- Trials with a EudraCT protocol (215)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (2)
215 result(s) found for: PCA.
Displaying page 1 of 11.
EudraCT Number: 2014-004088-19 | Sponsor Protocol Number: TCI-PCA-002 | Start Date*: 2014-12-12 | |||||||||||
Sponsor Name:Universitätsklinikum Erlangen | |||||||||||||
Full Title: Postoperative pain treatment after elective cardiac surgery using patient-controlled target-controlled infusion (TCI-PCA) with hydromorphone vs. patient-controlled analgesia (PCA) with morphine | |||||||||||||
Medical condition: Postoperative pain treatment after elective cardiac surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-001201-10 | Sponsor Protocol Number: FEN-PPA-401 | Start Date*: 2004-07-26 | |||||||||||
Sponsor Name:JANSSEN-CILAG | |||||||||||||
Full Title: Comparison of transdermal fentanyl PCA and IV morphine PCA in the management of post-operative pain control. | |||||||||||||
Medical condition: Treatment of moderate to severe post-operative pain in subjects who have undergone an elective major abdominal or orthopaedic surgical procedure. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-002814-38 | Sponsor Protocol Number: SP005 | Start Date*: 2013-09-27 | |||||||||||
Sponsor Name:SOTIO a.s. | |||||||||||||
Full Title: A Randomized, Double Blind, Multicenter, Parallel-group, Phase III study to evaluate efficacy and safety of DCVAC/PCa versus Placebo in Men with metastatic Castration Resistant Prostate Cancer elig... | |||||||||||||
Medical condition: metastatic castrate-resistant prostate cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: SE (Completed) GB (Completed) DE (Completed) BE (Completed) CZ (Completed) IT (Completed) NL (Completed) ES (Completed) HU (Completed) PT (Completed) BG (Completed) SK (Completed) PL (Completed) HR (Completed) AT (Completed) LV (Completed) LT (Completed) DK (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-004967-65 | Sponsor Protocol Number: SP004 | Start Date*: 2012-01-11 | |||||||||||
Sponsor Name:SOTIO a.s. | |||||||||||||
Full Title: Randomized, open-label, parallel-group, multi-centre phase II clinical trial with active cellular immunotherapy DCVAC/PCa in patients with localized high-risk prostate cancer after primary radiothe... | |||||||||||||
Medical condition: localized high-risk prostate cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-000529-20 | Sponsor Protocol Number: FENHYDPAI4012 | Start Date*: 2008-05-20 |
Sponsor Name:Janssen-Cilag Limited | ||
Full Title: Comparison of Ionsys® and routine care with morphine IV PCA in the management of early post-operative mobilisation, ability to mobilise and in time to Fitness For Discharge (FFD) | ||
Medical condition: Evaluation of the mobilisation characteristics, clinical use, safety and Ease of Care (EOC) of a Fentanyl Iontophoretic Transdermal PCA system (Ionsys) and morphine IV PCA for management of acute... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2005-002848-25 | Sponsor Protocol Number: CN145-010 | Start Date*: 2006-02-28 |
Sponsor Name:Bristol-Myers Squibb SL | ||
Full Title: Protocol Title: A Phase IV, Multi-Center, Randomized, Double-Blind, Placebo- Controlled Study to Evaluate The Analgesic Efficacy And Safety of IV Paracetamol Versus Placebo in subjects with postope... | ||
Medical condition: Pain | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-003302-24 | Sponsor Protocol Number: ESTEVE-SIGM-201 | Start Date*: 2011-11-17 |
Sponsor Name:Laboratorios Dr. Esteve S.A. (ESTEVE) | ||
Full Title: An exploratory, randomized, double blind, placebo controlled, parallel groups Phase II clinical trial to evaluate the efficacy and safety of E-52862 (400 mg) by oral route, as part of an analgesic ... | ||
Medical condition: post-operative pain following abdominal hysterectomy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-010883-40 | Sponsor Protocol Number: META-KETA | Start Date*: 2009-10-02 |
Sponsor Name:IMAS | ||
Full Title: Efecto de la administración endovenosa combinada de metadona y ketamina en PCA sobre la analgesia postoperatoria de pacientes intervenidos de artrodesis lumbar. | ||
Medical condition: Dolor postoperatorio tras artrodesis lumbar | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2006-004349-41 | Sponsor Protocol Number: ANA06103 | Start Date*: 2007-01-18 |
Sponsor Name:Universitätsklinikum Mannheim, Klinik für Anästhesiologie | ||
Full Title: Supportive Schmerztherapie-Studie - Einfluss von Physostigmin auf die patientenkontrollierte Analgesie (PCA) in der postoperativen Phase bei Intensivpatienten | ||
Medical condition: In der vorliegenden Studie soll untersucht werden, ob die Supplementierung einer patientenkontrollierten Analgesie (PCA) mit Piritramid (Dipidolor) durch Physostigmin (Anticholium®) in der postoper... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2019-000596-16 | Sponsor Protocol Number: DH112018 | Start Date*: 2019-04-17 |
Sponsor Name:University Hospitals Leuven | ||
Full Title: Erector spinae plane block for minimal invasive direct coronary artery bypass surgery. A double blind, prospective randomized placebo-controlled trial. | ||
