- Trials with a EudraCT protocol (454)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (2)
454 result(s) found for: Chest pain.
Displaying page 1 of 23.
EudraCT Number: 2021-002288-24 | Sponsor Protocol Number: Ci-FCP001 | Start Date*: 2021-08-10 |
Sponsor Name:Amsterdam UMC | ||
Full Title: Effect of citalopram on chest pain in patients with functional chest pain | ||
Medical condition: Chest pain can be divided in cardiac or non-cardiac chest pain (NCCP). To establish the diagnosis NCCP, acute coronary disease has to be ruled out first. NCCP can be caused by functional chest pain... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2011-002630-39 | Sponsor Protocol Number: 3tcAZ | Start Date*: 2011-10-25 |
Sponsor Name:Oslo University Hospital Rikshospitalet | ||
Full Title: MICROVASCULAR RESISTANCE IN WOMEN WITH CHEST PAIN AND NO OR MINIMAL CORONARY ARTERY DISEASE | ||
Medical condition: Investigation of otherwise healthy women with chest pain without significant stenoses in their epicardial coronary arteries. | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: NO (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2008-003596-46 | Sponsor Protocol Number: 942/08 | Start Date*: 2009-02-25 | ||||||||||||||||
Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | ||||||||||||||||||
Full Title: Multicenter, not-for-profit clinical study, in a open, controlled, randomized fashion to compare tolerability, safety and efficacy of two different treatment strategies for non malignant, persisten... | ||||||||||||||||||
Medical condition: non neoplastic cronic pain | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-001202-14 | Sponsor Protocol Number: CiPA001 | Start Date*: 2019-06-05 |
Sponsor Name:Amsterdam UMC | ||
Full Title: CiPA Trial: Effect of Citalopram on chest pain in patients with achalasia | ||
Medical condition: Achalasia is a motility disorder of the esophagus. Disappearance of myenteric neurons in the esophageal wall leads to failure of relaxation of the lower esophageal sphincter (LES) and impaired peri... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) | ||
Trial results: (No results available) |
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: 2007-007595-42 | Sponsor Protocol Number: | Start Date*: 2008-04-22 |
Sponsor Name:Cardiac Reserch Unit | ||
Full Title: Chest pain or other pain raising suspicion of an acute coronary syndrome. An evaluation of benzodiazipines and prehospital care. | ||
Medical condition: This study evaluates the possibility to improve symptoms prior to hospital admission among patients suffering from acute chest pain. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2007-000969-37 | Sponsor Protocol Number: AN-SCD1121 | Start Date*: 2007-10-05 | |||||||||||
Sponsor Name:Anthera Pharmaceuticals Incorporated | |||||||||||||
Full Title: IMPACTS Trial: Investigation of the Modulation of Phospholipase in Acute Chest Syndrome (Dose Escalation Study: Varespladib Infusion [A-001] for the Prevention of Acute Chest Syndrome in At-Risk ... | |||||||||||||
Medical condition: Acute Chest Syndrome (ACS) in At-Risk patients with Sickle Cell Disease (SCD) and Vaso-occlusive Crisis (VOC) | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-005226-31 | Sponsor Protocol Number: 1.1 | Start Date*: 2006-04-24 |
Sponsor Name:University of Oxford, Nuffield Department of Medicine | ||
Full Title: TIME 1 The First Therapeutic Intervention in Malignant Pleural Effusion Trial (TIME1) A 2 x 2 randomised factorial trial to assess whether non-steroidal anti-inflammatory analgesics and small bore... | ||
Medical condition: Malignant pleural effusion | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-001860-22 | Sponsor Protocol Number: CRT | Start Date*: 2007-06-04 |
Sponsor Name:Karl Andersen | ||
Full Title: CREATE. Cardiovascular Risk Evaluation and Attenuation of inflammation by early rosuvastatin TrEatment | ||
Medical condition: Patients with chest pain at rest or minimal physical activity of at least 20 minutes duration will be considered for inclusion in this study. To be eligible, patients have to be considered of low... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IS (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: 2006-000540-98 | Sponsor Protocol Number: 2005/495-31 | Start Date*: 2006-04-10 |
