | |||||||||||||
Medical condition: Pacientes intervenidos de toracotomía para cirugía de resección pulmonar (Thoracotomy for pulmonar resection) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
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: 2009-011219-20 | Sponsor Protocol Number: 2009/04 | Start Date*: 2009-05-18 | |||||||||||
Sponsor Name:Hopital Foch | |||||||||||||
Full Title: Comparison between two methods of post-operative analgesia after thoracotomy: epidural administration of sufentanil and levobupivacaine and epidural administration of levobupivacaine associated wit... | |||||||||||||
Medical condition: postoperative epidural analgesia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-005062-30 | Sponsor Protocol Number: NF001 | Start Date*: 2015-06-02 |
Sponsor Name:University Hospital Germans Trias i Pujol | ||
Full Title: Randomized, double-blind, placebo controlled clinical trial to assess the phrenic nerve functional status after periphrenic lidocaine infiltration in lung resection surgery. | ||
Medical condition: Ipsilateral shoulder pain after thoracotomy for lung resection. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2005-002148-25 | Sponsor Protocol Number: 04 SG 25 | Start Date*: 2005-10-05 |
Sponsor Name:Great Ormond Street Hospital | ||
Full Title: A double blind randomised control trial of perioperative glutamine administration: a potential therapy for preventing post-operative immune hypo-responsiveness. | ||
Medical condition: Postoperative immune hporesponsiveness | ||
Disease: | ||
Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2013-002000-14 | Sponsor Protocol Number: CM042013 | Start Date*: 2013-07-17 |
Sponsor Name:University Hospitals Leuven | ||
Full Title: The effects of right paravertebral blockade on biventricular performance in patients with chronic pulmonary hypertension scheduled for minimally invasive mirtral valve surgery. | ||
Medical condition: patients with pulmonary hypertension scheduled for elective minimally invasive mitral valve surgery using heartport technique. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2008-001518-26 | Sponsor Protocol Number: DFI10569 | Start Date*: 2009-03-30 | |||||||||||
Sponsor Name:sanofi-aventis recherche & développement | |||||||||||||
Full Title: Efficacy and safety of oral ataciguat (HMR1766) 200 mg administered once daily for 28 days on pain reduction in patients with Neuropathic Pain. A randomized, double-blind, placebo-controlled, cross... | |||||||||||||
Medical condition: The proposed study is planned to demonstrate that ataciguat 200 mg/day could be effective in reducing neuropathic pain with a good safety profile | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) CZ (Completed) DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-004264-19 | Sponsor Protocol Number: NEODEX2 | Start Date*: 2017-04-05 |
Sponsor Name:Uppsala County Council | ||
Full Title: Anesthesia with dexmedetomidine and fentanyl for neonatal surgery. A pilot study. | ||
Medical condition: The state of anesthesia intraoperatively and pain postoperatively | ||
Disease: | ||
Population Age: Newborns, Under 18 | Gender: Male, Female | |
Trial protocol: SE (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2020-003300-14 | Sponsor Protocol Number: 74719 | Start Date*: 2020-10-07 |
Sponsor Name:Department of Cardiothoracic Surgery, Aalborg Universityhospital | ||
Full Title: Botulinum Toxin A as Treatment for Chronic Postsurgical Pain Following Lung Cancer Surgery: a Randomized Controlled Pilot Trial | ||
Medical condition: Post Thoracotomy Pain Syndrome (PTPS) | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: DK (Prematurely Ended) | ||
Trial results: View results |
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 |
EudraCT Number: 2009-012094-35 | Sponsor Protocol Number: D5090C00018 | Start Date*: 2009-08-11 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Phase IIa randomised, double-blind, placebo controlled, parallel group, multicentre study evaluating the efficacy, safety, tolerability and pharmacokinetics of AZD1386 after 3 weeks of treatment... | |||||||||||||
Medical condition: Patients with Posttraumatic Neuralgia (PTN) and Postherpetic Neuralgia (PHN) Intended Indication is Neuropathic Pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) FR (Completed) DK (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
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