Medical condition: postoperative pain | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-001125-27 | Sponsor Protocol Number: DH022019 | Start Date*: 2019-06-04 |
Sponsor Name:University Hospitals Leuven | ||
Full Title: Erector Spinae plane block for minimal invasive mitral valve surgery. A double blind, prospective randomized placebo-controlled trial. | ||
Medical condition: postoperative pain | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-004094-25 | Sponsor Protocol Number: EGD-EC-003 | Start Date*: 2006-01-05 | |||||||||||
Sponsor Name:Astellas Pharma Europe B.V. | |||||||||||||
Full Title: A phase IIIb randomized study of intermittent versus continuous androgen deprivation therapy using ELIGARD 22.5 mg 3-month depot in subjects with relapsing or locally advanced prostate cancer who a... | |||||||||||||
Medical condition: Histologically or cytologically confirmed adenocarcinoma of the prostate (PCa) meeting the following criteria: - Locally adv. (stage T3 or T4) PCa, N0 or N+, M0 with PSA >= 5 ng/ml, or - Relapsing ... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: CZ (Completed) AT (Prematurely Ended) FI (Completed) SK (Completed) IE (Completed) HU (Completed) DE (Completed) ES (Completed) SE (Completed) GB (Completed) PT (Completed) BE (Completed) DK (Completed) GR (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-005424-33 | Sponsor Protocol Number: 17308 | Start Date*: 2008-02-06 |
Sponsor Name:Sint Lucas Andreas | ||
Full Title: Epidural analgesia versus Remifentanil PCA during labour | ||
Medical condition: To compare Remifentanil PCA with epidural anesthesia among healthy nulligravidia during labor. | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2009-013803-70 | Sponsor Protocol Number: 01/2009 | Start Date*: 2009-12-28 |
Sponsor Name:Splošna bolnišnica Celje | ||
Full Title: Modified PCA regimen of remifentanil delivery for labour pain Prilagojeno od porodnice vodeno lajšanje porodne bolečine z remifentanilom | ||
Medical condition: pregnancy, labour, labour pain | ||
Disease: | ||
Population Age: In utero, Preterm newborn infants, Newborns, Under 18, Adults | Gender: Female | |
Trial protocol: SI (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2017-002651-28 | Sponsor Protocol Number: IRST185.05 | Start Date*: 2018-02-22 | |||||||||||
Sponsor Name:ISTITUTO SCIENTIFICO ROMAGNOLO PER LO STUDIO E LA CURA DEI TUMORI (IRST) S.R.L. IRCCS | |||||||||||||
Full Title: Multi-cohort investigational study to evaluate the impact of pelvic mp-3TMRI and whole-body 68Ga-PSMA PET/CT for diagnosis of clinically-significant prostate cancer and pre-surgical staging. | |||||||||||||
Medical condition: prostate cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-005257-22 | Sponsor Protocol Number: RG_12-151 | Start Date*: 2013-07-12 |
Sponsor Name:University of Birmingham | ||
Full Title: Remifentanil intravenous patient controlled analgesia (PCA) versus intramuscular pethidine for pain relief in labour: a randomised controlled trial | ||
Medical condition: Childbirth | ||
Disease: | ||
Population Age: | Gender: Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-000194-31 | Sponsor Protocol Number: PenCTU/2010/CTIMP-004 | Start Date*: 2011-05-20 |
Sponsor Name:Plymouth Hospitals NHS Trust | ||
Full Title: An open randomised trial of patient controlled analgesia (PCA) versus routine care in the Emergency Department | ||
Medical condition: Patients presenting to the Emergency Department in severe pain from either musculoskeletal injury or non-traumatic abdominal pain. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-004735-32 | Sponsor Protocol Number: SP001 | Start Date*: 2012-01-11 | |||||||||||
Sponsor Name:SOTIO a.s. | |||||||||||||
Full Title: Randomized, open-label, parallel-group, multi-centre phase II clinical trial with active cellular immunotherapy DCVAC/PCa in patients with castrate-resistant prostate cancer | |||||||||||||
Medical condition: metastatic castrate-resistant prostate cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-004986-34 | Sponsor Protocol Number: SP002 | Start Date*: 2012-01-11 | |||||||||||
Sponsor Name:SOTIO a.s. | |||||||||||||
Full Title: Randomized, open-label, parallel-group, multi-centre phase II clinical trial with active cellular immunotherapy DCVAC/PCa in combination with hormone therapy in patients with metastatic prostate ca... | |||||||||||||
Medical condition: metastatic prostate cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-004985-14 | Sponsor Protocol Number: SP003 | Start Date*: 2012-01-11 |
Sponsor Name:Sotio a.s. | ||
Full Title: Randomized, open-label, parallel-group, multi-centre phase II clinical trial of active cellular immunotherapy DCVAC/PCa in patients with localized prostate cancer after primary radical prostatectomy | ||
Medical condition: Localized prostate cancer after primary radical prostatectomy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: CZ (Completed) | ||
Trial results: View results |
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