Sponsor Name:Karolinska University Hospital | ||
Full Title: Substudie Bröstmärta provocerad med iv bolus adenosin injektion i huvudstudie: Jämförelse mellan aktiv och passiv fysisk träning för behandling av persisterande angina pectoris - en randomiserad st... | ||
Medical condition: Refractory angina pectoris. Testing of sensitivity of chest pain provoked by iv bolus of adenosin before and after a training period with EECP (Enhanced External Counterpulsation) or physical exerc... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2007-002293-54 | Sponsor Protocol Number: Apex01version6 | Start Date*: 2007-11-29 |
Sponsor Name:University of Dundee | ||
Full Title: The APEX Trial: Effects of Allopurinol on Coronary and Peripheral Endothelial Function in Patients with Cardiac Syndrome X | ||
Medical condition: Patients with cardiac syndrome X (typical anginal-like chest pain and normal coronary arteriograms) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-015659-26 | Sponsor Protocol Number: 2009-015659-26 | Start Date*: 2010-01-22 | |||||||||||||||||||||
Sponsor Name:Karolinska Institutet | |||||||||||||||||||||||
Full Title: Cortical and hormonal stress responses to pain management with morphine in standard clinical dosage | |||||||||||||||||||||||
Medical condition: Neonatal pain | |||||||||||||||||||||||
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Population Age: Preterm newborn infants, Newborns, Under 18 | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: SE (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
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: 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: 2020-004584-11 | Sponsor Protocol Number: 10140021910007 | Start Date*: 2021-02-03 | |||||||||||
Sponsor Name:Maxima MC | |||||||||||||
Full Title: Optimal postoperative Pain management After Lung surgery (OPtriAL): multi-centre randomised trial | |||||||||||||
Medical condition: Acute postoperative pain after lung surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-021955-14 | Sponsor Protocol Number: BUP3030 | Start Date*: 2011-10-17 | ||||||||||||||||
Sponsor Name:Purdue Pharma L.P. | ||||||||||||||||||
Full Title: A Multicenter, Inpatient, Open-label Study to Characterize the Pharmacokinetics, Safety, and Efficacy of Intravenous Dosing of Buprenorphine in Pediatric Patients Aged from Birth to 6 Years of Age... | ||||||||||||||||||
Medical condition: Acute moderate to severe pain requiring opioids for at least 24 hours in postoperative and prolonged endotracheal intubated patients | ||||||||||||||||||
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Population Age: Newborns, Infants and toddlers, Children, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: HU (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-017664-16 | Sponsor Protocol Number: 200905-02 | Start Date*: 2010-03-22 |
Sponsor Name:BIOTRONIK France | ||
Full Title: GIANT Study - Genotyping Infarct patients to Adjust and Normalize Thienopyridine treatment | ||
Medical condition: The GIANT trial is dedicated to STEMI patients being treated by a primary PCI (with stent implantation) within the 24 hours following the first pain. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2010-024462-21 | Sponsor Protocol Number: Reda 007583 | Start Date*: 2011-04-26 |
Sponsor Name:Research and Development, Barts and The London NHS Trust | ||
Full Title: Prospective, double-blinded, randomised, placebo controlled trial of pre-emptive analgesia to prevent pain following sternotomy for cardiac surgery. | ||
Medical condition: Chronic pain in the chest incision site (sternotomy) after cardiac surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-003722-26 | Sponsor Protocol Number: SBH-TNF-01 | Start Date*: 2006-03-01 |
Sponsor Name:Barts and the London NHS Trust | ||
Full Title: A prospective, single centre, randomised, double-blind, placebo controlled trial to assess the analgesic effects of one week treatment with anti-TNF in patients with lower back and leg pain. | ||
Medical condition: Lower back and leg pain | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Temporarily Halted) | ||
Trial results: View results |
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